Hereditary progressive dystonia with marked diurnal fluctuation
- 30 September 2000
- journal article
- review article
- Published by Elsevier in Brain & Development
- Vol. 22, 65-80
- https://doi.org/10.1016/s0387-7604(00)00148-0
Abstract
No abstract availableKeywords
This publication has 51 references indexed in Scilit:
- Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismNature, 1998
- The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14qAnnals of Neurology, 1995
- A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndromeHuman Genetics, 1995
- Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I geneNature Genetics, 1994
- Dopa‐responsive dystonia: Pathological and biochemical observations in a caseAnnals of Neurology, 1994
- Dopa-responsive dystoniaAnnals of Neurology, 1994
- Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14qNature Genetics, 1993
- Tyrosine hydroxylase and levodopa responsive dystonia.Journal of Neurology, Neurosurgery & Psychiatry, 1989
- DOPA-Sensitive Progressive Dystonia of Childhood with Fluctuations of Symptoms - Segawa's Syndrome and Possible Variants*Neuropediatrics, 1986
- Paralysis agitans of early onset with marked diurnal fluctuation of symptomsNeurology, 1973