Citation Tools
PDF
Other content recommended for you
- Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients
- Frequency of GCH1 deletions in Dopa-responsive dystonia
- Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency
- Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm
- Older-onset levodopa-responsive parkinsonism with normal DAT-SPECT and pterin hypometabolism
- Dramatic levodopa responsiveness of dystonia in a sporadic case of spinocerebellar ataxia type 3
- Clinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene
- GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness
- Parkinson's disease
- Two in the hand, an essential lesson in tremor management