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Horumon to Rinsho. Clinical Endocrinology
|
January 1, 1982
[Cretinism mass-screening study by solid phase TSH-RIA method (author's transl)]
Y Okano, Y Osasa, Y Hase, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Short tandem repeat polymorphisms in Japanese families with phenylketonuria
Y Kang, Y Okano, Y Hase, et al.
Keisei Geka. Plastic & Reconstructive Surgery
|
March 1, 1972
[Experience and problems in nasal reconstruction]
T Oura, J Hamamoto, A Ariga, et al.
Human Genetics
|
March 12, 1976
47,+(9q-) in unrelated three children with plasma growth hormone deficiency
H Fujita, M Shimazaki, T Takeuchi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Effects of phenylalanine loading on protein synthesis in the fetal heart and brain of rat: an experimental approach to maternal phenylketonuria
Y Okano, I Z Chow, G Isshiki, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1993
Experimental research on a fetal treatment for tetrahydrobiopterin deficiency
H Shintaku, T Nakajima, T Imamura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
A case of tetrahydrobiopterin deficiency due to a defective synthesis of dihydrobiopterin
Y Hase, H Shintaku, T Turuhara, et al.
Lancet (London, England)
|
September 29, 1979
Fetal heart-rate in congenital hypothyroidism
K Miyai, H Mizuta, N Amino, et al.
Diabetes, Obesity & Metabolism
|
July 17, 2015
Efficacy and safety of once-weekly dulaglutide in combination with sulphonylurea and/or biguanide compared with once-daily insulin glargine in Japanese patients with type 2 diabetes: a randomized, open-label, phase III, non-inferiority study
E Araki, N Inagaki, Y Tanizawa, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 1, 1985
Zinc status of untreated histidinemic children
A Kitano, A Higashi, N Nagata, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 76) with videos related to
Sort By:
Page
of 8
Horumon to Rinsho. Clinical Endocrinology
|
January 1, 1982
[Cretinism mass-screening study by solid phase TSH-RIA method (author's transl)]
Y Okano, Y Osasa, Y Hase, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Short tandem repeat polymorphisms in Japanese families with phenylketonuria
Y Kang, Y Okano, Y Hase, et al.
Keisei Geka. Plastic & Reconstructive Surgery
|
March 1, 1972
[Experience and problems in nasal reconstruction]
T Oura, J Hamamoto, A Ariga, et al.
Human Genetics
|
March 12, 1976
47,+(9q-) in unrelated three children with plasma growth hormone deficiency
H Fujita, M Shimazaki, T Takeuchi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Effects of phenylalanine loading on protein synthesis in the fetal heart and brain of rat: an experimental approach to maternal phenylketonuria
Y Okano, I Z Chow, G Isshiki, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1993
Experimental research on a fetal treatment for tetrahydrobiopterin deficiency
H Shintaku, T Nakajima, T Imamura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
A case of tetrahydrobiopterin deficiency due to a defective synthesis of dihydrobiopterin
Y Hase, H Shintaku, T Turuhara, et al.
Lancet (London, England)
|
September 29, 1979
Fetal heart-rate in congenital hypothyroidism
K Miyai, H Mizuta, N Amino, et al.
Diabetes, Obesity & Metabolism
|
July 17, 2015
Efficacy and safety of once-weekly dulaglutide in combination with sulphonylurea and/or biguanide compared with once-daily insulin glargine in Japanese patients with type 2 diabetes: a randomized, open-label, phase III, non-inferiority study
E Araki, N Inagaki, Y Tanizawa, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 1, 1985
Zinc status of untreated histidinemic children
A Kitano, A Higashi, N Nagata, et al.
Page
of 8