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Annals of Human Genetics
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March 30, 2000
Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany
C Klein, P Vieregge, J Hagenah, et al.
Nature Genetics
|
December 1, 1993
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q
T G Nygaard, K C Wilhelmsen, N J Risch, et al.
Annals of Neurology
|
November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation
S B Bressman, D de Leon, P L Kramer, et al.
American Journal of Human Genetics
|
March 1, 1990
Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance
N J Risch, S B Bressman, D deLeon, et al.
Neurology
|
January 24, 2002
Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence
R Saunders-Pullman, J Shriberg, G Heiman, et al.
Neurology
|
May 10, 2000
The DYT1 phenotype and guidelines for diagnostic testing
S B Bressman, C Sabatti, D Raymond, et al.
Neurology
|
June 1, 1997
Secondary dystonia and the DYTI gene
S B Bressman, D de Leon, D Raymond, et al.
Nature Genetics
|
June 1, 1994
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
E H Corder, A M Saunders, N J Risch, et al.
Human Molecular Genetics
|
June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia
C Klein, M F Brin, D de Leon, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 2007
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus
G C DeLuca, S V Ramagopalan, B M Herrera, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Annals of Human Genetics
|
March 30, 2000
Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany
C Klein, P Vieregge, J Hagenah, et al.
Nature Genetics
|
December 1, 1993
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q
T G Nygaard, K C Wilhelmsen, N J Risch, et al.
Annals of Neurology
|
November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation
S B Bressman, D de Leon, P L Kramer, et al.
American Journal of Human Genetics
|
March 1, 1990
Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance
N J Risch, S B Bressman, D deLeon, et al.
Neurology
|
January 24, 2002
Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence
R Saunders-Pullman, J Shriberg, G Heiman, et al.
Neurology
|
May 10, 2000
The DYT1 phenotype and guidelines for diagnostic testing
S B Bressman, C Sabatti, D Raymond, et al.
Neurology
|
June 1, 1997
Secondary dystonia and the DYTI gene
S B Bressman, D de Leon, D Raymond, et al.
Nature Genetics
|
June 1, 1994
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
E H Corder, A M Saunders, N J Risch, et al.
Human Molecular Genetics
|
June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia
C Klein, M F Brin, D de Leon, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 2007
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus
G C DeLuca, S V Ramagopalan, B M Herrera, et al.
Page
of 4