Segawa disease

Clinical Neurology

Volumn 37, Issue 12, 1997, Pages 1137-1138

  Nomura, Yoshiko ^a  

^a Segawa Neurol Clinic for Children

Author keywords

GTP cyclohydrolase I; Postural dystonia; Segawa disease; Tetrahydrobiopterin (BH4); Tyrosine hydroxylase (TH)

Indexed keywords

6 FLUORODOPA; BIOPTERIN; DOPAMINE; DOPAMINE 1 RECEPTOR; DOPAMINE 2 RECEPTOR; DOPAMINE RECEPTOR; GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE I; LEVODOPA; NEOPTERIN; PTERIN DERIVATIVE; RACLOPRIDE; TETRAHYDROBIOPTERIN; TYROSINE 3 MONOOXYGENASE;

AUTOSOMAL DOMINANT DISORDER; CONFERENCE PAPER; DYSTONIA; GENE MUTATION; HUMAN; PES EQUINOVARUS; POSITRON EMISSION TOMOGRAPHY; SEGAWA DISEASE; TREMOR;

ADOLESCENT; ADULT; DYSTONIA; FEMALE; HUMANS; MALE;

EID: 0031447902     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (3)

1. Segawa M, Nomura Y : Pathophysiology of hereditary progressive dystonia with marked diurnal fluctuation - its characteristics in contrast to other dopa responsive disorders. In Progress in Alzheimer's and Parkinson's disease, ed by Fisher M, Yoshida M, Hanin I, Plenum (in press)
2. Nomura Y, Uetake K, Yukishita S, et al : Dystonias responding to levodopa and failure in biopterin metabolism. In Advances in neurology, Lippincott-Raven (in press)
3. Ichinose H, Ohye T, Takahashi E, et al : Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nature Geneti 8. 236-242, 1994