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Author Motomura, K: 9

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2002-12 101 A female case of classical 3β-hydroxysteroid dehydrogenase deficiency with multicystic ovary and anovulatory menstruation : Evaluation of ovarian function after puberty Shimizu, T; Motomura, K; Hirota, T; Kawaguchi, T; Kinoshita, E; Baba, T; Yoshimoto, M 508
2002-12 109 A case of allergy to gelatin included in the gonadotropin-releasing hormone analog "depot leuprorelin acetate" Kinoshita, E; Motomura, K; Shimizu, T; Yoshimoto, M 488
2003-12 243 A CASE OF McCUNE-ALBRIGHT SYNDROME WITH NARROWING OPTIC CANAL : A TRIAL OF INTRAVENOUS PAMIDRONATE TREATMENT Dateki, S; Motomura, K; Shimizu, T; Kinoshita, E 506
2003-12 40 A NOVEL MUTATION OF 25-HYDROXY VITAMIN D3 1α-HYDROXYLASE GENE IN A JAPANESE FAMILY WITH VITAMIN D DEPENDENT RICKETS TYPE1 Hara, M; Motomura, K; Shimizu, T; Kinoshita, E; Oka, S 486
2003-12 53 PITUITARY MAGNETIC RESONANCE IMAGING IN CHILDREN WITH GROWTH HORMONE DEFICIENCY Shimizu, T; Motomura, K; Kawaguchi, T; Kinoshita, E; Hirota, T; Baba, T; Yoshimoto, M 516
2002-12 64 GNAS1 mutation in a Japanese boy with progressive osseous heteroplasia. Motomura, K; Kinoshita, E; Shimizu, T; Yoshimoto, M 492
2003-12 66 Conventional detection of somatic GNAS1 mutation utilizing peripheral blood leukocyte in McCune-Albright syndrome Motomura, K; Kinoshita, E; Yoshimoto, M 491
2003-12 83 Analysis of suppressor of cytokine signaling-2 (SOCS-2) gene in overgrowth syndrome Motomura, K; Kinoshita, E 572
2002-12 98 A male-raised 46, XX case of congenital adrenal hyperplasia due to 21 hydroxylase deficiency Kinoshita, E; Motomura, K; Shimizu, T; Hirota, T; Baba, T; Yoshimoto, M 510

 

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