Kinoshita E | Department Of Pediatrics Nagasaki University School Of Medicine

スポンサーリンク

概要

関連著者

もっと見る

著作論文

243 A CASE OF McCUNE-ALBRIGHT SYNDROME WITH NARROWING OPTIC CANAL : A TRIAL OF INTRAVENOUS PAMIDRONATE TREATMENT
Mental Retardation in a Boy with Congenital Adrenal Hypoplasia : A Clue to Contiguous Gene Syndrome Involving DAX1 and IL1RAPL
168 A frameshift mutation and a familial deletion mutation of the DAX1 gene in patients with X-linked adrenal hypoplasia congenita
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"

スポンサーリンク