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Christian Wider

Showing results (41-50 of 52) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Parkinsonism & Related Disorders|August 30, 2008
Pallidonigral TDP-43 pathology in Perry syndromeChristian Wider, Dennis W Dickson, A Jon Stoessl, et al.
Parkinsonism & Related Disorders|September 2, 2009
LINGO1 rs9652490 is associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Owen A Ross, Christian Wider, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.
Neurogenetics|April 7, 2010
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's diseaseJan O Aasly, Carles Vilariño-Güell, Justus C Dachsel, et al.
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.
Nature Genetics|January 13, 2009
DCTN1 mutations in Perry syndromeMatthew J Farrer, Mary M Hulihan, Jennifer M Kachergus, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Parkinsonism & Related Disorders|August 30, 2008
Pallidonigral TDP-43 pathology in Perry syndromeChristian Wider, Dennis W Dickson, A Jon Stoessl, et al.
Parkinsonism & Related Disorders|September 2, 2009
LINGO1 rs9652490 is associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Owen A Ross, Christian Wider, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.
Neurogenetics|April 7, 2010
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's diseaseJan O Aasly, Carles Vilariño-Güell, Justus C Dachsel, et al.
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.
Nature Genetics|January 13, 2009
DCTN1 mutations in Perry syndromeMatthew J Farrer, Mary M Hulihan, Jennifer M Kachergus, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Pageof 6