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Last Updated : 06/20/2022

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Found 51 publications

Safety and efficacy of riluzole in spinocerebellar ataxia type 2 in France (ATRIL): a multicentre, randomised, double-blind, placebo-controlled trial.

Spinocerebellar ataxia 17: full phenotype in a 42 CAG/CAA-repeats carrier.

Possibilities and challenges of small molecule organic compounds for the treatment of repeat diseases.

Vocal cord paralysis as a presenting sign of autosomal recessive spinocerebellar atrophy type 10.

Spinocerebellar ataxia type 28 in a Chinese pedigree: A case report and literature review.

Proteomic Analysis of Marinesco-Sjogren Syndrome Fibroblasts Indicates Pro-Survival Metabolic Adaptation to SIL1 Loss.

Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia.

Cortical and Subcortical Brain Area Atrophy in SCA1 and SCA2 Patients in India: The Structural MRI Underpinnings and Correlative Insight Among the Atrophy and Disease Attributes.

Nystagmus may be the first neurological sign in early stages of spinocerebellar ataxia type 3.

Cerebellar degeneration in primary Sjögren syndrome: a case report.

CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells.

Mutations in the Voltage Dependent Calcium Channel CACNA1A (P/Q type alpha 1A subunit) Causing Neurological Disorders - An Overview.

Showing 1-12 of 51

Last Updated : 06/20/2022