Ivonne Jericó

Specific HLA-DRB1 Alleles Associate With Anti-Caspr1 and Anti-CNTN1 Autoantibodies in Autoimmune Nodopathies

Cinta Lleixà, Elba Pascual‐Goñi, L. Aguilar, Marta Caballero‐Ávila et autres

es, gb, it, fr, at, be, de, nl, ch (code pays fourni par la source)

Advanced magnetic resonance imaging as a biomarker to differentiate Primary lateral sclerosis from Amyotrophic lateral sclerosis

Maialen Imizcoz, T. Cabada, Juan Quizhpilema, Amaia Erdocia et autres

ca, es (code pays fourni par la source)

Variably Protease‐Sensitive Prionopathy: Two New Cases With Motor Neuron‐Dementia Syndrome

María Elena Erro, María Victoria Zelaya, Hasier Eraña, Javier Sanchez Ruiz de Gordoa et autres

es, at (code pays fourni par la source)

Asymmetric white matter degeneration in amyotrophic lateral sclerosis: a diffusion kurtosis imaging study of motor and extra-motor pathways

Juan Carlos Quizhpilema, Ane Legarda, José Manuel Hidalgo, Pablo Lecumberri et autres

es (code pays fourni par la source)

Cost analysis of treatment with therapeutic plasma exchange versus treatment with intravenous immunoglobulins in patients with immune-based neurological diseases. Proposal for optimising the use of plasmatic blood products

M. Luisa Antelo, Saioa Zalba Marcos, Ivonne Jericó, M. Sarobe et autres

es (code pays fourni par la source)

Advancing Personalized Medicine in Alzheimer’s Disease: Liquid Biopsy Epigenomics Unveil APOE ε4-Linked Methylation Signatures

Mónica Macías, Juan José Alba‐Linares, Blanca Acha, Idoia Blanco‐Luquin et autres

es (code pays fourni par la source)

A founder variant in the RYR1 gene is associated with hyperCKemia , myalgia and muscle cramps

Alba Segarra‐Casas, Pablo Iruzubieta, Solange Kapetanovic, Aurelio Hernández‐Laín et autres

es, gb (code pays fourni par la source)

Towards a Personalized Medicine through Liquid Biopsy in Alzheimer’s disease: Epigenome of cell-free DNA reveals methylation differences linked to APOE status

Mónica Macías, Juan José Alba‐Linares, Blanca Acha, Idoia Blanco‐Luquin et autres

es (code pays fourni par la source)

20733. HISTORIA NATURAL DE PACIENTES CON ATROFIA MUSCULAR ESPINAL CON 3 Y 4 COPIAS DEL GEN SMN2. DATOS DEL REGISTRO NACIONAL ESPAÑOL (CUIDAME)

L. Puig Cruz, K. Aragón Gawinska, María Fernández García, A. Osorio et autres

Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy

Ellen Gelpí, Raphael Reinecke, Carles Gaig, Álex Iranzo et autres

at, es, si, de, it, fi, nl, gb, ca, us (code pays fourni par la source)

202P Descriptive analysis of the spinal muscular atrophy population treated with Nusinersen included in the CuidAME project

J. Sotoca Fernandez, C. Martínez Puig, Rocio García-Uzquiano, María Teresa García‐Romero et autres

es (code pays fourni par la source)

201P Natural history of spinal muscular atrophy patients with 3 and 4 copies of SMN2 gene – data from the national Spanish registry (CUIDAME)

K. Aragón Gawinska, María Fernández García, Andres Nascimiento Osorio, Carmen Paradas et autres