Fragile X gene premutation in multiple system atrophy
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference21 articles.
1. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X;Hagerman;Neurology,2001
2. A cerebellar tremor/ataxia syndrome among fragile X premutation carriers;Hagerman;Cytogenet. Genome Res.,2003
3. Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia;Macpherson;Hum. Genet.,2003
4. The fragile X premutation presenting as essential tremor;Leehey;Arch. Neurol.,2003
5. Consensus statement on the diagnosis of multiple system atrophy;Gilman;J. Neurol. Sci.,1999
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1. Frequency of FMR1 Premutation Alleles in Patients with Undiagnosed Cerebellar Ataxia and Multiple System Atrophy in the Japanese Population;The Cerebellum;2021-11-29
2. Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism;Neurological Research;2021-01-06
3. Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Pathophysiology and Clinical Implications;International Journal of Molecular Sciences;2020-06-20
4. Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders;The Clinical Neuropsychologist;2016-07-14
5. The Epidemiology of FXTAS;FXTAS, FXPOI, and Other Premutation Disorders;2016
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