Immune response and safety of SARS-CoV-2 mRNA-1273 vaccine in patients with myasthenia gravis D Reyes-Leiva, J López-Contreras, E Moga, F Pla-Juncà, E Lynton-Pons, ... Neurology: Neuroimmunology & Neuroinflammation 9 (4), e200002, 2022 | 18 | 2022 |
Rituximab treatment in myasthenia gravis A Vesperinas-Castro, E Cortés-Vicente Frontiers in Neurology 14, 1275533, 2023 | 3 | 2023 |
Clinicopathological correlates in frontotemporal lobar degeneration: motor neuron disease spectrum Á Carbayo, S Borrego-Écija, J Turon-Sans, E Cortés-Vicente, ... Brain, awae011, 2024 | 1 | 2024 |
Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene P Martín-Jiménez, A Hernández-Laín, A Arteche-López, ... Muscle & nerve 66 (4), E13-E15, 2022 | 1 | 2022 |
Frequency, Predictors, Etiology, and Outcomes for Deep Intracerebral Hemorrhage without Hypertension L Prats-Sánchez, P Iruzubieta, A Vesperinas, R Collet, ... Journal of Stroke and Cerebrovascular Diseases 31 (3), 106293, 2022 | 1 | 2022 |
Membrane Proteome-Wide Screening of Autoantibodies in CIDP Using Human Cell Microarray Technology M Caballero-Ávila, C Lleixà, E Pascual-Goñi, L Martín-Aguilar, ... Neurology: Neuroimmunology & Neuroinflammation 11 (3), e200216, 2024 | | 2024 |
A homozygous ATP2A2 variant alters sarcoendoplasmic reticulum Ca2+-ATPase 2 function in skeletal muscle and causes a novel vacuolar myopathy L Llanso, G Ravenscroft, C Aceituno, A Gutierrez, J Parmar, P Gallano, ... medRxiv, 2024.05. 14.24307284, 2024 | | 2024 |
Antibodies against the flotillin-1/2 complex in patients with multiple sclerosis C Lleixà, M Caballero-Ávila, E Pascual-Goñi, L Martín-Aguilar, N Vidal, ... Brain Communications 5 (2), fcad109, 2023 | | 2023 |
A new homozygous missense variant in LMOD3 gene causing mild nemaline myopathy with prominent facial weakness A Segarra-Casas, R Collet, L Gonzalez-Quereda, A Vesperinas, ... Neuromuscular Disorders 33 (4), 319-323, 2023 | | 2023 |
BRAIN COMMUNICATIONS C Lleixà, M Caballero-Ávila, E Pascual-Goñi, L Martín-Aguilar, N Vidal, ... | | 2023 |
P. 156 Novel repeat expansions in PLIN4 in two Spanish families suffering from autosomal dominant distal myopathy with unique pathological features M Olivé, I Stevanovski, LG Quereda, G Morris, A Segarra-Casas, ... Neuromuscular Disorders 32, S110, 2022 | | 2022 |
P. 02 Mild nemaline myopathy 10 caused by a novel missense homozygous mutation in LMOD3: broadening the phenotype-genotype correlation A Segarra-Casas, L Gonzalez-Quereda, M Caballero, M Rodriguez, ... Neuromuscular Disorders 32, S45, 2022 | | 2022 |
SEARCHING FOR POTENTIAL BIOMARKERS IN GUILLAIN-BARRe SYNDROME: CALPROTECTIN AND PERIPHERAL MYELIN PROTEIN 2 M Caballero-avila, C Lleixa, L Martin-Aguilar, E Pascual-Goni, ... JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 27, S19-S20, 2022 | | 2022 |