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K Fujieda

Showing results (11-20 of 135) with videos related to

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Indian Journal of Pediatrics|November 1, 1989
Advances in insulin therapy for insulin-dependent diabetic childrenN Matsuura, Y Mikami, K Fujieda
The Journal of Clinical Endocrinology and Metabolism|July 1, 1993
de novo mutation causes steroid 21-hydroxylase deficiency in one family of HLA-identical affected and unaffected siblingsT Tajima, K Fujieda, Y Fujii-Kuriyama
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 27, 2009
A novel mutation (V101A) of the LHX4 gene in a Japanese patient with combined pituitary hormone deficiencyT Tajima, T Yorifuji, K Ishizu, et al.
Neurologia Medico-Chirurgica|March 1, 1993
Endocrine functions in children with suprasellar germinomaT Aida, H Abe, K Fujieda, et al.
Journal of Human Genetics|March 18, 2000
A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversalK Okuhara, T Tajima, J Nakae, et al.
Clinical Cardiology|February 1, 1994
Decreased adrenergic response in hypertensive patients without left ventricular hypertrophyY Sugishita, K Iida, K Fujieda, et al.
Journal of Clinical Laboratory Analysis|September 25, 2012
Development of a bioassay system for human growth hormone determination with close correlation to immunoassayM Maimaiti, Y Tanahashi, Z Mohri, et al.
The Journal of Biological Chemistry|September 15, 1995
Replacements of leucine 87 in human insulin receptor alter affinity for insulinJ Nakae, H Morioka, E Ohtsuka, et al.
Human Molecular Genetics|July 1, 1994
A novel mutation localized in the 3' non-HMG box region of the SRY gene in 46,XY gonadal dysgenesisT Tajima, J Nakae, N Shinohara, et al.
Nihon Seirigaku Zasshi. Journal of the Physiological Society of Japan|September 1, 1974
[Proceedings: Rein control of ACTH]M Kaneko, S Wada, K Fujieda, et al.
Pageof 14

Showing results (11-20 of 135) with videos related to

Sort By:
Pageof 14
Indian Journal of Pediatrics|November 1, 1989
Advances in insulin therapy for insulin-dependent diabetic childrenN Matsuura, Y Mikami, K Fujieda
The Journal of Clinical Endocrinology and Metabolism|July 1, 1993
de novo mutation causes steroid 21-hydroxylase deficiency in one family of HLA-identical affected and unaffected siblingsT Tajima, K Fujieda, Y Fujii-Kuriyama
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 27, 2009
A novel mutation (V101A) of the LHX4 gene in a Japanese patient with combined pituitary hormone deficiencyT Tajima, T Yorifuji, K Ishizu, et al.
Neurologia Medico-Chirurgica|March 1, 1993
Endocrine functions in children with suprasellar germinomaT Aida, H Abe, K Fujieda, et al.
Journal of Human Genetics|March 18, 2000
A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversalK Okuhara, T Tajima, J Nakae, et al.
Clinical Cardiology|February 1, 1994
Decreased adrenergic response in hypertensive patients without left ventricular hypertrophyY Sugishita, K Iida, K Fujieda, et al.
Journal of Clinical Laboratory Analysis|September 25, 2012
Development of a bioassay system for human growth hormone determination with close correlation to immunoassayM Maimaiti, Y Tanahashi, Z Mohri, et al.
The Journal of Biological Chemistry|September 15, 1995
Replacements of leucine 87 in human insulin receptor alter affinity for insulinJ Nakae, H Morioka, E Ohtsuka, et al.
Human Molecular Genetics|July 1, 1994
A novel mutation localized in the 3' non-HMG box region of the SRY gene in 46,XY gonadal dysgenesisT Tajima, J Nakae, N Shinohara, et al.
Nihon Seirigaku Zasshi. Journal of the Physiological Society of Japan|September 1, 1974
[Proceedings: Rein control of ACTH]M Kaneko, S Wada, K Fujieda, et al.
Pageof 14