Sant Pau - Institut de Recerca

Principales líneas de investigación

Enfermedades neuromusculares inmunomediadas

Caracterización de nuevos antígenos diana en Myasthenia Gravis y neuropatías inmunomediadas (CIDP, GBS, NMM). Utilización como biomarcadores diagnósticos y terapéuticos.
Patogénesis de nuevos antígenos paranodales en CIDP.
Análisis de la inmunidad innata en miopatías inflamatorias.
Anáisis del impacto de nuevas terapias modulares en enfermedades neuromusculares mediadas por IgG4.
Aspectos funcionales de las células del sistema inmunitario (respuesta a ligandos, producción de anticuerpos, etc.).
Base de datos IGOS para el síndrome de Guillain Barré.
Registro español NMD-ES para enfermedades neuromusculares.

Distrofia muscular, disferlinopatía y miopatías distales

Análisis de MRI muscular como biomarcador para varias distrofias musculares.
Estudio de los perfiles de miRNA y secretoma muscular en distrofias musculares.
Estudio del rol de PDGF en fibrosis de distrofias musculares.
Historia natural de las disferlinopatías. Estudio de resultados clínicos de la Jain Foundation.
Evaluación de la frecuencia de portadores de mutaciones en el gen diferlina en la población normal.

Esclerosis lateral amiotrófica

Epidemiología de ELA en Cataluña.
Perfil genético de pacientes de ELA en España.
Perfil de biomarcadores en diferentes fenotipos de ELA.

Retos

Incrementar el conocimiento de los mecanismos inmunológicos involucrados en la patogénesis de enfermedades neuromusculares autoinmunitarias (MG, CIDP, NMM).
Incrementar el conocimiento de los mecanismos patogénicos en miopatías inflamatorias (DM, PM, IBM).
Buscar nuevos antígenos y desarrollar tests diagnósticos con nuevos biomarcadores en neuropatías mediadas por el sistema inmunitario y Myasthenia Gravis.
Implementar nuevos métodos diagnósticos y de seguimiento de la enfermedad por distrofias musculares resultantes de la disferlinopatía y otras miopatías (biomarcadores – miRNA, secretoma-. MRI, etc.).
Incrementar el conocimiento de los mecanismos patogénicos involucrados en la distrofia muscular resultante de la deficiencia en disferlina y otras distrofias musculares.
Acceso a la sala limpia para manipular células para su uso en humanos.
Utilización del registro NMD.ES para desarrollar investigación en varias enfermedades neuromusculares.

Información adicional : Neuromuscularbcn

Coordinación del grupo

OLIVE PLANA, MONTSERRAT FGS
molive@santpau.cat

Miembros

Blanco Soto, Rosa Maria IR
Carbayo Viejo, Alvaro FGS
Collet Vidiella, Roger IR
Cortes Vicente, Elena FGS
Diaz Manera, Jorge Alberto FGS
Domenech Garcia, Roger IR
Gallardo Vigo, Eduard IR
Guardiola Ripoll, Maria CIBERER
Llanso Caldentey, Laura IR
Llarch Cegarra, Paula IR
Lleixa Rodriguez, Maria Cinta IR
Martin Aguilar, Lorena FGS
Pascual Goñi, Elba FGS
Querol Gutierrez, Luis Antonio FGS
Rocaspana Codana, Josep IR
Rojas Garcia, Ricardo FGS
Segovia Simon, Sonia IR
Tejada Illa, Clara IR
Turon Sans, Joana FGS
Vesperinas Castro, Ana IR
Vidal Fernandez, Maria Nuria IR

Publicaciones 2022

(JIF 2022)

