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Genes and Immunity
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July 26, 2002
A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis
E Akesson, A Oturai, J Berg, et al.
European Journal of Neurology
|
May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias
H F Harbo, J Finsterer, J Baets, et al.
European Journal of Neurology
|
May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders
J-M Burgunder, L Schöls, J Baets, et al.
Neurology
|
December 19, 2009
HLA-DRB1 and month of birth in multiple sclerosis
S V Ramagopalan, J Link, J K Byrnes, et al.
Genes and Immunity
|
December 24, 2010
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
I-L Mero, M Ban, Å R Lorentzen, et al.
European Journal of Neurology
|
January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias
T Gasser, J Finsterer, J Baets, et al.
European Journal of Neurology
|
December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disorders
J Finsterer, H F Harbo, J Baets, et al.
Molecular Psychiatry
|
January 29, 2014
Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci
O A Andreassen, H F Harbo, Y Wang, et al.
Tissue Antigens
|
March 3, 2004
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
H F Harbo, B A Lie, S Sawcer, et al.
Neurology
|
January 31, 2007
Familial effects on the clinical course of multiple sclerosis
A E Hensiek, S R Seaman, L F Barcellos, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Genes and Immunity
|
July 26, 2002
A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis
E Akesson, A Oturai, J Berg, et al.
European Journal of Neurology
|
May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias
H F Harbo, J Finsterer, J Baets, et al.
European Journal of Neurology
|
May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders
J-M Burgunder, L Schöls, J Baets, et al.
Neurology
|
December 19, 2009
HLA-DRB1 and month of birth in multiple sclerosis
S V Ramagopalan, J Link, J K Byrnes, et al.
Genes and Immunity
|
December 24, 2010
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
I-L Mero, M Ban, Å R Lorentzen, et al.
European Journal of Neurology
|
January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias
T Gasser, J Finsterer, J Baets, et al.
European Journal of Neurology
|
December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disorders
J Finsterer, H F Harbo, J Baets, et al.
Molecular Psychiatry
|
January 29, 2014
Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci
O A Andreassen, H F Harbo, Y Wang, et al.
Tissue Antigens
|
March 3, 2004
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
H F Harbo, B A Lie, S Sawcer, et al.
Neurology
|
January 31, 2007
Familial effects on the clinical course of multiple sclerosis
A E Hensiek, S R Seaman, L F Barcellos, et al.
Page
of 5