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Ali H Rajput

Showing results (71-80 of 78) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expressionChristian Wider, Justus C Dachsel, Alexandra I Soto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2004
Levodopa in the treatment of Parkinson's disease: current controversiesC Warren Olanow, Yves Agid, Yoshi Mizuno, et al.
Nature Genetics|June 9, 2016
Identification of TMEM230 mutations in familial Parkinson's diseaseHan-Xiang Deng, Yong Shi, Yi Yang, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

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Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expressionChristian Wider, Justus C Dachsel, Alexandra I Soto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2004
Levodopa in the treatment of Parkinson's disease: current controversiesC Warren Olanow, Yves Agid, Yoshi Mizuno, et al.
Nature Genetics|June 9, 2016
Identification of TMEM230 mutations in familial Parkinson's diseaseHan-Xiang Deng, Yong Shi, Yi Yang, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
Pageof 8