Alonso J, Carrasco A, Borrell M, Fernandez E, Pinol P, Badimon L, Wollin L, Lleixa C, Gallardo E, Olive M, Diaz J, Suarez X. Nintedanib Reduces Muscle Fibrosis and Improves Muscle Function of the Alpha-Sarcoglycan-Deficient Mice. Biomedicines. 2022; 10(10):2629. DOI:10.3390/biomedicines10102629. PMID:36289891. IF:4,7 (Q1/3D). Document type: Article.
Alonso J, Gonzalez L, Bruno C, Panicucci C, Alavi A, Nafissi S, Nilipour Y, Zanoteli E, Isihi LMD, Melegh B, Hadzsiev K, Muelas N, Vilchez JJ, Dourado ME, Kadem N, Kutluk G, Umair M, Younus M, Pegorano E, Bello L, Crawford TO, Suarez X, Topf A, Guglieri M, Marini C, Gallano P, Straub V, Diaz J. Clinical and genetic spectrum of a large cohort of patients with delta-sarcoglycan muscular dystrophy. 2022; 145(2). DOI:10.1093/brain/awab301. PMID:34515763. IF:14,5 (Q1/1D). Document type: Article.
Alonso J, Hernandez JCD, Perez H, Mendoza MD, Gutierrez AJ, Hadjigeorgiou I, Monton F, Gonzalez L, Alonso A, Suarez X, Diaz J. Clinical and genetic features of a large homogeneous cohort of oculopharyngeal muscular dystrophy patients from the Canary Islands. EUROPEAN JOURNAL OF NEUROLOGY. 2022; 29(5). DOI:10.1111/ene.15252. PMID:35112761. IF:5,1 (Q1/2D). Document type: Article.
Alvarez R, Nunez CA, Alonso J, Gallardo E, Collet R, Reyes D, Pascual E, Martin L, Caballero M, Carbayo A, Llauger J, Diaz J, Olive M. High prevalence of paraspinal muscle involvement in adults with McArdle disease. MUSCLE & NERVE. 2022; 65(5). DOI:10.1002/mus.27523. PMID:35174518. IF:3,4 (Q2/5D). Document type: Article.
Blasco L, Costa M, Leno J, Bernal S, Alias L, Codina M, Martinez D, Castiglioni C, Bertini E, Travaglini L, Millan JM, Aller E, Sotoca J, Juntas R, Hoei CE, Moreno A, Guillen E, Costa L, Munell F, Boronat S, Rojas R, Povedano M, Cusco I, Tizzano EF. Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G > C Variant in SMN2. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2022; 23(15):8289. DOI:10.3390/ijms23158289. PMID:35955418. IF:5,6 (Q1/3D). Document type: Article.
Bolano C, Diaz J. Therapeutic Options for the Management of Pompe Disease: Current Challenges and Clinical Evidence in Therapeutics and Clinical Risk Management. Therapeutics and Clinical Risk Management. 2022; 18. DOI:10.2147/TCRM.S334232. PMID:36536827. IF:2,8 (Q3/6D). Document type: Review.
Bullich G, Matalonga L, Pujadas M, Papakonstantinou A, Piscia D, Tonda R, Artuch R, Gallano P, Garrabou G, González JR, Grinberg D, Guitart M, Laurie S, Lázaro C, Luengo C, Martí R, Milà M, Ovelleiro D, Parra G, Pujol A, Tizzano E, Macaya A, Palau F, Ribes A, Pérez LA, Beltran S, Schlüter A, Rodriguez A, Cáceres A, Nascimento A, García À, Cueto A, Marcé A, NELLOAR, Martínez A, et al. [Díaz-Manera J, Rojas-García R, Bernal S, Boronat S]. Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases. JOURNAL OF MOLECULAR DIAGNOSTICS. 2022; 24(5). DOI:10.1016/j.jmoldx.2022.02.003. PMID:35569879. IF:4,1 (Q2/3D). Document type: Article.
Caballero M, Álvarez R, Moga E, Rojas R, Turon J, Querol L, Olivé M, Reyes D, Illa I, Gallardo E, Cortés E. Rituximab in myasthenia gravis: efficacy, associated infections and risk of induced hypogammaglobulinemia. NEUROMUSCULAR DISORDERS. 2022; 32(8). DOI:10.1016/j.nmd.2022.06.006. PMID:35811274. IF:2,8 (Q3/6D). Document type: Article.
Carrasco A, Fernandez E, Suarez X, Pinol P, Alonso J, de Luna N, Schoser B, Meinke P, Dominguez C, Hernandez A, Paradas C, Rivas E, Illa I, Olive M, Gallardo E, Diaz J. BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients. AMERICAN JOURNAL OF PATHOLOGY. 2022; 192(8). DOI:10.1016/j.ajpath.2022.05.003. PMID:35605642. IF:6 (Q1/2D). Document type: Article.
Cortes E, Alvarez R, Pla F, Rojas R, Paradas C, Sevilla T, Casasnovas C, Gomez MT, Pardo J, Ramos A, Pelayo AL, Gutierrez G, Turon J, de Munain AL, Guerrero A, Jerico I, Martin MA, Mendoza MD, Moris G, Velez B, Garcia T, Pascual E, Reyes D, Illa I, Gallardo E. Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome. Annals of Clinical and Translational Neurology. 2022; 9(2). DOI:10.1002/acn3.51492. PMID:35080153. IF:5,3 (Q1/2D). Document type: Article.
Doets AY, Lingsma HF, Walgaard C, Islam B, Papri N, Davidson A, Yamagishi Y, Kusunoki S, Dimachkie MM, Waheed W, Kolb N, Islam Z, Mohammad QD, Harbo T, Sindrup SH, Chavada G, Willison HJ, Casasnovas C, Bateman K, Miller JAL, van den Berg B, Verboon C, Roodbol J, Leonhard SE, Benedetti L, Kuwabara S, van den Bergh P, Monges S, Marfia GA, Shahrizaila N, et al. [Querol L]. Predicting Outcome in Guillain-Barré Syndrome International Validation of the Modified Erasmus GBS Outcome Score. 2022; 98(5). DOI:10.1212/WNL.0000000000013139. PMID:34937789. IF:9,9 (Q1/1D). Document type: Article.
Dominguez C, Diaz C, Juntas R, Nascimiento A, Rivera A, Diaz J. Survey on the management of Pompe disease in routine clinical practice in Spain. Orphanet Journal of Rare Diseases. 2022; 17(1):426. DOI:10.1186/s13023-022-02574-5. PMID:36471448. IF:3,7 (Q2/4D). Document type: Article.
Dominguez C, Fernandez R, Moore U, de la Hoz CPDF, Velez B, Cabezas JA, Alonso J, Gonzalez L, Olive M, Garcia J, Moris G, Hernandez JCL, Muelas N, Servian E, Martin MA, Diaz J, Paradas C. Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis. JOURNAL OF NEUROLOGY. 2022; 269(7). DOI:10.1007/s00415-021-10957-0. PMID:35286480. IF:6 (Q1/2D). Document type: Article.
Fernandez E, Suarez X, Carrasco A, Pinol P, Lopez S, Pons G, Serra JJB, de la Torre C, De Luna N, Gallardo E, Diaz J. RhoA/ROCK2 signalling is enhanced by PDGF-AA in fibro-adipogenic progenitor cells: implications for Duchenne muscular dystrophy. Journal of Cachexia Sarcopenia and Muscle. 2022; 13(2). DOI:10.1002/jcsm.12923. PMID:35132805. IF:8,9 (Q1/1D). Document type: Article.
Garibaldi M, Nicoletti T, Bucci E, Fionda L, Leonardi L, Morino S, Tufano L, Alfieri G, Lauletta A, Merlonghi G, Perna A, Rossi S, Ricci E, Perez JA, Tartaglione T, Petrucci A, Pennisi EM, Salvetti M, Cutter G, Diaz J, Silvestri G, Antonini G. Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials. EUROPEAN JOURNAL OF NEUROLOGY. 2022; 29(3). DOI:10.1111/ene.15174. PMID:34753219. IF:5,1 (Q1/2D). Document type: Article.
Ingelfinger F, Sparano C, Bamert D, Reyes D, Sethi A, Rindlisbacher L, Zwicky P, Kreutmair S, Widmer CC, Mundt S, Cortés E, Tugues S, Becher B, Schreiner B. Azathioprine therapy induces selective NK cell depletion and IFN-? deficiency predisposing to herpesvirus reactivation. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 2022; 151(1). DOI:10.1016/j.jaci.2022.09.010. PMID:36122787. IF:9,4 (Q1/1D). Document type: Article.
Jentzer A, Attal A, Roue C, Raymond J, Lleixa C, Illa I, Querol L, Taieb G, Devaux J, Anti GRP. IgG4 Valency Modulates the Pathogenicity of Anti-Neurofascin-155 IgG4 in Autoimmune Nodopathy. Neurology-Neuroimmunology & Neuroinflammation. 2022; 9(5):e200014. DOI:10.1212/NXI.0000000000200014. PMID:35948442. IF:8,8 (Q1/1D). Document type: Article.
Koehorst E, Odria R, Capo J, Nunez J, Arbex A, Almendrote M, Linares I, Natera D, Saez V, Nascimento A, Ortez C, Rubio MA, Diaz J, Alonso J, Lucente G, Rodriguez A, Ramos A, Martinez A, Nogales G, Suelves M. An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic Dysregulation. Biomedicines. 2022; 10(6):1372. DOI:10.3390/biomedicines10061372. PMID:35740394. IF:4,7 (Q1/3D). Document type: Article.
Leonhard SE, van der Eijk AA, Andersen H, Antonini G, Arends S, Attarian S, Barroso FA, Bateman KJ, Batstra MR, Benedetti L, van den Berg B, Van den Bergh P, Burmann J, Busby M, Casasnovas C, Cornblath DR, Davidson A, Doets AY, van PA, de la Cour CD, Feasby TE, Fehmi J, Garcia T, Goldstein JM, Gorson KC, Granit V, Hadden RDM, Harbo T, Hartung HP, et al. [Martín-Aguilar L, Querol L]. An International Perspective on Preceding Infections in Guillain-Barre Syndrome The IGOS-1000 Cohort. NEUROLOGY. 2022; 99(12). DOI:10.1212/WNL.0000000000200885. PMID:35981895. IF:9,9 (Q1/1D). Document type: Article.
