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Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutationsLorraine N Clark, Shehla Afridi, Helen Mejia-Santana, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 16, 2015
Strategies for treatment of dystoniaDirk Dressler, Eckart Altenmueller, Roongroj Bhidayasiri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin geneLorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 5, 2008
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutationsDeborah Raymond, Rachel Saunders-Pullman, Patricia de Carvalho Aguiar, et al.
The Journal of Clinical Psychiatry|July 8, 2011
An international consensus study of neuroleptic malignant syndrome diagnostic criteria using the Delphi methodRonald J Gurrera, Stanley N Caroff, Abigail Cohen, et al.
Clinical Parkinsonism & Related Disorders|July 28, 2021
Targeting neurons in the gastrointestinal tract to treat Parkinson's diseaseRobert A Hauser, Dean Sutherland, Juan A Madrid, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Integrated Stress Response Signatures Drive Monocyte Dysfunction in GBA1- and LRRK2-Linked Parkinson's DiseaseDaniele Mattei, Erica Brophy, Mikaela Rosen, et al.
Research Square|February 27, 2026
Integrated Stress Response Signatures Drive Monocyte Dysfunction in GBA1- and LRRK2-Linked Parkinson's DiseaseDaniele Mattei, Erica Brophy, Mikaela Rosen, et al.
Archives of Neurology|September 15, 2010
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease studyRoy N Alcalay, Elise Caccappolo, Helen Mejia-Santana, et al.
American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
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