Fragile X-associated tremor/ataxia syndrome and movements disorders
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference43 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
2. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
3. Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome
4. Absence of expression of the FMR-1 gene in fragile X syndrome
5. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
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1. DeepBhvTracking: A Novel Behavior Tracking Method for Laboratory Animals Based on Deep Learning;Frontiers in Behavioral Neuroscience;2021-10-28
2. A Chinese case of fragile X-associated tremor/ataxia syndrome (FXTAS) with orthostatic tremor:case report and literature review on tremor in FXTAS;BMC Neurology;2020-04-20
3. Abordagem clínica de pacientes com ataxia;Revista Neurociências;2019-01-23
4. Genetic mimics of the non-genetic atypical parkinsonian disorders – the ‘atypical’ atypical;International Review of Neurobiology;2019
5. Tremor and myoclonus;Handbook of Clinical Neurology;2019
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