Liberatore G, De Lorenzo A, Giannotta C, Manganelli F, Filosto M, Cosentino G, Cocito D, Briani C, Cortese A, Fazio R, Lauria G, Clerici AM, Rosso T, Marfia GA, Antonini G, Cavaletti G, Carpo M, Doneddu PE, Spina E, Piccinelli SC, Peci E, Querol L, Nobile E. Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database. NEUROLOGICAL SCIENCES. 2022; 43(6). DOI:10.1007/s10072-021-05811-0. PMID:35048233. IF:3,3 (Q2/5D). Document type: Article.
Lokken N, Revsbech KL, Jacobsen LN, Martinuzzi A, Martin MA, Diaz J, Dominguez C, Brondani G, Musumeci O, Granata F, Stefan C, Merino C, Peralta CN, Khawajazada T, Alonso J, Toscano A, Vissing J. Muscle MRI in McArdle Disease A European Multicenter Observational Study. 2022; 99(15). DOI:10.1212/WNL.0000000000200914. PMID:35853747. IF:9,9 (Q1/1D). Document type: Article.
Martín L, Lleixà C, Pascual E, Caballero M, Martínez L, Díaz J, Rojas R, Cortés E, Turon J, de Luna N, Suárez X, Gallardo E, Rajabally Y, Scotton S, Jacobs BC, Baars A, Cortese A, Vegezzi E, Höftberger R, Zimprich F, Roesler C, Nobile E, Liberatore G, Hiew FL, Martínez A, Carvajal A, Piñar R, Usón M, Albertí O, López MÁ, Márquez F, Pardo J, Muñoz L, Cabrera M, Ortiz N, Bartolomé M, Duman Ö, Bril V, Segura D, Pitarokoili K, Steen C, Illa I, Querol L. Clinical and Laboratory Features in Anti-NF155 Autoimmune Nodopathy. Neurology-Neuroimmunology & Neuroinflammation. 2022; 9(1):e1098. DOI:10.1212/NXI.0000000000001098. PMID:34728497. IF:8,8 (Q1/1D). Document type: Article.
Martin L, Lleixa C, Pascual E. Autoimmune nodopathies, an emerging diagnostic category. CURRENT OPINION IN NEUROLOGY. 2022; 35(5). DOI:10.1097/WCO.0000000000001107. PMID:35989582. IF:4,8 (Q1/3D). Document type: Review.
Martín P, Fuenmayor CPD, Hernández A, Arteche A, Quesada JF, Voth AH, Vesperinas A, Olivé M, Domínguez C. Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene. MUSCLE & NERVE. 2022; 66(4). DOI:10.1002/mus.27678. PMID:35833674. IF:3,4 (Q2/5D). Document type: Letter.
Mayhew AG, James MK, Moore U, Sutherland H, Jacobs M, Feng J, Lowes LP, Alfano LN, Muni R, Rufibach LE, Rose K, Duong T, Bello L, Pedrosa I, Holsten S, Sakamoto C, Canal A, Sánchez N, Thiele S, Siener C, Vandevelde B, DeWolf B, Maron E, Gordish H, Hilsden H, Guglieri M, Hogrel J-Y, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Díaz J, Pegoraro E, Mendell JR, Straub V, Jain C. Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach. Frontiers in Neurology. 2022; 13:828525. DOI:10.3389/fneur.2022.828525. IF:3,4 (Q2/5D). Document type: Article.
Moore U, Araujo E, Reyngoudt H, Gordish H, Smith FE, Wilson I, James M, Mayhew A, Rufibach L, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Pegoraro E, Mendell JR, Bushby K, Blamire AM, Straub V, Carlier PG, Diaz J. Water T2 could predict functional decline in patients with dysferlinopathy. Journal of Cachexia Sarcopenia and Muscle. 2022; 13(6)DOI:10.1002/jcsm.13063. PMID:36058852. IF:8,9 (Q1/1D). Document type: Article.
Moore U, Fernandez R, Jacobs M, Gordish H, Diaz J, James MK, Mayhew AG, Harris E, Guglieri M, Rufibach LE, Feng J, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Pegoraro E, Lowes LP, Mendell JR, Bushby K, Bourke J, Straub V, Jain C. Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal study. MUSCLE & NERVE. 2022; 65(5). DOI:10.1002/mus.27524. PMID:35179231. IF:3,4 (Q2/5D). Document type: Article.
Poyatos J, Marti P, Liquori A, Muelas N, Pitarch I, Martinez L, Rodriguez B, Gonzalez L, Damia M, Aller E, Selva M, Vilchez R, Diaz J, Alonso J, Barcena JE, Jauregui A, Gamez J, Aladren JA, Fernandez A, Montolio M, Azorin I, Hervas D, Casasus A, Nieto M, Gallano P, Sevilla T, Vilchez JJ. Dystrophinopathy Phenotypes and Modifying Factors in DMD Exon 45-55 Deletion. ANNALS OF NEUROLOGY. 2022; 92(5). DOI:10.1002/ana.26461. PMID:35897138. IF:11,2 (Q1/1D). Document type: Article.
Querol LA, Hartung H-P, Lewis RA, van PA, Hammond TR, Atassi N, Alonso M, Dalakas MC. The Role of the Complement System in Chronic Inflammatory Demyelinating Polyneuropathy: Implications for Complement-Targeted Therapies. 2022; 19(3). DOI:10.1007/s13311-022-01221-y. PMID:35378684. IF:5,7 (Q1/2D). Document type: Review.
Ranta J, Olive M, Vandroux M, Roticiani G, Dominguez C, Johari M, Torella A, Bohm J, Turon J, Nigro V, Hackman P, Laporte J, Udd B, Savarese M. Mutation update for the ACTN2 gene. HUMAN MUTATION. 2022; 43(12)DOI:10.1002/humu.24470. PMID:36116040. IF:3,9 (Q2/3D). Document type: Article.
Reyes D, Aldecoa I, Gelpi E, Rojas R. Motor neuron involvement expands the neuropathological phenotype of late-onset ataxia in RFC1 mutation (CANVAS). BRAIN PATHOLOGY. 2022; 32(4):e13051. DOI:10.1111/bpa.13051. PMID:35001451. IF:6,4 (Q1/2D). Document type: Letter.
Reyes D, Dols O, Sirisi S, Cortes E, Turon J, De Luna N, Blesa R, Belbin O, Montal V, Alcolea D, Fortea J, Lleo A, Rojas R, Illan I. Pathophysiological Underpinnings of Extra-Motor Neurodegeneration in Amyotrophic Lateral Sclerosis: New Insights From Biomarker Studies. Frontiers in Neurology. 2022; 12:750543. DOI:10.3389/fneur.2021.750543. PMID:35115992. IF:3,4 (Q2/5D). Document type: Review.
Reyes D, Lopez J, Moga E, Pla F, Lynton E, Rojas R, Turon J, Querol L, Olive M, Alvarez R, Caballero M, Carbayo A, Vesperinas A, Domingo P, Illa I, Gallardo E, Cortes E. Immune Response and Safety of SARS-CoV-2 mRNA-1273 Vaccine in Patients With Myasthenia Gravis. Neurology-Neuroimmunology & Neuroinflammation. 2022; 9(4):e200002. DOI:10.1212/NXI.0000000000200002. PMID:35728947. IF:8,8 (Q1/1D). Document type: Article.
Reyngoudt H, Smith FE, Araujo E, Wilson I, Fernandez R, James MK, Moore UR, Diaz J, Marty B, Azzabou N, Gordish H, Rufibach L, Hodgson T, Wallace D, Ward L, Boisserie JM, Le J, Hilsden H, Sutherland H, Canal A, Hogrel JY, Jacobs M, Stojkovic T, Bushby K, Mayhew A, Straub V, Carlier PG, Blamire AM, Jain Clinical Outcome Study D. Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy. Journal of Cachexia Sarcopenia and Muscle. 2022; 13(3). DOI:10.1002/jcsm.12987. PMID:35373496. IF:8,9 (Q1/1D). Document type: Article.
Schiava M, Ikenaga C, Villar RN, Caballero M, Topf A, Nishino I, Kimonis V, Udd B, Schoser B, Zanoteli E, Souza PVS, Tasca G, Lloyd T, Lopez A, Paradas C, Pegoraro E, Nadaj A, De Bleecker J, Badrising U, Alonso A, Kostera A, Miralles F, Shin JH, Bevilacqua JA, Olive M, Vorgerd M, Kley R, Brady S, Williams T, Dominguez C, Papadimas GK, Warman J, Claeys KG, de Visser M, Muelas N, LaForet P, Malfatti E, Alfano LN, Nair SS, Manousakis G, Kushlaf HA, Harms MB, Nance C, Ramos A, Rodolico C, Hewamadduma C, Cetin H, Garcia J, Pal E, Farrugia ME, Lamont PJ, Quinn C, Nedkova V, Peric S, Luo SS, Oldfors A, Taylor K, Ralston S, Stojkovic T, Weihl C, Diaz J. Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 2022; 93(10). DOI:10.1136/jnnp-2022-328921. PMID:35896379. IF:11 (Q1/1D). Document type: Article.
Silva A, Rodrigo P, Moreno C, Mendonca RD, Estephan ED, Camelo CG, Campos ED, Dias AT, Nascimento AM, Kulikowski LD, Oliveira A, Reed UC, Goldfarb LG, Olive M, Zanoteli E. The Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic Aggregates. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 2022; 81(9)DOI:10.1093/jnen/nlac063. PMID:35898174. IF:3,2 (Q2/5D). Document type: Article.
Statland JM, Campbell C, Desai U, Karam C, Diaz J, Guptill JT, Korngut L, Genge A, Tawil RN, Elman L, Joyce NC, Wagner KR, Manousakis G, Amato AA, Butterfield RJ, Shieh PB, Wicklund M, Gamez J, Bodkin C, Pestronk A, Weihl CC, Vilchez JJ, Johnson NE, Mathews KD, Miller B, Leneus A, Fowler M, van de Rijn M, Attie KM. Randomized phase 2 study of ACE-083, a muscle-promoting agent, in facioscapulohumeral muscular dystrophy. MUSCLE & NERVE. 2022; 66(1). DOI:10.1002/mus.27558. PMID:35428982. IF:3,4 (Q2/5D). Document type: Article.

