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Molecular Psychiatry|April 20, 2004
Association in Japanese patients between neuroleptic malignant syndrome and functional polymorphisms of the dopamine D(2) receptor geneI Kishida, C Kawanishi, T Furuno, et al.Psychiatry and Clinical Neurosciences|April 4, 2001
No evidence of an association between CYP2D6 polymorphisms among Japanese and dementia with Lewy bodiesT Furuno, C Kawanishi, E Iseki, et al.Molecular Pharmacology|May 9, 1998
Residues at the subunit interfaces of the nicotinic acetylcholine receptor that contribute to alpha-conotoxin M1 bindingN Sugiyama, P Marchot, C Kawanishi, et al.Brain & Development|March 1, 1996
Pelizaeus-Merzbacher-like disease: female case reportA Nezu, S Kimura, S Uehara, et al.Psychiatric Genetics|February 24, 2001
Lack of association in Japanese patients between neuroleptic malignant syndrome and a debrisoquine 4-hydroxylase genotype with low enzyme activityC Kawanishi, T Furuno, H Onishi, et al.Journal of the Neurological Sciences|November 6, 1998
Mutation involving cytochrome P450IID6 in two Japanese patients with neuroleptic malignant syndromeC Kawanishi, Y Shimoda, J Fujimaki, et al.Human Mutation|August 14, 1999
A novel missense mutation (G209R) in exon 8 of the presenilin 1 gene in a Japanese family with presenile familial Alzheimer's disease. Mutation in brief no. 254. OnlineN Sugiyama, K Suzuki, T Matsumura, et al.Neurology|January 1, 1997
Mutations in the proteolipid protein gene in Japanese families with Pelizaeus-Merzbacher diseaseK Inoue, H Osaka, C Kawanishi, et al.American Journal of Human Genetics|July 1, 1996
A duplicated PLP gene causing Pelizaeus-Merzbacher disease detected by comparative multiplex PCRK Inoue, H Osaka, N Sugiyama, et al.The American Journal of Psychiatry|September 12, 1998
Lack of association between neuroleptic malignant syndrome and polymorphisms in the 5-HT1A and 5-HT2A receptor genesC Kawanishi, T Hanihara, Y Shimoda, et al.Pageof 3