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Neurology
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March 1, 1987
Dihydrobiopterin synthesis defect: an adult with diurnal fluctuation of symptoms
K Tanaka, M Yoneda, T Nakajima, et al.
Journal of Neurochemistry
|
February 1, 1979
Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency
Y Eto, M Owada, T Kitagawa, et al.
Biochemical and Biophysical Research Communications
|
June 15, 1983
Bone marrow transplantation for Niemann-Pick mice
T Sakiyama, M Tsuda, M Owada, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1980
Analysis of RNA specific for the transforming agent of R-strain avian erythroblastosis virus
K Toyoshima, T Kamahora, H Sugiyama, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Subcellular localization of acid sphingomyelinase and lipid in Niemann-Pick mice
T Sakiyama, K Akashi, A Akatsuka, et al.
Internal Medicine (Tokyo, Japan)
|
April 13, 2001
Successful steroid therapy for cefdinir-induced acute tubulointerstitial nephritis with progressive renal failure
Y Kimura, M Kawamura, M Owada, et al.
American Journal of Human Genetics
|
September 1, 1990
Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene
S Kajihara, T Mukai, Y Arai, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis
T Matsuura, R Hoshide, M Fukushima, et al.
Acta Paediatrica Japonica : Overseas Edition
|
August 1, 1988
Dietary treatment of PKU using a low-phenylalanine peptide milk
M Owada, M Abe, M Tanimoto, et al.
The Tohoku Journal of Experimental Medicine
|
March 30, 2000
Risk factors and triggers of sudden death in the working generation: an autopsy proven case-control study
M Owada, Y Aizawa, K Kurihara, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 119) with videos related to
Sort By:
Page
of 12
Neurology
|
March 1, 1987
Dihydrobiopterin synthesis defect: an adult with diurnal fluctuation of symptoms
K Tanaka, M Yoneda, T Nakajima, et al.
Journal of Neurochemistry
|
February 1, 1979
Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency
Y Eto, M Owada, T Kitagawa, et al.
Biochemical and Biophysical Research Communications
|
June 15, 1983
Bone marrow transplantation for Niemann-Pick mice
T Sakiyama, M Tsuda, M Owada, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1980
Analysis of RNA specific for the transforming agent of R-strain avian erythroblastosis virus
K Toyoshima, T Kamahora, H Sugiyama, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Subcellular localization of acid sphingomyelinase and lipid in Niemann-Pick mice
T Sakiyama, K Akashi, A Akatsuka, et al.
Internal Medicine (Tokyo, Japan)
|
April 13, 2001
Successful steroid therapy for cefdinir-induced acute tubulointerstitial nephritis with progressive renal failure
Y Kimura, M Kawamura, M Owada, et al.
American Journal of Human Genetics
|
September 1, 1990
Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene
S Kajihara, T Mukai, Y Arai, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis
T Matsuura, R Hoshide, M Fukushima, et al.
Acta Paediatrica Japonica : Overseas Edition
|
August 1, 1988
Dietary treatment of PKU using a low-phenylalanine peptide milk
M Owada, M Abe, M Tanimoto, et al.
The Tohoku Journal of Experimental Medicine
|
March 30, 2000
Risk factors and triggers of sudden death in the working generation: an autopsy proven case-control study
M Owada, Y Aizawa, K Kurihara, et al.
Page
of 12