Publicaciones 2021

Allen JA, Eftimov F, Querol L. Outcome measures and biomarkers in chronic inflammatory demyelinating polyradiculoneuropathy: from research to clinical practice. Expert Review of Neurotherapeutics. 2021; 21(7). DOI:10.1080/14737175.2021.1944104. PMID:34130574. IF: 4,287
Alonso A, Fernandez E, Benito DND, Ortez C, Garcia C, Montiel E, Belmonte I, Pedrosa I, Segovia S, Pinol P, Carrasco A, Suarez X, Jimenez C, Nascimento A, Llauger J, Nunez C, Montesinos P, Alonso J, Gallardo E, Illa I, Diaz J. Platelet Derived Growth Factor-AA Correlates With Muscle Function Tests and Quantitative Muscle Magnetic Resonance in Dystrophinopathies. Frontiers in Neurology. 2021; 12:659922. DOI:10.3389/fneur.2021.659922. PMID:34177765. IF: 4,086
Alonso A, Nunez C, Montesinos P, Alonso J, Garcia C, Montiel E, Belmonte I, Pedrosa I, Segovia S, Llauger J, Diaz J. Different Approaches to Analyze Muscle Fat Replacement With Dixon MRI in Pompe Disease. Frontiers in Neurology. 2021; 12:675781. DOI:10.3389/fneur.2021.675781. PMID:34305788. IF: 4,086
Alonso J, Casasus A, Gimenez A, Duff J, Rojas R, Illa I, Straub V, Topf A, Diaz J. Late onset Sandhoff disease presenting with lower motor neuron disease and stuttering. NEUROMUSCULAR DISORDERS. 2021; 31(8). DOI:10.1016/j.nmd.2021.04.011. PMID:34210542. IF: 3,538
Alvarez R, Gutierrez G, Trujillo JC, Martinez E, Segovia S, Arribas M, Fernandez G, Paradas C, Velez B, Casasnovas C, Nedkova V, Guerrero A, Ramos A, Martinez A, Pardo J, Sevilla T, Gomez MT, de Munain AL, Jerico I, Pelayo AL, Martin MA, Morgado Y, Mendoza MD, Perez H, Rojas R, Turon J, Querol L, Gallardo E, Illa I, Cortes E. Clinical characteristics and outcomes of thymoma-associated myasthenia gravis. EUROPEAN JOURNAL OF NEUROLOGY. 2021; 28(6). DOI:10.1111/ene.14820. PMID:33721382. IF: 6,288
Borrego S, Turon J, Ximelis T, Aldecoa I, Molina L, Povedano M, Rubio MA, Gamez J, Cano A, Pare M, L, Sotoca J, Clarimon J, Balasa M, Antonell A, Llado A, Sanchez R, Rojas R, Gelpi E. Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants. BRAIN PATHOLOGY. 2021; 31(3):e12942. DOI:10.1111/bpa.12942. PMID:33576076. IF: 7,611
Conde E, Reyes D, Pintor L, Donaire A, Manzanares I, Rumia J, Roldan P, Boget T, Bargallo N, Gil FJ, Khawaja M, Setoain X, Centeno M, Carreno M. Psychotic symptoms in drug resistant epilepsy patients after cortical stimulation. EPILEPSY RESEARCH. 2021; 173:106630. DOI:10.1016/j.eplepsyres.2021.106630. PMID:33865048. IF: 2,991
Diaz J, Kishnani PS, Kushlaf H, Ladha S, Mozaffar T, Straub V, Toscano A, Van der Ploeg AT, Berger KI, Clemens PR, Chien YH, Day JW, Illarioshkin S, Roberts M, Attarian S, Borges JL, Bouhour F, Choi YC, Erdem S, Goker O, Kostera A, Haack KA, Hug C, Huynh O, Johnson J, Thibault N, Zhou TY, Dimachkie MM, Schoser B. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial. LANCET NEUROLOGY. 2021; 20(12). PMID:34800399. IF: 59,935
Diaz J, Walter G, Straub V. Skeletal muscle magnetic resonance imaging in Pompe disease. MUSCLE & NERVE. 2021; 63(5). DOI:10.1002/mus.27099. PMID:33155691. IF: 3,852
Diaz J. Fifteen years of enzyme therapy in Pompe disease. REVISTA DE NEUROLOGIA. 2021; 73(9). DOI:10.33588/rn.7309.2021382. PMID:34676531. IF: 1,235
Dominguez C, Madruga M, Hirano M, Marti I, Martin MA, Munell F, Nascimento A, Olive M, Quan J, Sardina MD, Marti R, Paradas C. Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency. Orphanet Journal of Rare Diseases. 2021; 16(1):407. DOI:10.1186/s13023-021-02030-w. PMID:34600563. IF: 4,303
Fionda L, Turon J, Prior PF, Noguera SB, Cortes E, Lopez MA, Gallardo E, Rojas R. A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?. JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 2021; 26(1). DOI:10.1111/jns.12425. PMID:33320396. IF: 5,188
Frasquet M, Rojas R, Argente H, Vazquez JF, Muelas N, Vilchez JJ, Sivera R, Millet E, Barreiro M, Diaz J, Turon J, Cortes E, Querol L, Ramirez L, Martinez D, Sanchez A, Espinos C, Sevilla T, Lupo V. Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation. EUROPEAN JOURNAL OF NEUROLOGY. 2021; 28(4). DOI:10.1111/ene.14700. PMID:33369814. IF: 6,288
Gelber PE, Ramirez E, Grau A, Gonzalez A, Llauger J, Farinas O. A new computed tomography scoring system to assess osteochondral allograft transplantation for the knee: inter-observer and intra-observer agreement. INTERNATIONAL ORTHOPAEDICS. 2021; 45(5). DOI:10.1007/s00264-020-04927-w. PMID:33416905. IF: 3,479
Gutschmidt K, Musumeci O, Diaz J, Chien YH, Knop KC, Wenninger S, Montagnese F, Pugliese A, Tavilla G, Alonso J, Hwu PWL, Toscano A, Schoser B. STIG study: real-world data of long-term outcomes of adults with Pompe disease under enzyme replacement therapy with alglucosidase alfa. JOURNAL OF NEUROLOGY. 2021; 268(7). DOI:10.1007/s00415-021-10409-9. PMID:33543425. IF: 6,682
Jacobs MB, James MK, Lowes LP, Alfano LN, Eagle M, Lofra RM, Moore U, Feng J, Rufibach LE, Rose K, Duong T, Bello L, Pedrosa I, Holsten S, Sakamoto C, Canal A, Praxedes N, Thiele S, Siener C, Vandevelde B, DeWolf B, Maron E, Guglieri M, Hogrel JY, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Et al. [Diaz J]. Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale. ANNALS OF NEUROLOGY. 2021; 89(5). DOI:10.1002/ana.26044. PMID:33576057. IF: 11,274
Lleixa C, Martin L, Pascual E, Franco T, Caballero M, De Luna N, Gallardo E, Suarez X, Martinez L, Diaz J, Rojas R, Cortes E, Turon J, Casasnovas C, Homedes C, Gutierrez G, Jimeno MC, Berciano J, Sedano MJ, Garcia T, Pardo J, Marquez C, Rojas I, Jerico I, Martinez E, de la Tassa GM, Dominguez C, Juarez C, Illa I, Querol L. Autoantibody screening in Guillain-Barre syndrome. Journal of Neuroinflammation. 2021; 18(1):251. DOI:10.1186/s12974-021-02301-0. PMID:34719386. IF: 9,587
Luijten LWG, Leonhard SE, van der Eijk AA, Doets AY, Appeltshauser L, Arends S, Attarian S, Benedetti L, Briani C, Casasnovas C, Castellani F, Dardiotis E, Echaniz A, Garssen MPJ, Harbo T, Huizinga R, Humm AM, Jellema K, van der Kooi AJ, Kuitwaard K, Kuntzer T, Kusunoki S, Lascano AM, Martinez E, Rinaldi S, Samijn J, Scheidegger O, Tsouni P, Vicino A, Visser LH, Walgaard C, Wang YZ, Wirtz PW, Ripellino P, Jacobs BC, Martín L, Živkovic SA. Guillain-Barre syndrome after SARS-CoV-2 infection in an international prospective cohort study. BRAIN. 2021; 144(11). DOI:10.1093/brain/awab279. PMID:34553216. IF: 15,255
Mantegazza R, Wolfe GI, Muppidi S, Wiendl H, Fujita KP, O’Brien FL, Booth H, Howard JF, Illa I, Cortés E, Díaz J, Querol LA, Rojas R, Vidal N, RSG. Post-intervention Status in Patients With Refractory Myasthenia Gravis Treated With Eculizumab During REGAIN and Its Open-Label Extension. 2021; 96(4). DOI:10.1212/WNL.0000000000011207. PMID:33229455. IF: 11.800
Martel L, Alonso A, Bascunana H, Diaz J, Llauger J, Nunez C, Montesinos P, Webb SM, Valassi E. Prevalence of sarcopenia after remission of hypercortisolism and its impact on HRQoL. CLINICAL ENDOCRINOLOGY. 2021; 95(5). DOI:10.1111/cen.14568. PMID:34323296. IF: 3,523
Martel L, Alonso J, Bascunana H, Diaz J, Llauger J, Nunez C, Montesinos P, Webb SM, Valassi E. Intramuscular fatty infiltration and physical function in controlled acromegaly. EUROPEAN JOURNAL OF ENDOCRINOLOGY. 2021; 185(1). DOI:10.1530/EJE-21-0209. PMID:33950861. IF: 6,558
Martin L, Camps P, Lleixa C, Pascual E, Diaz J, Rojas R, De Luna N, Gallardo E, Cortes E, Munoz L, Alcolea D, Lleo A, Casasnovas C, Homedes C, Gutierrez G, Jimeno MC, Berciano J, Sedano MJ, Garcia T, Pardo J, Marquez C, Rojas I, Jerico I, Martinez E, de la Tassa GM, Dominguez C, Illa I, Querol L. Serum neurofilament light chain predicts long-term prognosis in Guillain-Barre syndrome patients. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 2021; 92(1). DOI:10.1136/jnnp-2020-323899. PMID:33154183. IF: 13,654
Meca JE, Maurino J, Perez F, Forero L, Sepulveda M, Calles C, Martinez ML, Gonzalez I, Boyero S, Romero L, Sempere AP, Meca V, Querol L, Costa L, Prefasi D, Gomez R, Ballesteros J. Quantifying the patient ‘ s perspective in neuromyelitis optica spectrum disorder: Psychometric properties of the SymptoMScreen questionnaire. PLoS One. 2021; 16(7):e0255317. DOI:10.1371/journal.pone.0255317. PMID:34324586. IF: 3,752
Meca JE, Prefasi D, Perez F, Forero L, Sepulveda M, Calles C, Martinez ML, Gonzalez I, Boyero S, Romero L, Sempere AP, Meca V, Querol L, Costa L, De Castro H, Canal N, Maurino J. Perception of Stigma in Patients with Neuromyelitis Optica Spectrum Disorder. Patient Preference and Adherence. 2021; 15. DOI:10.2147/PPA.S305707. PMID:33880015. IF: 2,314
Moore U, Gordish H, Diaz J, James MK, Mayhew AG, Guglieri M, Fernandez R, Rufibach LE, Feng J, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Pegoraro E, Lowes LP, Mendell JR, Bushby K, Straub V, Jain C. Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease. NEUROMUSCULAR DISORDERS. 2021; 31(4). DOI:10.1016/j.nmd.2021.01.009. PMID:33610434. IF: 3,538
Narayanaswami P, Sanders DB, Wolfe G, Benatar M, Cea G, Evoli A, Gilhus NE, Illa I, Kuntz NL, Massey J, Melms A, Murai H, Nicolle M, Palace J, Richman D, Verschuuren J. International Consensus Guidance for Management of Myasthenia Gravis 2020 Update. 2021; 96(3). DOI:10.1212/WNL.0000000000011124. PMID:33144515. IF: 11,800
Natera D, Foley AR, Dominguez C, Ortez C, Jain M, Mebrahtu A, Donkervoort S, Hu Y, Fink M, Yun PM, Ogata T, Medina J, Vigo M, Meilleur KG, Leach ME, Dastgir J, Diaz J, Carrera L, Exposito J, Alarcon M, Cuadras D, Montiel E, Milisenda JC, Dominguez R, Olive M, Colomer J, Jou C, Jimenez C, Bonnemann CG, Nascimento A. Association of Initial Maximal Motor Ability With Long-term Functional Outcome in Patients With COL6-Related Dystrophies. NEUROLOGY. 2021; 96(10). DOI:10.1212/WNL.0000000000011499. PMID:33441455. IF: 11,800
Nunez C, Montesinos P, Alonso A, Alonso J, Reyes D, Sanchez J, Llauger J, Segovia S, Belmonte I, Pedrosa I, Martinez A, Matellini B, Walter G, Diaz J. Magnetization Transfer Ratio in Lower Limbs of Late Onset Pompe Patients Correlates With Intramuscular Fat Fraction and Muscle Function Tests. Frontiers in Neurology. 2021; 12:634766. DOI:10.3389/fneur.2021.634766. PMID:33796064. IF: 4,086
Pascual E, Fehmi J, Lleixa C, Martin L, Devaux J, Hoftberger R, Delmont E, Doppler K, Sommer C, Radunovic A, Carvajal A, Smyth S, Williams L, Mazanec R, Potockova V, Hinds N, Cassereau J, Viala K, Lefilliatre M, Nicolas G, Foley P, Leypoldt F, Keddie S, Lunn MP, Zimprich F, Nunkoo VS, Loscher WN, Martinez L, Diaz J, Rojas R, Illa I, Rinaldi S, Querol L. Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathy. BRAIN. 2021; 144. PMID:33880507. IF: 15,255
Querol L, Crabtree M, Herepath M, Priedane E, Viejo IV, Agush S, Sommerer P. Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP). JOURNAL OF NEUROLOGY. 2021; 268(10). DOI:10.1007/s00415-020-09998-8. PMID:32583051. IF: 6,682
Querol L, Lleixa C. Novel Immunological and Therapeutic Insights in Guillain-Barre Syndrome and CIDP. Neurotherapeutics. 2021; 18(4). DOI:10.1007/s13311-021-01117-3. PMID:34549385. IF: 6,088
Reyes D, Alonso J, Mayos M, Nunez C, Llauger J, Belmonte I, Pedrosa I, Segovia S, Diaz J. Correlation Between Respiratory Accessory Muscles and Diaphragm Pillars MRI and Pulmonary Function Test in Late-Onset Pompe Disease Patients. Frontiers in Neurology. 2021; 12:621257. DOI:10.3389/fneur.2021.621257. PMID:33732206. IF: 4,086
Ripellino P, Ventura E, Querol L, Gobbi C. Chronic inflammatory demyelinating polyneuropathy with hypertrophic nerves. JOURNAL OF THE PERIPHERAL NERVOUS 2021; 26(2). DOI:10.1111/jns.12445. PMID:33881184. IF: 5,188
Schoser B, Roberts M, Byrne BJ, Sitaraman S, Jiang H, Laforêt P, Toscano A, Castelli J, Díaz J, Goldman M, van der Ploeg AT, Bratkovic D, Kuchipudi S, Mozaffar T, Kishnani PS, Sebok A, Pestronk A, Dominovic A, Khan A, Koritnik B, Tard C, Lindberg C, Quinn C, Eldridge C, Bodkin C, Reyes D, Hughes D, Stefanescu E, Salort E, Butler E, et al. [Alonso J, Vidal N]. Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double-blind, parallel-group, phase 3 trial. LANCET NEUROLOGY. 2021; 20(12). DOI:10.1016/S1474-4422(21)00331-8. PMID:34800400. IF: 59,935
Siddiqi ZA, Nowak RJ, Mozaffar T, O’Brien F, Yountz M, Patti F, Illa I, Cortés E, Díaz J, Querol LA, Rojas R, Vidal N, Nye JL. Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab: subgroup analysis of REGAIN and its extension study. MUSCLE & NERVE. 2021; 64(6). DOI:10.1002/mus.27422. PMID:34590717. IF: 3,852
Sivera R, Lupo V, Frasquet M, Argente H, Alonso J, Diaz J, Querol L, Garcia MD, Pascual SI, Garcia T, Paradas C, Vazquez JF, Muelas N, Millet E, Vilchez JJ, Espinos C, Sevilla T. Charcot-Marie-Tooth disease due to MORC2 mutations in Spain. EUROPEAN JOURNAL OF NEUROLOGY. 2021; 28(9). DOI:10.1111/ene.15001. PMID:34189813. IF: 6,288
Suarez X, Fernandez E, Pinol P, Alonso J, Carrasco A, Lleixa C, Lopez S, Pons G, Soria L, Bigot A, Mouly V, Illa I, Gallardo E, Jaiswal JK, Diaz J. Isolation of human fibroadipogenic progenitors and satellite cells from frozen muscle biopsies. FASEB JOURNAL. 2021; 35(9):e21819. DOI:10.1096/fj.202100588R. PMID:34405910. IF: 5,834
Van den Bergh PYK, van PA, Hadden RDM, Avau B, Vankrunkelsven P, Allen JA, Attarian S, Blomkwist PH, Cornblath DR, Eftimov F, Goedee HS, Harbo T, Kuwabara S, Lewis RA, Lunn MP, Nobile E, Querol L, Rajabally YA, Sommer C, Topaloglu HA. European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force-Second revision. JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 2021; 26(3). DOI:10.1111/jns.12455. PMID:34085743. IF: 5,188
Van Rheenen W, van der Spek R, Bakker MK, van J, Hop PJ, Zwamborn R, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker AM, Gawor K, Westeneng HJ, Tazelaar GHP, van KR, Kooyman M, Byrne RP, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, et al. [Rojas R]. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. NATURE GENETICS. 2021; 53(12). DOI:10.1038/s41588-021-00973-1. PMID:34873335. IF: 41,307
Verboon C, Harbo T, Cornblath DR, Hughes R, van PA, Lunn MP, Gorson KC, Barroso F, Kuwabara S, Galassi G, Lehmann HC, Kusunoki S, Reisin RC, Binda D, Cavaletti G, Jacobs BC, Querol LA, Wirtz PW. Intravenous immunoglobulin treatment for mild Guillain-Barre syndrome: an international observational study. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 2021; 92(10). DOI:10.1136/jnnp-2020-325815. PMID:34103340. IF: 13,654
Wieske L, Martin L, Fehmi J, Lleixa C, Koel M, Chatterjee M, van Z, Killestein J, Verhamme C, Querol L, Rinaldi S, Teunissen CE, Eftimov F. Serum Contactin-1 in CIDP A Cross-Sectional Study. Neurology-Neuroimmunology & Neuroinflammation. 2021; 8(5):e1040. DOI:10.1212/NXI.0000000000001040. PMID:34285092. IF: 11,360

