Información del personal investigador

Authorship: CINTA LLEIXA, LORENA MARTÍN AGUILAR, ELBA PASCUAL GOÑI, TERESA FRANCO, MARTA CABALLERO, NOEMÍ DE LUNA, EDUARD GALLARDO, XAVIER SUÁREZ CALVET, LAURA MARTÍNEZ MARTÍNEZ, JORDI DIAZ MANERA, RICARD ROJAS GARCÍA, ELENA CORTÉS VICENTE, JOANA TURÓN, CARLOS CASASNOVAS, CHRISTIAN HOMEDES, GERARDO GUTIÉRREZ GUTIÉRREZ, MARÍA CONCEPCIÓN JIMENO MONTERO, JOSE ANGEL BERCIANO BLANCO, MARIA JOSE SEDANO TOUS, TANIA GARCÍA SOBRINO

01/11/2021

Ia afferent fibers in peripheral nerve disorders: evidence for divergent vulnerability

Article

Clinical Neurophysiology Practice, 2021, 6, 133-134

Authorship: ANTONIO GARCÍA, JON INFANTE CEBERIO, JOSE ANGEL BERCIANO BLANCO

01/04/2021

Linfoma primario del sistema nervioso central aparentando lesión del ángulo pontocerebeloso

Article

Neurología, 2020, 35(7), 506-507

Authorship: JOSE ANGEL BERCIANO BLANCO

01/09/2020

Spinal nerve pathology in Guillain-Barré syndrome associated with COVID-19 infection

Article

Muscle & Nerve. 2020;volume 62, Issue 5 :E74-E75

Authorship: JOSE ANGEL BERCIANO BLANCO, ELENA CARMEN GALLARDO AGROMAYOR

01/11/2020

POLR3A-related spastic ataxia: new mutations and a look into the phenotype

Article

Journal of Neurology, 2020, 267(2), 324-330

Authorship: JON INFANTE CEBERIO, KARLA M. SERRANO-CÁRDENAS, MARC CORRAL-JUAN, XAVIER FARRÉ, IVELISSE SÁNCHEZ, ENRIQUE M. DE LUCAS, ANTONIO GARCÍA, JOSÉ LUIS MARTÍN-GURPEGUI, JOSE ANGEL BERCIANO BLANCO, ANTONI MATILLA-DUEÑAS

01/02/2020

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Portal del personal investigador

JOSE ANGEL BERCIANO BLANCO

Identifiers

Comment on "Spectrum disorder of RFC1 expansions/CANVAS: clinical and electrophysiological characterization of a group of 31 patients"

Correo electrónico institucional o correo personal en los manuscritos enviados a las revistas biomédicas: el caso de los médicos jubilados

Acute inflammatory demyelinating polyneuropathy shortly after administration of intravitreal ranibizumab: a clinical and electrophysiological annotation

Síndrome de Guillain-Barré clásico

Potential benefit of channel activators in loss-of-function primary potassium channelopathies causing heredoataxia

Letter to the editor regarding "Immune-inflammation mapping in Guillain-Barré syndrome"

The pathophysiological role of endoneurial inflammatory edema in early classical Guillain-Barré syndrome

Potential clinical benefit of very long chain fatty acid supplementation in spinocerebellar ataxia type 34

External laryngeal tremor in adult-onset Alexander disease: a case report

Pathophysiology and markers of very early classic Guillain-Barré syndrome

Microscopical anatomy of the peripheral nervous system: an essential notion for understanding the pathophysiology of very early classic Guillain-Barré syndrome

Guillain?Barré Syndrome with Normal Nerve Conduction Study Associated with COVID-19 Infection in a Child: correspondence

Spinocerebellar ataxia type 15 caused by missense variants in the ITPR1 gene

Ataxia de Marie: en recuerdo de un epónimo clásico caído en desuso

Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: supplementary evidence for a continuum

History of ataxias and paraplegias with an annotation on the first description of striatonigral degeneration

Patología axonal en la fase precoz del síndrome de Guillain-Barré

Two-year follow-up of docosahexaenoic acid supplementation in spinocerebellar ataxia type 38 (SCA38)

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022)

Autoantibody screening in Guillain-Barré syndrome

Ia afferent fibers in peripheral nerve disorders: evidence for divergent vulnerability

Linfoma primario del sistema nervioso central aparentando lesión del ángulo pontocerebeloso

Spinal nerve pathology in Guillain-Barré syndrome associated with COVID-19 infection

POLR3A-related spastic ataxia: new mutations and a look into the phenotype