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Letter to the editor
Beyond the Classic Segawa Disease, GCH1-Associated Neurodegenerative Parkinsonism: Practical Considerations for Physicians
Jirat Chenbhanich, Jirada Sringean, Roongroj Bhidayasiri
J Mov Disord. 2017;10(2):102-104.   Published online April 18, 2017
DOI: https://doi.org/10.14802/jmd.17009
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Citations to this article as recorded by  
  • Comprehensive Analysis of Familial Parkinsonism Genes in Rapid‐Eye‐Movement Sleep Behavior Disorder
    Kheireddin Mufti, Uladzislau Rudakou, Eric Yu, Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent, Dan Spiegelman, Isabelle Arnulf, Michele T.M. Hu, Jacques Y. Montplaisir, Jean‐François Gagnon, Alex Desautels, Yves Dauvilliers, Gian Luigi
    Movement Disorders.2021; 36(1): 235.     CrossRef
  • Differences in Drug Pharmacokinetics and Motor Fluctuation in DYT-GCH1
    Gerard Saranza, Anthony E. Lang
    Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.2021; 48(5): 734.     CrossRef
  • A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia
    Subhajit Giri, Tufan Naiya, Shubhrajit Roy, Gautami Das, Gurusidheshwar M. Wali, Shyamal Kumar Das, Kunal Ray, Jharna Ray
    Journal of Molecular Neuroscience.2019; 68(2): 214.     CrossRef
  • Common and rare GCH1 variants are associated with Parkinson disease
    Uladzislau Rudakou, Bouchra Ouled Amar Bencheikh, Jennifer A. Ruskey, Lynne Krohn, Sandra B. Laurent, Dan Spiegelman, Christopher Liong, Stanley Fahn, Cheryl Waters, Oury Monchi, Edward A. Fon, Yves Dauvilliers, Roy N. Alcalay, Nicolas Dupré, Ziv Gan-Or
    Neurobiology of Aging.2018;[Epub]     CrossRef

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