2017 Scientific Report – Neuromuscular Diseases

Presentación

Principales líneas de investigación

Enfermedades neuromusculares inmunomediadas

Caracterización de nuevos antígenos diana en Myasthenia Gravis y neuropatías inmunomediadas (CIDP, GBS, NMM). Utilización como biomarcadores diagnósticos y terapéuticos.
Patogénesis de nuevos antígenos paranodales en CIDP.
Análisis de la inmunidad innata en miopatías inflamatorias.
Anáisis del impacto de nuevas terapias modulares en enfermedades neuromusculares mediadas por IgG4.
Aspectos funcionales de las células del sistema inmunitario (respuesta a ligandos, producción de anticuerpos, etc.).
Base de datos IGOS para el síndrome de Guillain Barré.
Registro español NMD-ES para enfermedades neuromusculares.

Distrofia muscular, disferlinopatía y miopatías distales

Análisis de MRI muscular como biomarcador para varias distrofias musculares.
Estudio de los perfiles de miRNA y secretoma muscular en distrofias musculares.
Estudio del rol de PDGF en fibrosis de distrofias musculares.
Historia natural de las disferlinopatías. Estudio de resultados clínicos de la Jain Foundation.
Evaluación de la frecuencia de portadores de mutaciones en el gen diferlina en la población normal.

Esclerosis lateral amiotrófica

Epidemiología de ELA en Cataluña.
Perfil genético de pacientes de ELA en España.
Perfil de biomarcadores en diferentes fenotipos de ELA.

Retos

Incrementar el conocimiento de los mecanismos inmunológicos involucrados en la patogénesis de enfermedades neuromusculares autoinmunitarias (MG, CIDP, NMM).
Incrementar el conocimiento de los mecanismos patogénicos en miopatías inflamatorias (DM, PM, IBM).
Buscar nuevos antígenos y desarrollar tests diagnósticos con nuevos biomarcadores en neuropatías mediadas por el sistema inmunitario y Myasthenia Gravis.
Implementar nuevos métodos diagnósticos y de seguimiento de la enfermedad por distrofias musculares resultantes de la disferlinopatía y otras miopatías (biomarcadores – miRNA, secretoma-. MRI, etc.).
Incrementar el conocimiento de los mecanismos patogénicos involucrados en la distrofia muscular resultante de la deficiencia en disferlina y otras distrofias musculares.
Acceso a la sala limpia para manipular células para su uso en humanos.
Utilización del registro NMD.ES para desarrollar investigación en varias enfermedades neuromusculares.

Información adicional : Neuromuscularbcn

Equipo

Coordinación del grupo

OLIVE PLANA, MONTSERRAT FGS
molive@santpau.cat

Miembros

Producción científica

Publicaciones 2022

(JIF 2022)

