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G Takada

Showing results (171-180 of 201) with videos related to

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Human Genetics|June 1, 1994
Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemiaK Nanao, K Okamura-Ikeda, Y Motokawa, et al.
Sleep Medicine|July 5, 2001
Hypersomnia due to acute disseminated encephalomyelitis in a 5-year-old girlT Kanbayashi, A Goto, Y Hishikawa, et al.
Human Pathology|March 1, 1997
Heterogeneity of liver disorder in type B Niemann-Pick diseaseT Takahashi, K Akiyama, M Tomihara, et al.
Immunology|September 1, 1996
Cytotoxic activity against tumour cells mediated by intermediate TCR cells in the liver and spleenT Kawamura, Y Kawachi, T Moroda, et al.
Journal of the Neurological Sciences|December 1, 1995
Congenital hypomyelination neuropathy: decreased expression of the P2 protein in peripheral nerve with normal DNA sequence of the coding regionY Sawaishi, K Hayasaka, A Goto, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Acid sphingomyelinase deficiency: cardiac dysfunction and characteristic findings of the coronary arteriesH Ishii, T Takahashi, M Toyono, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
3-Methylglutaconic aciduria type I: clinical heterogeneity as a neurometabolic diseaseY Shoji, T Takahashi, Y Sawaishi, et al.
Genomics|September 1, 1993
Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ)K Hayasaka, M Himoro, Y Wang, et al.
The Tohoku Journal of Experimental Medicine|October 1, 1995
Identification and expression of a missense mutation (Y446C) in the acid sphingomyelinase gene from a Japanese patient with type A Niemann-Pick diseaseT Takahashi, M Suchi, W Sato, et al.
Biochemistry and Molecular Biology International|September 1, 1993
New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1M Himoro, H Yoshikawa, T Matsui, et al.
Pageof 21

Showing results (171-180 of 201) with videos related to

Sort By:
Pageof 21
Human Genetics|June 1, 1994
Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemiaK Nanao, K Okamura-Ikeda, Y Motokawa, et al.
Sleep Medicine|July 5, 2001
Hypersomnia due to acute disseminated encephalomyelitis in a 5-year-old girlT Kanbayashi, A Goto, Y Hishikawa, et al.
Human Pathology|March 1, 1997
Heterogeneity of liver disorder in type B Niemann-Pick diseaseT Takahashi, K Akiyama, M Tomihara, et al.
Immunology|September 1, 1996
Cytotoxic activity against tumour cells mediated by intermediate TCR cells in the liver and spleenT Kawamura, Y Kawachi, T Moroda, et al.
Journal of the Neurological Sciences|December 1, 1995
Congenital hypomyelination neuropathy: decreased expression of the P2 protein in peripheral nerve with normal DNA sequence of the coding regionY Sawaishi, K Hayasaka, A Goto, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Acid sphingomyelinase deficiency: cardiac dysfunction and characteristic findings of the coronary arteriesH Ishii, T Takahashi, M Toyono, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
3-Methylglutaconic aciduria type I: clinical heterogeneity as a neurometabolic diseaseY Shoji, T Takahashi, Y Sawaishi, et al.
Genomics|September 1, 1993
Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ)K Hayasaka, M Himoro, Y Wang, et al.
The Tohoku Journal of Experimental Medicine|October 1, 1995
Identification and expression of a missense mutation (Y446C) in the acid sphingomyelinase gene from a Japanese patient with type A Niemann-Pick diseaseT Takahashi, M Suchi, W Sato, et al.
Biochemistry and Molecular Biology International|September 1, 1993
New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1M Himoro, H Yoshikawa, T Matsui, et al.
Pageof 21