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spinocerebellar ataxias 2
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Curated Studies
Most Correlated Studies
Neurons from iPSCs generated from dermal fibroblasts/PBMCs of spinocerebellar ataxia 2 and 3 patient
OMIM - Congenital disorder
Cerebella, midbrains and livers from 6mo, 12mo and 24mo old ATXN2 knockout mice
Neural progenitors from Friedreich ataxia patient iPSCs (induced pluripotent stem cells)
Frataxin deficiency in a Friedreich Ataxia mouse model is corrected by HDAC inhibitor
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Literature
Most Relevant Literature
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian…
Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.
Dopa-responsive dystonia in spinocerebellar ataxia 6: A case report.
Spinocerebellar ataxia 2 develop lower motor neuron involvement as an initial symptom: a case report…
Severe Neurodevelopmental Disorder in Autosomal Recessive Spinocerebellar Ataxia 13 (SCAR13) Caused …
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Clinical Trials
Most Relevant Clinical Trials
Safety and Tolerability of Lithium in Spinocerebellar Ataxia 2 (SCA2)
Clinical Trial With Riluzole in Spinocerebellar Ataxia Type 2 (ATRIL)
Dalfampridine and Gait in Spinocerebellar Ataxias
Study of CAD-1883 for Spinocerebellar Ataxia
Functional and Structural Imaging and Motor Control in Spinocerebellar Ataxia
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