Alonso J, Carrasco A, Borrell M, Fernandez E, Pinol P, Badimon L, Wollin L, Lleixa C, Gallardo E, Olive M, Diaz J, Suarez X. Nintedanib Reduces Muscle Fibrosis and Improves Muscle Function of the Alpha-Sarcoglycan-Deficient Mice. Biomedicines. 2022; 10(10):2629. DOI:10.3390/biomedicines10102629. PMID:36289891. IF:4,7 (Q1/3D). Document type: Article.
Alonso J, Gonzalez L, Bruno C, Panicucci C, Alavi A, Nafissi S, Nilipour Y, Zanoteli E, Isihi LMD, Melegh B, Hadzsiev K, Muelas N, Vilchez JJ, Dourado ME, Kadem N, Kutluk G, Umair M, Younus M, Pegorano E, Bello L, Crawford TO, Suarez X, Topf A, Guglieri M, Marini C, Gallano P, Straub V, Diaz J. Clinical and genetic spectrum of a large cohort of patients with delta-sarcoglycan muscular dystrophy. 2022; 145(2). DOI:10.1093/brain/awab301. PMID:34515763. IF:14,5 (Q1/1D). Document type: Article.
Alonso J, Hernandez JCD, Perez H, Mendoza MD, Gutierrez AJ, Hadjigeorgiou I, Monton F, Gonzalez L, Alonso A, Suarez X, Diaz J. Clinical and genetic features of a large homogeneous cohort of oculopharyngeal muscular dystrophy patients from the Canary Islands. EUROPEAN JOURNAL OF NEUROLOGY. 2022; 29(5). DOI:10.1111/ene.15252. PMID:35112761. IF:5,1 (Q1/2D). Document type: Article.
Alvarez R, Nunez CA, Alonso J, Gallardo E, Collet R, Reyes D, Pascual E, Martin L, Caballero M, Carbayo A, Llauger J, Diaz J, Olive M. High prevalence of paraspinal muscle involvement in adults with McArdle disease. MUSCLE & NERVE. 2022; 65(5). DOI:10.1002/mus.27523. PMID:35174518. IF:3,4 (Q2/5D). Document type: Article.
Blasco L, Costa M, Leno J, Bernal S, Alias L, Codina M, Martinez D, Castiglioni C, Bertini E, Travaglini L, Millan JM, Aller E, Sotoca J, Juntas R, Hoei CE, Moreno A, Guillen E, Costa L, Munell F, Boronat S, Rojas R, Povedano M, Cusco I, Tizzano EF. Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G > C Variant in SMN2. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2022; 23(15):8289. DOI:10.3390/ijms23158289. PMID:35955418. IF:5,6 (Q1/3D). Document type: Article.
Bolano C, Diaz J. Therapeutic Options for the Management of Pompe Disease: Current Challenges and Clinical Evidence in Therapeutics and Clinical Risk Management. Therapeutics and Clinical Risk Management. 2022; 18. DOI:10.2147/TCRM.S334232. PMID:36536827. IF:2,8 (Q3/6D). Document type: Review.
Bullich G, Matalonga L, Pujadas M, Papakonstantinou A, Piscia D, Tonda R, Artuch R, Gallano P, Garrabou G, González JR, Grinberg D, Guitart M, Laurie S, Lázaro C, Luengo C, Martí R, Milà M, Ovelleiro D, Parra G, Pujol A, Tizzano E, Macaya A, Palau F, Ribes A, Pérez LA, Beltran S, Schlüter A, Rodriguez A, Cáceres A, Nascimento A, García À, Cueto A, Marcé A, NELLOAR, Martínez A, et al. [Díaz-Manera J, Rojas-García R, Bernal S, Boronat S]. Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases. JOURNAL OF MOLECULAR DIAGNOSTICS. 2022; 24(5). DOI:10.1016/j.jmoldx.2022.02.003. PMID:35569879. IF:4,1 (Q2/3D). Document type: Article.
Caballero M, Álvarez R, Moga E, Rojas R, Turon J, Querol L, Olivé M, Reyes D, Illa I, Gallardo E, Cortés E. Rituximab in myasthenia gravis: efficacy, associated infections and risk of induced hypogammaglobulinemia. NEUROMUSCULAR DISORDERS. 2022; 32(8). DOI:10.1016/j.nmd.2022.06.006. PMID:35811274. IF:2,8 (Q3/6D). Document type: Article.
Carrasco A, Fernandez E, Suarez X, Pinol P, Alonso J, de Luna N, Schoser B, Meinke P, Dominguez C, Hernandez A, Paradas C, Rivas E, Illa I, Olive M, Gallardo E, Diaz J. BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients. AMERICAN JOURNAL OF PATHOLOGY. 2022; 192(8). DOI:10.1016/j.ajpath.2022.05.003. PMID:35605642. IF:6 (Q1/2D). Document type: Article.
Cortes E, Alvarez R, Pla F, Rojas R, Paradas C, Sevilla T, Casasnovas C, Gomez MT, Pardo J, Ramos A, Pelayo AL, Gutierrez G, Turon J, de Munain AL, Guerrero A, Jerico I, Martin MA, Mendoza MD, Moris G, Velez B, Garcia T, Pascual E, Reyes D, Illa I, Gallardo E. Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome. Annals of Clinical and Translational Neurology. 2022; 9(2). DOI:10.1002/acn3.51492. PMID:35080153. IF:5,3 (Q1/2D). Document type: Article.
Doets AY, Lingsma HF, Walgaard C, Islam B, Papri N, Davidson A, Yamagishi Y, Kusunoki S, Dimachkie MM, Waheed W, Kolb N, Islam Z, Mohammad QD, Harbo T, Sindrup SH, Chavada G, Willison HJ, Casasnovas C, Bateman K, Miller JAL, van den Berg B, Verboon C, Roodbol J, Leonhard SE, Benedetti L, Kuwabara S, van den Bergh P, Monges S, Marfia GA, Shahrizaila N, et al. [Querol L]. Predicting Outcome in Guillain-Barré Syndrome International Validation of the Modified Erasmus GBS Outcome Score. 2022; 98(5). DOI:10.1212/WNL.0000000000013139. PMID:34937789. IF:9,9 (Q1/1D). Document type: Article.
Dominguez C, Diaz C, Juntas R, Nascimiento A, Rivera A, Diaz J. Survey on the management of Pompe disease in routine clinical practice in Spain. Orphanet Journal of Rare Diseases. 2022; 17(1):426. DOI:10.1186/s13023-022-02574-5. PMID:36471448. IF:3,7 (Q2/4D). Document type: Article.
Dominguez C, Fernandez R, Moore U, de la Hoz CPDF, Velez B, Cabezas JA, Alonso J, Gonzalez L, Olive M, Garcia J, Moris G, Hernandez JCL, Muelas N, Servian E, Martin MA, Diaz J, Paradas C. Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis. JOURNAL OF NEUROLOGY. 2022; 269(7). DOI:10.1007/s00415-021-10957-0. PMID:35286480. IF:6 (Q1/2D). Document type: Article.
Fernandez E, Suarez X, Carrasco A, Pinol P, Lopez S, Pons G, Serra JJB, de la Torre C, De Luna N, Gallardo E, Diaz J. RhoA/ROCK2 signalling is enhanced by PDGF-AA in fibro-adipogenic progenitor cells: implications for Duchenne muscular dystrophy. Journal of Cachexia Sarcopenia and Muscle. 2022; 13(2). DOI:10.1002/jcsm.12923. PMID:35132805. IF:8,9 (Q1/1D). Document type: Article.
Garibaldi M, Nicoletti T, Bucci E, Fionda L, Leonardi L, Morino S, Tufano L, Alfieri G, Lauletta A, Merlonghi G, Perna A, Rossi S, Ricci E, Perez JA, Tartaglione T, Petrucci A, Pennisi EM, Salvetti M, Cutter G, Diaz J, Silvestri G, Antonini G. Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials. EUROPEAN JOURNAL OF NEUROLOGY. 2022; 29(3). DOI:10.1111/ene.15174. PMID:34753219. IF:5,1 (Q1/2D). Document type: Article.
Ingelfinger F, Sparano C, Bamert D, Reyes D, Sethi A, Rindlisbacher L, Zwicky P, Kreutmair S, Widmer CC, Mundt S, Cortés E, Tugues S, Becher B, Schreiner B. Azathioprine therapy induces selective NK cell depletion and IFN-? deficiency predisposing to herpesvirus reactivation. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 2022; 151(1). DOI:10.1016/j.jaci.2022.09.010. PMID:36122787. IF:9,4 (Q1/1D). Document type: Article.
Jentzer A, Attal A, Roue C, Raymond J, Lleixa C, Illa I, Querol L, Taieb G, Devaux J, Anti GRP. IgG4 Valency Modulates the Pathogenicity of Anti-Neurofascin-155 IgG4 in Autoimmune Nodopathy. Neurology-Neuroimmunology & Neuroinflammation. 2022; 9(5):e200014. DOI:10.1212/NXI.0000000000200014. PMID:35948442. IF:8,8 (Q1/1D). Document type: Article.
Koehorst E, Odria R, Capo J, Nunez J, Arbex A, Almendrote M, Linares I, Natera D, Saez V, Nascimento A, Ortez C, Rubio MA, Diaz J, Alonso J, Lucente G, Rodriguez A, Ramos A, Martinez A, Nogales G, Suelves M. An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic Dysregulation. Biomedicines. 2022; 10(6):1372. DOI:10.3390/biomedicines10061372. PMID:35740394. IF:4,7 (Q1/3D). Document type: Article.
Leonhard SE, van der Eijk AA, Andersen H, Antonini G, Arends S, Attarian S, Barroso FA, Bateman KJ, Batstra MR, Benedetti L, van den Berg B, Van den Bergh P, Burmann J, Busby M, Casasnovas C, Cornblath DR, Davidson A, Doets AY, van PA, de la Cour CD, Feasby TE, Fehmi J, Garcia T, Goldstein JM, Gorson KC, Granit V, Hadden RDM, Harbo T, Hartung HP, et al. [Martín-Aguilar L, Querol L]. An International Perspective on Preceding Infections in Guillain-Barre Syndrome The IGOS-1000 Cohort. NEUROLOGY. 2022; 99(12). DOI:10.1212/WNL.0000000000200885. PMID:35981895. IF:9,9 (Q1/1D). Document type: Article.
