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Journal Articles

in Movement Disorders
 41-32 of 32 Articles

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JAMA Neurology
Original Investigation  | 
The Phosphodiesterase 10 Positron Emission Tomography Tracer, [18F]MNI-659, as a Novel Biomarker for Early Huntington Disease
David S. Russell, MD, PhD; Olivier Barret, PhD; Danna L. Jennings, MD; et al.
JAMA Neurology
Original Investigation  | 
Amyotrophic Lateral Sclerosis Risk for Spinocerebellar Ataxia Type 2 ATXN2 CAG Repeat Alleles:  A Meta-analysis
Annalese G. Neuenschwander; Khanh K. Thai, MS; Karla P. Figueroa, MS; et al.
JAMA Neurology
Case Report/Case Series  | 
Autosomal Recessive Cerebellar Ataxia Type 3 Due to ANO10 Mutations:  Delineation and Genotype-Phenotype Correlation Study
Mathilde Renaud, MD; Mathieu Anheim, MD, PhD; Erik-Jan Kamsteeg, PhD; et al.
JAMA Neurology
Original Investigation  | 
Exome Sequencing in the Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia
Brent L. Fogel, MD, PhD; Hane Lee, PhD; Joshua L. Deignan, PhD; et al.