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Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1990
Fall and rise variations of serum GGTP in preoperative infants with biliary atresia
Y Tazawa, M Nakagawa, D Abukawa, et al.
Acta Neurologica Scandinavica
|
November 1, 1991
Study of cytoskeletal proteins in fibroblasts cultured from familial Alzheimer's disease
M Takeda, T Nishimura, S Hariguchi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Cloning of a defective gene encoding the pyruvate dehydrogenase E1 alpha subunit from a patient with its deficiency
H Endo, S Miyabayashi, K Hasegawa, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms
|
January 5, 2000
Region between alpha-helices 3 and 4 of the mad homology 2 domain of Smad4: functional roles in oligomer formation and transcriptional activation
K Tada, H Inoue, T Ebisawa, et al.
International Journal of Oral and Maxillofacial Surgery
|
June 1, 1989
Granular cell ameloblastoma. A rare variant
G Yamamoto, K Yoshitake, K Tada, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
June 1, 1984
Fecal and biliary bile acid patterns in children with bile acid malabsorption
Y Tazawa, M Yamada, M Nakagawa, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
June 1, 1984
Familial intrahepatic cholestasis associated with progressive neuromuscular disease and vitamin E deficiency
M Nakagawa, Y Tazawa, Y Kobayashi, et al.
The British Journal of Ophthalmology
|
October 20, 2010
Evaluation of histamine-induced conjunctival oedema in guinea pigs by means of image analysis
A Takahashi, T Sumi, K Tada, et al.
The Tohoku Journal of Experimental Medicine
|
January 1, 1985
Postheparin plasma lipoprotein lipase activity in heterozygotes of familial lipoprotein lipase deficiency
Y Kondo, I Kurobane, K Omura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
A survey on prenatal diagnosis of inherited metabolic diseases in Japan
K Tada, J Aikawa, Y Igarashi, et al.
Page
of 63
Search research articles
Search
Showing results (421-430 of 623) with videos related to
Sort By:
Page
of 63
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1990
Fall and rise variations of serum GGTP in preoperative infants with biliary atresia
Y Tazawa, M Nakagawa, D Abukawa, et al.
Acta Neurologica Scandinavica
|
November 1, 1991
Study of cytoskeletal proteins in fibroblasts cultured from familial Alzheimer's disease
M Takeda, T Nishimura, S Hariguchi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Cloning of a defective gene encoding the pyruvate dehydrogenase E1 alpha subunit from a patient with its deficiency
H Endo, S Miyabayashi, K Hasegawa, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms
|
January 5, 2000
Region between alpha-helices 3 and 4 of the mad homology 2 domain of Smad4: functional roles in oligomer formation and transcriptional activation
K Tada, H Inoue, T Ebisawa, et al.
International Journal of Oral and Maxillofacial Surgery
|
June 1, 1989
Granular cell ameloblastoma. A rare variant
G Yamamoto, K Yoshitake, K Tada, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
June 1, 1984
Fecal and biliary bile acid patterns in children with bile acid malabsorption
Y Tazawa, M Yamada, M Nakagawa, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
June 1, 1984
Familial intrahepatic cholestasis associated with progressive neuromuscular disease and vitamin E deficiency
M Nakagawa, Y Tazawa, Y Kobayashi, et al.
The British Journal of Ophthalmology
|
October 20, 2010
Evaluation of histamine-induced conjunctival oedema in guinea pigs by means of image analysis
A Takahashi, T Sumi, K Tada, et al.
The Tohoku Journal of Experimental Medicine
|
January 1, 1985
Postheparin plasma lipoprotein lipase activity in heterozygotes of familial lipoprotein lipase deficiency
Y Kondo, I Kurobane, K Omura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
A survey on prenatal diagnosis of inherited metabolic diseases in Japan
K Tada, J Aikawa, Y Igarashi, et al.
Page
of 63