Liberatore G, De Lorenzo A, Giannotta C, Manganelli F, Filosto M, Cosentino G, Cocito D, Briani C, Cortese A, Fazio R, Lauria G, Clerici AM, Rosso T, Marfia GA, Antonini G, Cavaletti G, Carpo M, Doneddu PE, Spina E, Piccinelli SC, Peci E, Querol L, Nobile E. Frequency and clinical correlates of anti-nerve antibodies in a large population of CIDP patients included in the Italian database. NEUROLOGICAL SCIENCES. 2022; 43(6). DOI:10.1007/s10072-021-05811-0. PMID:35048233. IF:3,3 (Q2/5D). Document type: Article.
Lokken N, Revsbech KL, Jacobsen LN, Martinuzzi A, Martin MA, Diaz J, Dominguez C, Brondani G, Musumeci O, Granata F, Stefan C, Merino C, Peralta CN, Khawajazada T, Alonso J, Toscano A, Vissing J. Muscle MRI in McArdle Disease A European Multicenter Observational Study. 2022; 99(15). DOI:10.1212/WNL.0000000000200914. PMID:35853747. IF:9,9 (Q1/1D). Document type: Article.
Martín L, Lleixà C, Pascual E, Caballero M, Martínez L, Díaz J, Rojas R, Cortés E, Turon J, de Luna N, Suárez X, Gallardo E, Rajabally Y, Scotton S, Jacobs BC, Baars A, Cortese A, Vegezzi E, Höftberger R, Zimprich F, Roesler C, Nobile E, Liberatore G, Hiew FL, Martínez A, Carvajal A, Piñar R, Usón M, Albertí O, López MÁ, Márquez F, Pardo J, Muñoz L, Cabrera M, Ortiz N, Bartolomé M, Duman Ö, Bril V, Segura D, Pitarokoili K, Steen C, Illa I, Querol L. Clinical and Laboratory Features in Anti-NF155 Autoimmune Nodopathy. Neurology-Neuroimmunology & Neuroinflammation. 2022; 9(1):e1098. DOI:10.1212/NXI.0000000000001098. PMID:34728497. IF:8,8 (Q1/1D). Document type: Article.
Martin L, Lleixa C, Pascual E. Autoimmune nodopathies, an emerging diagnostic category. CURRENT OPINION IN NEUROLOGY. 2022; 35(5). DOI:10.1097/WCO.0000000000001107. PMID:35989582. IF:4,8 (Q1/3D). Document type: Review.
Martín P, Fuenmayor CPD, Hernández A, Arteche A, Quesada JF, Voth AH, Vesperinas A, Olivé M, Domínguez C. Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene. MUSCLE & NERVE. 2022; 66(4). DOI:10.1002/mus.27678. PMID:35833674. IF:3,4 (Q2/5D). Document type: Letter.
Mayhew AG, James MK, Moore U, Sutherland H, Jacobs M, Feng J, Lowes LP, Alfano LN, Muni R, Rufibach LE, Rose K, Duong T, Bello L, Pedrosa I, Holsten S, Sakamoto C, Canal A, Sánchez N, Thiele S, Siener C, Vandevelde B, DeWolf B, Maron E, Gordish H, Hilsden H, Guglieri M, Hogrel J-Y, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Díaz J, Pegoraro E, Mendell JR, Straub V, Jain C. Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach. Frontiers in Neurology. 2022; 13:828525. DOI:10.3389/fneur.2022.828525. IF:3,4 (Q2/5D). Document type: Article.
Moore U, Araujo E, Reyngoudt H, Gordish H, Smith FE, Wilson I, James M, Mayhew A, Rufibach L, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Pegoraro E, Mendell JR, Bushby K, Blamire AM, Straub V, Carlier PG, Diaz J. Water T2 could predict functional decline in patients with dysferlinopathy. Journal of Cachexia Sarcopenia and Muscle. 2022; 13(6)DOI:10.1002/jcsm.13063. PMID:36058852. IF:8,9 (Q1/1D). Document type: Article.
Moore U, Fernandez R, Jacobs M, Gordish H, Diaz J, James MK, Mayhew AG, Harris E, Guglieri M, Rufibach LE, Feng J, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori M, Bravver E, Pegoraro E, Lowes LP, Mendell JR, Bushby K, Bourke J, Straub V, Jain C. Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal study. MUSCLE & NERVE. 2022; 65(5). DOI:10.1002/mus.27524. PMID:35179231. IF:3,4 (Q2/5D). Document type: Article.
Poyatos J, Marti P, Liquori A, Muelas N, Pitarch I, Martinez L, Rodriguez B, Gonzalez L, Damia M, Aller E, Selva M, Vilchez R, Diaz J, Alonso J, Barcena JE, Jauregui A, Gamez J, Aladren JA, Fernandez A, Montolio M, Azorin I, Hervas D, Casasus A, Nieto M, Gallano P, Sevilla T, Vilchez JJ. Dystrophinopathy Phenotypes and Modifying Factors in DMD Exon 45-55 Deletion. ANNALS OF NEUROLOGY. 2022; 92(5). DOI:10.1002/ana.26461. PMID:35897138. IF:11,2 (Q1/1D). Document type: Article.
Querol LA, Hartung H-P, Lewis RA, van PA, Hammond TR, Atassi N, Alonso M, Dalakas MC. The Role of the Complement System in Chronic Inflammatory Demyelinating Polyneuropathy: Implications for Complement-Targeted Therapies. 2022; 19(3). DOI:10.1007/s13311-022-01221-y. PMID:35378684. IF:5,7 (Q1/2D). Document type: Review.
Ranta J, Olive M, Vandroux M, Roticiani G, Dominguez C, Johari M, Torella A, Bohm J, Turon J, Nigro V, Hackman P, Laporte J, Udd B, Savarese M. Mutation update for the ACTN2 gene. HUMAN MUTATION. 2022; 43(12)DOI:10.1002/humu.24470. PMID:36116040. IF:3,9 (Q2/3D). Document type: Article.
Reyes D, Aldecoa I, Gelpi E, Rojas R. Motor neuron involvement expands the neuropathological phenotype of late-onset ataxia in RFC1 mutation (CANVAS). BRAIN PATHOLOGY. 2022; 32(4):e13051. DOI:10.1111/bpa.13051. PMID:35001451. IF:6,4 (Q1/2D). Document type: Letter.
Reyes D, Dols O, Sirisi S, Cortes E, Turon J, De Luna N, Blesa R, Belbin O, Montal V, Alcolea D, Fortea J, Lleo A, Rojas R, Illan I. Pathophysiological Underpinnings of Extra-Motor Neurodegeneration in Amyotrophic Lateral Sclerosis: New Insights From Biomarker Studies. Frontiers in Neurology. 2022; 12:750543. DOI:10.3389/fneur.2021.750543. PMID:35115992. IF:3,4 (Q2/5D). Document type: Review.
Reyes D, Lopez J, Moga E, Pla F, Lynton E, Rojas R, Turon J, Querol L, Olive M, Alvarez R, Caballero M, Carbayo A, Vesperinas A, Domingo P, Illa I, Gallardo E, Cortes E. Immune Response and Safety of SARS-CoV-2 mRNA-1273 Vaccine in Patients With Myasthenia Gravis. Neurology-Neuroimmunology & Neuroinflammation. 2022; 9(4):e200002. DOI:10.1212/NXI.0000000000200002. PMID:35728947. IF:8,8 (Q1/1D). Document type: Article.
Reyngoudt H, Smith FE, Araujo E, Wilson I, Fernandez R, James MK, Moore UR, Diaz J, Marty B, Azzabou N, Gordish H, Rufibach L, Hodgson T, Wallace D, Ward L, Boisserie JM, Le J, Hilsden H, Sutherland H, Canal A, Hogrel JY, Jacobs M, Stojkovic T, Bushby K, Mayhew A, Straub V, Carlier PG, Blamire AM, Jain Clinical Outcome Study D. Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy. Journal of Cachexia Sarcopenia and Muscle. 2022; 13(3). DOI:10.1002/jcsm.12987. PMID:35373496. IF:8,9 (Q1/1D). Document type: Article.
Schiava M, Ikenaga C, Villar RN, Caballero M, Topf A, Nishino I, Kimonis V, Udd B, Schoser B, Zanoteli E, Souza PVS, Tasca G, Lloyd T, Lopez A, Paradas C, Pegoraro E, Nadaj A, De Bleecker J, Badrising U, Alonso A, Kostera A, Miralles F, Shin JH, Bevilacqua JA, Olive M, Vorgerd M, Kley R, Brady S, Williams T, Dominguez C, Papadimas GK, Warman J, Claeys KG, de Visser M, Muelas N, LaForet P, Malfatti E, Alfano LN, Nair SS, Manousakis G, Kushlaf HA, Harms MB, Nance C, Ramos A, Rodolico C, Hewamadduma C, Cetin H, Garcia J, Pal E, Farrugia ME, Lamont PJ, Quinn C, Nedkova V, Peric S, Luo SS, Oldfors A, Taylor K, Ralston S, Stojkovic T, Weihl C, Diaz J. Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 2022; 93(10). DOI:10.1136/jnnp-2022-328921. PMID:35896379. IF:11 (Q1/1D). Document type: Article.
Silva A, Rodrigo P, Moreno C, Mendonca RD, Estephan ED, Camelo CG, Campos ED, Dias AT, Nascimento AM, Kulikowski LD, Oliveira A, Reed UC, Goldfarb LG, Olive M, Zanoteli E. The Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic Aggregates. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 2022; 81(9)DOI:10.1093/jnen/nlac063. PMID:35898174. IF:3,2 (Q2/5D). Document type: Article.
Statland JM, Campbell C, Desai U, Karam C, Diaz J, Guptill JT, Korngut L, Genge A, Tawil RN, Elman L, Joyce NC, Wagner KR, Manousakis G, Amato AA, Butterfield RJ, Shieh PB, Wicklund M, Gamez J, Bodkin C, Pestronk A, Weihl CC, Vilchez JJ, Johnson NE, Mathews KD, Miller B, Leneus A, Fowler M, van de Rijn M, Attie KM. Randomized phase 2 study of ACE-083, a muscle-promoting agent, in facioscapulohumeral muscular dystrophy. MUSCLE & NERVE. 2022; 66(1). DOI:10.1002/mus.27558. PMID:35428982. IF:3,4 (Q2/5D). Document type: Article.

