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The Tohoku Journal of Experimental Medicine
|
April 1, 1974
Decrease of urinary acid mucopolysaccharides in Hurler's syndrome after plasma infusion
T Orii, M Yamaguchi, R Minami, et al.
Pediatrics
|
November 1, 1977
Hurler's syndromes without alpha-L-iduronidase deficiency
T Orii, K Sukegawa, R Minami, et al.
The Tohoku Journal of Experimental Medicine
|
March 1, 1987
A case of glutaric aciduria type I with unique abnormalities in the cerebral CT findings
S Yamaguchi, T Orii, K Yasuda, et al.
Transplantation Proceedings
|
December 20, 2000
Living-related liver transplantation in patients with pulmonary vascular disease
H Kikuchi, N Ohkohchi, T Orii, et al.
Journal of Clinical Immunology
|
May 1, 1992
Accelerated expression of secreted alpha-chain gene in anaphylactoid purpura
N Kondo, K Kasahara, S Shinoda, et al.
Human Mutation
|
January 1, 1995
Molecular basis of beta-ketothiolase deficiency: mutations and polymorphisms in the human mitochondrial acetoacetyl-coenzyme A thiolase gene
T Fukao, S Yamaguchi, T Orii, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1976
Three cases of GM1-gangliosidosis
T Kudoh, T Orii, T Nakao, et al.
The Journal of Rheumatology
|
July 1, 1989
B cell suppressing and CD8+ T cell enhancing effects of photosensitive dye platonin in humans
N Kondo, H Ko, F Motoyoshi, et al.
Pediatric Research
|
August 1, 1989
Major peroxisomal membrane polypeptides are synthesized in cultured skin fibroblasts from patients with Zellweger syndrome
Y Suzuki, N Shimozawa, T Orii, et al.
Ryoikibetsu Shokogun Shirizu
|
June 30, 1998
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]
K Sukegawa, S Tomatsu, N Kondo, et al.
Page
of 40
Search research articles
Search
Showing results (61-70 of 397) with videos related to
Sort By:
Page
of 40
The Tohoku Journal of Experimental Medicine
|
April 1, 1974
Decrease of urinary acid mucopolysaccharides in Hurler's syndrome after plasma infusion
T Orii, M Yamaguchi, R Minami, et al.
Pediatrics
|
November 1, 1977
Hurler's syndromes without alpha-L-iduronidase deficiency
T Orii, K Sukegawa, R Minami, et al.
The Tohoku Journal of Experimental Medicine
|
March 1, 1987
A case of glutaric aciduria type I with unique abnormalities in the cerebral CT findings
S Yamaguchi, T Orii, K Yasuda, et al.
Transplantation Proceedings
|
December 20, 2000
Living-related liver transplantation in patients with pulmonary vascular disease
H Kikuchi, N Ohkohchi, T Orii, et al.
Journal of Clinical Immunology
|
May 1, 1992
Accelerated expression of secreted alpha-chain gene in anaphylactoid purpura
N Kondo, K Kasahara, S Shinoda, et al.
Human Mutation
|
January 1, 1995
Molecular basis of beta-ketothiolase deficiency: mutations and polymorphisms in the human mitochondrial acetoacetyl-coenzyme A thiolase gene
T Fukao, S Yamaguchi, T Orii, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1976
Three cases of GM1-gangliosidosis
T Kudoh, T Orii, T Nakao, et al.
The Journal of Rheumatology
|
July 1, 1989
B cell suppressing and CD8+ T cell enhancing effects of photosensitive dye platonin in humans
N Kondo, H Ko, F Motoyoshi, et al.
Pediatric Research
|
August 1, 1989
Major peroxisomal membrane polypeptides are synthesized in cultured skin fibroblasts from patients with Zellweger syndrome
Y Suzuki, N Shimozawa, T Orii, et al.
Ryoikibetsu Shokogun Shirizu
|
June 30, 1998
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]
K Sukegawa, S Tomatsu, N Kondo, et al.
Page
of 40