Jose Gazulla-Abio

Zaragoza, AR, Spain

Last Updated: 09/26/2026

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Found 58 publications

Classic Guillain-Barré syndrome.

Classic Guillain-Barré syndrome.

Journal: Medicina clinica

Published: December 13, 2024

Potential Clinical Benefit of Very Long Chain Fatty Acid Supplementation in Spinocerebellar Ataxia Type 34.

Potential Clinical Benefit of Very Long Chain Fatty Acid Supplementation in Spinocerebellar Ataxia Type 34.

Journal: Cerebellum (London, England)

Published: May 13, 2024

External Laryngeal Tremor in Adult-Onset Alexander Disease: A Case Report.

External Laryngeal Tremor in Adult-Onset Alexander Disease: A Case Report.

Journal: Case reports in neurology

Published: March 05, 2024

Potential Benefit of Channel Activators in Loss-of-Function Primary Potassium Channelopathies Causing Heredoataxia.

Potential Benefit of Channel Activators in Loss-of-Function Primary Potassium Channelopathies Causing Heredoataxia.

Journal: Cerebellum (London, England)

Published: June 29, 2023

Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy.

Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: March 15, 2023

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

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

Journal: European journal of neurology

Published: November 17, 2022

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

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

Journal: European journal of medical genetics

Published: July 14, 2022

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

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

Journal: Journal of neurology

Published: March 15, 2022

CANVAS is an Oligosymptomatic Disease.

CANVAS is an Oligosymptomatic Disease.

Journal: Annals of Indian Academy of Neurology

Published: October 15, 2021

History of Ataxias and Paraplegias with an Annotation on the First Description of Striatonigral Degeneration.

History of Ataxias and Paraplegias with an Annotation on the First Description of Striatonigral Degeneration.

Journal: Cerebellum (London, England)

Published: September 20, 2021

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

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

Journal: European journal of neurology

Published: September 06, 2021

Gabapentin Relieves Vertigo of Periodic Vestibulocerebellar Ataxia: 3 Cases and Possible Mechanism.

Gabapentin Relieves Vertigo of Periodic Vestibulocerebellar Ataxia: 3 Cases and Possible Mechanism.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: April 20, 2021

Showing 1-12 of 58

Last Updated: 09/26/2026