A Case of Congenital Hypopituitarism: Difficulty in the Diagnosis of ACTH Deficiency Due to High Serum Cortisol Levels from a Hypothyroid State

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Author(s)

    • NANAO Kenji
    • Endocrinology, Metabolism and Genetics Unit, Tokyo Metropolitan Kiyose Children's Hospital
    • MIYAMOTO Junko
    • Endocrinology, Metabolism and Genetics Unit, Tokyo Metropolitan Kiyose Children's Hospital
    • ANZO Makoto
    • Endocrinology, Metabolism and Genetics Unit, Tokyo Metropolitan Kiyose Children's Hospital
    • TSUKUDA Toshinori
    • Endocrinology, Metabolism and Genetics Unit, Tokyo Metropolitan Kiyose Children's Hospital
    • HASEGAWA Yukihiro
    • Endocrinology, Metabolism and Genetics Unit, Tokyo Metropolitan Kiyose Children's Hospital

Journal

  • Endocr J

    Endocr J 46(1), 183-186, 1999-02

References:  7

Cited by:  1

Codes

  • NII Article ID (NAID)
    10005241645
  • NII NACSIS-CAT ID (NCID)
    AA10901436
  • Text Lang
    ENG
  • Article Type
    Journal Article
  • ISSN
    09188959
  • Data Source
    CJP  CJPref 
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