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Ana Vesperinas
Ana Vesperinas
Verified email at santpau.cat - Homepage
Title
Cited by
Cited by
Year
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
182022
Rituximab treatment in myasthenia gravis
A Vesperinas-Castro, E Cortés-Vicente
Frontiers in Neurology 14, 1275533, 2023
32023
Clinicopathological correlates in frontotemporal lobar degeneration: motor neuron disease spectrum
Á Carbayo, S Borrego-Écija, J Turon-Sans, E Cortés-Vicente, ...
Brain, awae011, 2024
12024
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
12022
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
12022
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
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