Publicaciones 2021

Allen JA, Eftimov F, Querol L. Outcome measures and biomarkers in chronic inflammatory demyelinating polyradiculoneuropathy: from research to clinical practice. Expert Review of Neurotherapeutics. 2021; 21(7). DOI:10.1080/14737175.2021.1944104. PMID:34130574. IF: 4,287
Alonso A, Fernandez E, Benito DND, Ortez C, Garcia C, Montiel E, Belmonte I, Pedrosa I, Segovia S, Pinol P, Carrasco A, Suarez X, Jimenez C, Nascimento A, Llauger J, Nunez C, Montesinos P, Alonso J, Gallardo E, Illa I, Diaz J. Platelet Derived Growth Factor-AA Correlates With Muscle Function Tests and Quantitative Muscle Magnetic Resonance in Dystrophinopathies. Frontiers in Neurology. 2021; 12:659922. DOI:10.3389/fneur.2021.659922. PMID:34177765. IF: 4,086
Alonso A, Nunez C, Montesinos P, Alonso J, Garcia C, Montiel E, Belmonte I, Pedrosa I, Segovia S, Llauger J, Diaz J. Different Approaches to Analyze Muscle Fat Replacement With Dixon MRI in Pompe Disease. Frontiers in Neurology. 2021; 12:675781. DOI:10.3389/fneur.2021.675781. PMID:34305788. IF: 4,086
Alonso J, Casasus A, Gimenez A, Duff J, Rojas R, Illa I, Straub V, Topf A, Diaz J. Late onset Sandhoff disease presenting with lower motor neuron disease and stuttering. NEUROMUSCULAR DISORDERS. 2021; 31(8). DOI:10.1016/j.nmd.2021.04.011. PMID:34210542. IF: 3,538
Alvarez R, Gutierrez G, Trujillo JC, Martinez E, Segovia S, Arribas M, Fernandez G, Paradas C, Velez B, Casasnovas C, Nedkova V, Guerrero A, Ramos A, Martinez A, Pardo J, Sevilla T, Gomez MT, de Munain AL, Jerico I, Pelayo AL, Martin MA, Morgado Y, Mendoza MD, Perez H, Rojas R, Turon J, Querol L, Gallardo E, Illa I, Cortes E. Clinical characteristics and outcomes of thymoma-associated myasthenia gravis. EUROPEAN JOURNAL OF NEUROLOGY. 2021; 28(6). DOI:10.1111/ene.14820. PMID:33721382. IF: 6,288
Borrego S, Turon J, Ximelis T, Aldecoa I, Molina L, Povedano M, Rubio MA, Gamez J, Cano A, Pare M, L, Sotoca J, Clarimon J, Balasa M, Antonell A, Llado A, Sanchez R, Rojas R, Gelpi E. Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants. BRAIN PATHOLOGY. 2021; 31(3):e12942. DOI:10.1111/bpa.12942. PMID:33576076. IF: 7,611
Conde E, Reyes D, Pintor L, Donaire A, Manzanares I, Rumia J, Roldan P, Boget T, Bargallo N, Gil FJ, Khawaja M, Setoain X, Centeno M, Carreno M. Psychotic symptoms in drug resistant epilepsy patients after cortical stimulation. EPILEPSY RESEARCH. 2021; 173:106630. DOI:10.1016/j.eplepsyres.2021.106630. PMID:33865048. IF: 2,991
Diaz J, Kishnani PS, Kushlaf H, Ladha S, Mozaffar T, Straub V, Toscano A, Van der Ploeg AT, Berger KI, Clemens PR, Chien YH, Day JW, Illarioshkin S, Roberts M, Attarian S, Borges JL, Bouhour F, Choi YC, Erdem S, Goker O, Kostera A, Haack KA, Hug C, Huynh O, Johnson J, Thibault N, Zhou TY, Dimachkie MM, Schoser B. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial. LANCET NEUROLOGY. 2021; 20(12). PMID:34800399. IF: 59,935
Diaz J, Walter G, Straub V. Skeletal muscle magnetic resonance imaging in Pompe disease. MUSCLE & NERVE. 2021; 63(5). DOI:10.1002/mus.27099. PMID:33155691. IF: 3,852
Diaz J. Fifteen years of enzyme therapy in Pompe disease. REVISTA DE NEUROLOGIA. 2021; 73(9). DOI:10.33588/rn.7309.2021382. PMID:34676531. IF: 1,235
Dominguez C, Madruga M, Hirano M, Marti I, Martin MA, Munell F, Nascimento A, Olive M, Quan J, Sardina MD, Marti R, Paradas C. Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency. Orphanet Journal of Rare Diseases. 2021; 16(1):407. DOI:10.1186/s13023-021-02030-w. PMID:34600563. IF: 4,303
Fionda L, Turon J, Prior PF, Noguera SB, Cortes E, Lopez MA, Gallardo E, Rojas R. A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?. JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 2021; 26(1). DOI:10.1111/jns.12425. PMID:33320396. IF: 5,188
Frasquet M, Rojas R, Argente H, Vazquez JF, Muelas N, Vilchez JJ, Sivera R, Millet E, Barreiro M, Diaz J, Turon J, Cortes E, Querol L, Ramirez L, Martinez D, Sanchez A, Espinos C, Sevilla T, Lupo V. Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation. EUROPEAN JOURNAL OF NEUROLOGY. 2021; 28(4). DOI:10.1111/ene.14700. PMID:33369814. IF: 6,288
Gelber PE, Ramirez E, Grau A, Gonzalez A, Llauger J, Farinas O. A new computed tomography scoring system to assess osteochondral allograft transplantation for the knee: inter-observer and intra-observer agreement. INTERNATIONAL ORTHOPAEDICS. 2021; 45(5). DOI:10.1007/s00264-020-04927-w. PMID:33416905. IF: 3,479
Gutschmidt K, Musumeci O, Diaz J, Chien YH, Knop KC, Wenninger S, Montagnese F, Pugliese A, Tavilla G, Alonso J, Hwu PWL, Toscano A, Schoser B. STIG study: real-world data of long-term outcomes of adults with Pompe disease under enzyme replacement therapy with alglucosidase alfa. JOURNAL OF NEUROLOGY. 2021; 268(7). DOI:10.1007/s00415-021-10409-9. PMID:33543425. IF: 6,682
Jacobs MB, James MK, Lowes LP, Alfano LN, Eagle M, Lofra RM, Moore U, Feng J, Rufibach LE, Rose K, Duong T, Bello L, Pedrosa I, Holsten S, Sakamoto C, Canal A, Praxedes N, Thiele S, Siener C, Vandevelde B, DeWolf B, Maron E, Guglieri M, Hogrel JY, Blamire AM, Carlier PG, Spuler S, Day JW, Jones KJ, Bharucha DX, Salort E, Pestronk A, Walter MC, Et al. [Diaz J]. Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale. ANNALS OF NEUROLOGY. 2021; 89(5). DOI:10.1002/ana.26044. PMID:33576057. IF: 11,274
Lleixa C, Martin L, Pascual E, Franco T, Caballero M, De Luna N, Gallardo E, Suarez X, Martinez L, Diaz J, Rojas R, Cortes E, Turon J, Casasnovas C, Homedes C, Gutierrez G, Jimeno MC, Berciano J, Sedano MJ, Garcia T, Pardo J, Marquez C, Rojas I, Jerico I, Martinez E, de la Tassa GM, Dominguez C, Juarez C, Illa I, Querol L. Autoantibody screening in Guillain-Barre syndrome. Journal of Neuroinflammation. 2021; 18(1):251. DOI:10.1186/s12974-021-02301-0. PMID:34719386. IF: 9,587
Luijten LWG, Leonhard SE, van der Eijk AA, Doets AY, Appeltshauser L, Arends S, Attarian S, Benedetti L, Briani C, Casasnovas C, Castellani F, Dardiotis E, Echaniz A, Garssen MPJ, Harbo T, Huizinga R, Humm AM, Jellema K, van der Kooi AJ, Kuitwaard K, Kuntzer T, Kusunoki S, Lascano AM, Martinez E, Rinaldi S, Samijn J, Scheidegger O, Tsouni P, Vicino A, Visser LH, Walgaard C, Wang YZ, Wirtz PW, Ripellino P, Jacobs BC, Martín L, Živkovic SA. Guillain-Barre syndrome after SARS-CoV-2 infection in an international prospective cohort study. BRAIN. 2021; 144(11). DOI:10.1093/brain/awab279. PMID:34553216. IF: 15,255
Mantegazza R, Wolfe GI, Muppidi S, Wiendl H, Fujita KP, O’Brien FL, Booth H, Howard JF, Illa I, Cortés E, Díaz J, Querol LA, Rojas R, Vidal N, RSG. Post-intervention Status in Patients With Refractory Myasthenia Gravis Treated With Eculizumab During REGAIN and Its Open-Label Extension. 2021; 96(4). DOI:10.1212/WNL.0000000000011207. PMID:33229455. IF: 11.800
Martel L, Alonso A, Bascunana H, Diaz J, Llauger J, Nunez C, Montesinos P, Webb SM, Valassi E. Prevalence of sarcopenia after remission of hypercortisolism and its impact on HRQoL. CLINICAL ENDOCRINOLOGY. 2021; 95(5). DOI:10.1111/cen.14568. PMID:34323296. IF: 3,523
Martel L, Alonso J, Bascunana H, Diaz J, Llauger J, Nunez C, Montesinos P, Webb SM, Valassi E. Intramuscular fatty infiltration and physical function in controlled acromegaly. EUROPEAN JOURNAL OF ENDOCRINOLOGY. 2021; 185(1). DOI:10.1530/EJE-21-0209. PMID:33950861. IF: 6,558
Martin L, Camps P, Lleixa C, Pascual E, Diaz J, Rojas R, De Luna N, Gallardo E, Cortes E, Munoz L, Alcolea D, Lleo A, Casasnovas C, Homedes C, Gutierrez G, Jimeno MC, Berciano J, Sedano MJ, Garcia T, Pardo J, Marquez C, Rojas I, Jerico I, Martinez E, de la Tassa GM, Dominguez C, Illa I, Querol L. Serum neurofilament light chain predicts long-term prognosis in Guillain-Barre syndrome patients. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 2021; 92(1). DOI:10.1136/jnnp-2020-323899. PMID:33154183. IF: 13,654
Meca JE, Maurino J, Perez F, Forero L, Sepulveda M, Calles C, Martinez ML, Gonzalez I, Boyero S, Romero L, Sempere AP, Meca V, Querol L, Costa L, Prefasi D, Gomez R, Ballesteros J. Quantifying the patient ‘ s perspective in neuromyelitis optica spectrum disorder: Psychometric properties of the SymptoMScreen questionnaire. PLoS One. 2021; 16(7):e0255317. DOI:10.1371/journal.pone.0255317. PMID:34324586. IF: 3,752
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Narayanaswami P, Sanders DB, Wolfe G, Benatar M, Cea G, Evoli A, Gilhus NE, Illa I, Kuntz NL, Massey J, Melms A, Murai H, Nicolle M, Palace J, Richman D, Verschuuren J. International Consensus Guidance for Management of Myasthenia Gravis 2020 Update. 2021; 96(3). DOI:10.1212/WNL.0000000000011124. PMID:33144515. IF: 11,800
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ENFERMEDADES NEUROLóGICAS, NEUROCIENCIA Y SALUD MENTAL

Enfermedades Neuromusculares

Principales líneas de investigación

Enfermedades neuromusculares inmunomediadas

Distrofia muscular, disferlinopatía y miopatías distales

Esclerosis lateral amiotrófica

Retos

Información adicional : Neuromuscularbcn

Coordinación del grupo

Miembros

Publicaciones 2022

Publicaciones 2021

Principales líneas de investigación

Enfermedades neuromusculares inmunomediadas

Distrofia muscular, disferlinopatía y miopatías distales

Esclerosis lateral amiotrófica

Retos

Información adicional : Neuromuscularbcn

Coordinación del grupo

Miembros

Publicaciones 2022

Publicaciones 2021

Institut de Recerca de l’Hospital de la Santa Creu i Sant Pau