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European Journal of Neurology
|
December 18, 2008
R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family
F Sina, S Shojaee, E Elahi, et al.
Clinical Genetics
|
April 25, 2017
A novel TRPA1 variant is associated with carbamazepine-responsive cramp-fasciculation syndrome
M J Nirenberg, R Chaouni, T M Biller, et al.
Clinical Genetics
|
January 3, 2013
Rapid disease progression in adult-onset mitochondrial membrane protein-associated neurodegeneration
O Dogu, C E Krebs, H Kaleagasi, et al.
Neuroscience Letters
|
October 19, 2004
Mitochondrial polymporphisms in Parkinson's Disease
D Otaegui, C Paisán, A Sáenz, et al.
Neurobiology of Aging
|
April 5, 2008
Whole genome analysis in a consanguineous family with early onset Alzheimer's disease
J Clarimón, R Djaldetti, A Lleó, et al.
Neuroscience Letters
|
August 15, 2006
Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease
L Blázquez, D Otaegui, A Sáenz, et al.
Journal of Neurology
|
October 1, 2014
Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia
A Deik, B Johannes, J C Rucker, et al.
Neurology
|
September 15, 2005
LRRK2 gene in Parkinson disease: mutation analysis and case control association study
C Paisán-Ruíz, A E Lang, T Kawarai, et al.
Journal of Medical Genetics
|
February 10, 2006
Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium
C Paisán-Ruíz, E W Evans, S Jain, et al.
Brain : a Journal of Neurology
|
February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene
A Sáenz, F Leturcq, A M Cobo, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
European Journal of Neurology
|
December 18, 2008
R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family
F Sina, S Shojaee, E Elahi, et al.
Clinical Genetics
|
April 25, 2017
A novel TRPA1 variant is associated with carbamazepine-responsive cramp-fasciculation syndrome
M J Nirenberg, R Chaouni, T M Biller, et al.
Clinical Genetics
|
January 3, 2013
Rapid disease progression in adult-onset mitochondrial membrane protein-associated neurodegeneration
O Dogu, C E Krebs, H Kaleagasi, et al.
Neuroscience Letters
|
October 19, 2004
Mitochondrial polymporphisms in Parkinson's Disease
D Otaegui, C Paisán, A Sáenz, et al.
Neurobiology of Aging
|
April 5, 2008
Whole genome analysis in a consanguineous family with early onset Alzheimer's disease
J Clarimón, R Djaldetti, A Lleó, et al.
Neuroscience Letters
|
August 15, 2006
Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease
L Blázquez, D Otaegui, A Sáenz, et al.
Journal of Neurology
|
October 1, 2014
Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia
A Deik, B Johannes, J C Rucker, et al.
Neurology
|
September 15, 2005
LRRK2 gene in Parkinson disease: mutation analysis and case control association study
C Paisán-Ruíz, A E Lang, T Kawarai, et al.
Journal of Medical Genetics
|
February 10, 2006
Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium
C Paisán-Ruíz, E W Evans, S Jain, et al.
Brain : a Journal of Neurology
|
February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene
A Sáenz, F Leturcq, A M Cobo, et al.
Page
of 1