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The metabolic pathology of dopa-responsive dystonia

Published:2005 Issue:4 Volume:57 Page:596-600
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Asanuma Kotaro,Ma Yilong,Huang Chaorui,Carbon-Correll Maren,Edwards Christine,Raymond Deborah,Bressman Susan B.,Moeller James R.,Eidelberg David

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference20 articles.

1. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease)

2. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

3. Dystonia: clinical features, genetics, and treatment

4. Dopa-responsive dystonia: Pathological and biochemical observations in a case

5. Striatal biopterin and tyrosine hydroxylase protein reduction in dopa-responsive dystonia

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3. Time estimation and arousal responses in dopa-responsive dystonia;Scientific Reports;2022-08-22

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