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No to Hattatsu = Brain and Development
|
January 1, 1986
[Clinical and experimental studies of auditory brainstem responses in insulin-dependent diabetes mellitus]
K Oda, R Murata, G Isshiki, et al.
Ryoikibetsu Shokogun Shirizu
|
May 20, 1998
[Disorders of tetrahydrobiopterin homeostasis]
H Shintaku, M Asada, G Isshiki, et al.
Horumon to Rinsho. Clinical Endocrinology
|
June 1, 1983
[Pituitary dwarfism that showed Perthes-like symptoms during thyroid hormone administration]
K Fujita, S Minamino, H Aoki, et al.
Clinical Chemistry
|
June 6, 2000
Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate reader
A Fujimoto, Y Okano, T Miyagi, et al.
Journal of Human Genetics
|
May 13, 1999
Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients
T Imamura, Y Okano, H Shintaku, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
June 13, 2001
Mass screening of galactosemia: improved Beutler Test using automated quantitative fluorescence assay
A Fujimoto, Y Okano, T Miyagi, et al.
The Tohoku Journal of Experimental Medicine
|
April 1, 1976
Prenatal diagnosis and fetal pathology of Tay-Sachs disease
S Higami, K Nishizawa, K Omura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1983
Immunofluorescence staining and immunological studies of arylsulphatase A of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts
A Tanaka, S Higami, G Isshiki, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
Normal pterin values in urine and serum in neonates and its age-related change throughout life
H Shintaku, G Isshiki, Y Hase, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Molecular genetics of Tay-Sachs disease in Japan
A Tanaka, H Sakazaki, H Murakami, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 96) with videos related to
Sort By:
Page
of 10
No to Hattatsu = Brain and Development
|
January 1, 1986
[Clinical and experimental studies of auditory brainstem responses in insulin-dependent diabetes mellitus]
K Oda, R Murata, G Isshiki, et al.
Ryoikibetsu Shokogun Shirizu
|
May 20, 1998
[Disorders of tetrahydrobiopterin homeostasis]
H Shintaku, M Asada, G Isshiki, et al.
Horumon to Rinsho. Clinical Endocrinology
|
June 1, 1983
[Pituitary dwarfism that showed Perthes-like symptoms during thyroid hormone administration]
K Fujita, S Minamino, H Aoki, et al.
Clinical Chemistry
|
June 6, 2000
Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate reader
A Fujimoto, Y Okano, T Miyagi, et al.
Journal of Human Genetics
|
May 13, 1999
Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients
T Imamura, Y Okano, H Shintaku, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
June 13, 2001
Mass screening of galactosemia: improved Beutler Test using automated quantitative fluorescence assay
A Fujimoto, Y Okano, T Miyagi, et al.
The Tohoku Journal of Experimental Medicine
|
April 1, 1976
Prenatal diagnosis and fetal pathology of Tay-Sachs disease
S Higami, K Nishizawa, K Omura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1983
Immunofluorescence staining and immunological studies of arylsulphatase A of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts
A Tanaka, S Higami, G Isshiki, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
Normal pterin values in urine and serum in neonates and its age-related change throughout life
H Shintaku, G Isshiki, Y Hase, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Molecular genetics of Tay-Sachs disease in Japan
A Tanaka, H Sakazaki, H Murakami, et al.
Page
of 10