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Annals of Neurology
|
February 1, 1997
Maternal inheritance in Parkinson's disease
G F Wooten, L J Currie, J P Bennett, et al.
Parkinsonism & Related Disorders
|
March 15, 2001
Gender ratio differences between Parkinson's disease patients and their affected relatives
R H. Swerdlow, W D. Parker, L J. Currie, et al.
Archives of Neurology
|
February 15, 2001
Induction by dopamine D1 receptor agonist ABT-431 of dyskinesia similar to levodopa in patients with Parkinson disease
O Rascol, J G Nutt, O Blin, et al.
American Journal of Medical Genetics
|
April 27, 2002
Segregation analysis of Parkinson disease revealing evidence for a major causative gene
N E Maher, L J Currie, A M Lazzarini, et al.
Annals of Neurology
|
December 16, 1998
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family
R H Swerdlow, J K Parks, J N Davis, et al.
Neurology
|
September 26, 2001
Genome-wide scan for Parkinson's disease: the GenePD Study
A L DeStefano, L I Golbe, M H Mark, et al.
Neurology
|
January 10, 2002
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study
N E Maher, L I Golbe, A M Lazzarini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study
Samer Karamohamed, L I Golbe, M H Mark, et al.
Neurology
|
December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study
S Karamohamed, A L DeStefano, J B Wilk, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Annals of Neurology
|
February 1, 1997
Maternal inheritance in Parkinson's disease
G F Wooten, L J Currie, J P Bennett, et al.
Parkinsonism & Related Disorders
|
March 15, 2001
Gender ratio differences between Parkinson's disease patients and their affected relatives
R H. Swerdlow, W D. Parker, L J. Currie, et al.
Archives of Neurology
|
February 15, 2001
Induction by dopamine D1 receptor agonist ABT-431 of dyskinesia similar to levodopa in patients with Parkinson disease
O Rascol, J G Nutt, O Blin, et al.
American Journal of Medical Genetics
|
April 27, 2002
Segregation analysis of Parkinson disease revealing evidence for a major causative gene
N E Maher, L J Currie, A M Lazzarini, et al.
Annals of Neurology
|
December 16, 1998
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family
R H Swerdlow, J K Parks, J N Davis, et al.
Neurology
|
September 26, 2001
Genome-wide scan for Parkinson's disease: the GenePD Study
A L DeStefano, L I Golbe, M H Mark, et al.
Neurology
|
January 10, 2002
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study
N E Maher, L I Golbe, A M Lazzarini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study
Samer Karamohamed, L I Golbe, M H Mark, et al.
Neurology
|
December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study
S Karamohamed, A L DeStefano, J B Wilk, et al.
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of 2