Nonmotor Symptoms in Dopa-Responsive Dystonia

Author:

Antelmi Elena12,Stamelou Maria34ORCID,Liguori Rocco15,Bhatia Kailash P.2

Affiliation:

1. Department of Biomedical and Neuromotor Sciences; Alma Mater Studiorum; University of Bologna; Bologna Italy

2. Sobell Department of Motor Neuroscience and Movement Disorders; University College London (UCL) Institute of Neurology; London United Kingdom

3. Second Department of Neurology; University of Athens; Athens Greece

4. Neurology Clinic; Philipps University; Marburg Germany

5. IRCCS Institute of Neurological Sciences; Bologna Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference84 articles.

1. Chilhood basal ganglia disease with remarkable response to l-dopa: hereditary basal ganglia disease with marked diurnal fluctuation (in Japanese);Segawa;Shinryo (Tokyo),1971

2. Phenomenology and classification of dystonia: a consensus update;Albanese;Mov Disord,2013

3. Dopa-responsive dystonia. Delineation of the clinical syndrome and clues to pathogenesis;Nygard;Adv Neurol,1993

4. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene;Ichinose;Nat Genet,1994

5. Genetics and biochemistry of dopa-responsive dystonia: significance of striatal tyrosine hydroxylase protein loss;Furukawa;Adv Neurol,2003

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