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D A Dyment

Showing results (21-30 of 46) with videos related to

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Neurology|October 10, 2002
Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13S E Noble-Topham, D A Dyment, M Z Cader, et al.
European Journal of Neurology|December 9, 2009
Sex ratio of multiple sclerosis and clinical phenotypeS V Ramagopalan, J K Byrnes, S-M Orton, et al.
Clinical Genetics|October 9, 2016
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactylyK D Kernohan, A McBride, Y Xi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 28, 2009
Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative StudyS-M Orton, S V Ramagopalan, D Brocklebank, et al.
European Journal of Neurology|January 28, 2009
Age of puberty and the risk of multiple sclerosis: a population based studyS V Ramagopalan, W Valdar, M Criscuoli, et al.
Genes and Immunity|June 4, 2004
TCR beta polymorphisms and multiple sclerosisD A Dyment, J L Steckley, K Morrison, et al.
Neurology|June 10, 2009
Risk alleles for multiple sclerosis in multiplex familiesM J D'Netto, H Ward, K M Morrison, et al.
Neurogenetics|December 17, 2017
A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsyJ L Zambonin, D A Dyment, Y Xi, et al.
Neurology|January 7, 2011
MHC transmission: insights into gender bias in MS susceptibilityM J Chao, S V Ramagopalan, B M Herrera, et al.
European Journal of Medical Genetics|April 6, 2017
Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndromeP Y B Au, L Huang, S Broley, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Neurology|October 10, 2002
Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13S E Noble-Topham, D A Dyment, M Z Cader, et al.
European Journal of Neurology|December 9, 2009
Sex ratio of multiple sclerosis and clinical phenotypeS V Ramagopalan, J K Byrnes, S-M Orton, et al.
Clinical Genetics|October 9, 2016
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactylyK D Kernohan, A McBride, Y Xi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 28, 2009
Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative StudyS-M Orton, S V Ramagopalan, D Brocklebank, et al.
European Journal of Neurology|January 28, 2009
Age of puberty and the risk of multiple sclerosis: a population based studyS V Ramagopalan, W Valdar, M Criscuoli, et al.
Genes and Immunity|June 4, 2004
TCR beta polymorphisms and multiple sclerosisD A Dyment, J L Steckley, K Morrison, et al.
Neurology|June 10, 2009
Risk alleles for multiple sclerosis in multiplex familiesM J D'Netto, H Ward, K M Morrison, et al.
Neurogenetics|December 17, 2017
A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsyJ L Zambonin, D A Dyment, Y Xi, et al.
Neurology|January 7, 2011
MHC transmission: insights into gender bias in MS susceptibilityM J Chao, S V Ramagopalan, B M Herrera, et al.
European Journal of Medical Genetics|April 6, 2017
Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndromeP Y B Au, L Huang, S Broley, et al.
Pageof 5