Motomura K | Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences

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概要

• 同名の論文著者
• Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciencesの論文著者

関連著者

• Motomura K

  Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences

• Kinoshita E

  Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences

• Kinoshita E

  Department Of Pediatrics Nagasaki University School Of Medicine

• Shimizu T

  Department Of Applied Chemistry Faculty Of Engineering Utsunomiya University

• Shimizu T

  Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences

• Yoshimoto M

  Children's Clinic Yoshimoto

• Yoshimoto M

  Children's Clinic Yoshimoto

• Baba T

  Baba Children's Clinic

• Hirota T

  Children's Clinic Hirota

• Baba T

  Baba Children's Clinic

• Hirota T

  Department Of Legal Medicine Nara Medical University

• Kawaguchi T

  Department Of Applied Life Sciences Graduate School Of Life And Environmental Sciences Osaka Prefect

• Kawaguchi T

  Department Of Pediatrics Nagasaki University School Of Medicine

• Hara M

  Department Of Anatomy St. Marianna University School Of Medicine

• Oka S

  Sasebo Kyosai Hospital

• Hirota T

  Children's Clinic Hirota

• Dateki S

  Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences

• Dateki S

  Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences

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著作論文

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

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