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Movement Disorders Clinical Practice|March 7, 2019
Novel Nonsense Calmodulin-Binding Transcription Activator 1 Mutation Presenting as a Tremor-Predominant PhenotypeShashank Agarwal, Rebecca Gilbert, Heather A LauMovement Disorders Clinical Practice|March 7, 2019
Neurodegeneration With Brain Iron Accumulation (NBIA) Syndromes Presenting With Late-Onset Craniocervical Dystonia: An Illustrative Case SeriesFlorian Brugger, Georg Kägi, Massimo Pandolfo, et al.Movement Disorders Clinical Practice|March 7, 2019
Tremor-Dominant Pantothenate Kinase-associated NeurodegenerationMohammad Rohani, Gholamali Shahidi, Afagh Alavi, et al.Movement Disorders Clinical Practice|March 7, 2019
Defining Palliative Care Needs in Parkinson's DiseaseBenzi M Kluger, Jo Shattuck, Julie Berk, et al.Movement Disorders Clinical Practice|March 7, 2019
A Scale to Assess Activities of Daily Living in Pantothenate Kinase-Associated NeurodegenerationRandall D Marshall, Abigail Collins, Maria L Escolar, et al.Movement Disorders Clinical Practice|March 7, 2019
How Do I Manage Patients With the Levodopa/Carbidopa Intestinal Gel?Nirosen Vijiaratnam, Carolyn M SueMovement Disorders Clinical Practice|October 27, 2018
Ataxia Telangiectasia Gene Mutation in Isolated Segmental Dystonia Without Ataxia and TelangiectasiaJán Necpál, Michael Zech, Matej Škorvánek, et al.Movement Disorders Clinical Practice|October 27, 2018
Clinical Characterization of Genetically Diagnosed Cases of Spinocerebellar Ataxia Type 12 from IndiaSupriyo Choudhury, Sayan Chatterjee, Koustav Chatterjee, et al.Movement Disorders Clinical Practice|October 27, 2018
Deep Brain Stimulation for the Dystonias: Evidence, Knowledge Gaps, and Practical ConsiderationsRené Reese, Jens VolkmannMovement Disorders Clinical Practice|October 27, 2018
The Corpus Callosum Splenium Sign in Fragile X-Associated Tremor Ataxia SyndromeDeborah A Hall, Meghan Hermanson, Emily Dunn, et al.Pageof 152