Showing 1 - 20 results of 24 for search 'Bulman, D', query time: 0.04s
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1
Leninism and local interests: how cities in China benefit from concurrent leadership appointments by Jaros, K, Bulman, D
Published 2019Journal article -
2
THE GEOGRAPHY OF MS REFLECTS GENETIC SUSCEPTIBILITY by Ebers, G, Bulman, D
Published 1986Journal article -
3
Allele frequencies of the third component of complement (C3) in MS patients. by Bulman, D, Armstrong, H, Ebers, G
Published 1991Journal article -
4
The skeletal muscle sodium and chloride channel diseases. by Hudson, A, Ebers, G, Bulman, D
Published 1995Journal article -
5
Age of onset in siblings concordant for multiple sclerosis. by Bulman, D, Sadovnick, A, Ebers, G
Published 1991Journal article -
6
Parent-child concordance in multiple sclerosis. by Sadovnick, A, Bulman, D, Ebers, G
Published 1991Journal article -
7
A COMPARISON OF FAMILIAL AND SPORADIC MS by Weinshenker, B, Armstrong, H, Bulman, D, Ebers, G
Published 1986Journal article -
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A comparison of sporadic and familial multiple sclerosis. by Weinshenker, BG, Bulman, D, Carriere, W, Baskerville, J, Ebers, G
Published 1990Journal article -
9
MAPPING THE GENE FOR ACETAZOLAMIDE-RESPONSIVE HEREDITARY PAROXYSMAL CEREBELLAR-ATAXIA TO CHROMOSOME-19P by Bulman, D, Vonbrederlow, B, Hahn, A, Koopman, W, Ebers, G
Published 1995Journal article -
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Absence of antibody to HTLV I and III in sera of Canadian patients with multiple sclerosis and chronic myelopathy. by Rice, G, Armstrong, H, Bulman, D, Paty, D, Ebers, G
Published 1986Journal article -
12
Evidence favoring genetic heterogeneity for febrile convulsions. by Racacho, L, McLachlan, R, Ebers, G, Maher, J, Bulman, D
Published 2000Journal article -
13
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p. by von Brederlow, B, Hahn, A, Koopman, W, Ebers, G, Bulman, D
Published 1995Journal article -
14
The influence of gender on the susceptibility to multiple sclerosis in sibships. by Sadovnick, A, Bulman, D, Hashimoto, L, D'Hooghe, M, Ebers, G
Published 1991Journal article -
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A novel sodium channel mutation in a family with hypokalemic periodic paralysis. by Bulman, D, Scoggan, K, Oene, v, Nicolle, M, Hahn, A, Tollar, L, Ebers, G
Published 1999Journal article -
17
A population-based study of multiple sclerosis in twins. by Ebers, G, Bulman, D, Sadovnick, A, Paty, D, Warren, S, Hader, W, Murray, T, Seland, T, Duquette, P, Grey, T
Published 1986Journal article -
18
HYPOKALEMIC PERIODIC PARALYSIS IS LINKED TO THE ALPHA-1 SUBUNIT OF THE DIHYDROPYRIDINE-SENSITIVE CALCIUM-CHANNEL AT 1Q31-32 by Bulman, D, Tollar, L, Murray, J, Allon, M, Cousin, H, Crackower, M, Hudson, A, Ebers, G
Published 1994Journal article -
19
A population-based study of multiple sclerosis in twins: update. by Sadovnick, A, Armstrong, H, Rice, G, Bulman, D, Hashimoto, L, Paty, D, Hashimoto, SA, Warren, S, Hader, W, Murray, T
Published 1993Journal article -
20
A GENETIC-BASIS FOR FAMILIAL AGGREGATION IN MULTIPLE-SCLEROSIS by Ebers, G, Sadovnick, A, Risch, N, Bulman, D, Rice, G, Hashimoto, S, Paty, D, Oger, J, Metz, L, Bell, R, Warren, S, Hader, W, Auty, T, Nath, A, Gray, T, Oconnor, P, Nelson, R, Freedman, M, Brunet, D, Paulseth, R, Francis, G, Duquette, P, Murray, T, Bahn, V, Prysephillips, W
Published 1995Journal article