Search Results1-3 of  3

  • Maesaka Hatae ID: 9000003461712

    Odawara Health and Welfare Center (2003 from CiNii)

    Articles in CiNii:36

    • Pathogenesis of central sexual precocity. (1995)
    • Clinical characteristics of 13 cases diagnosed as nonclassical 3β-hydroxysteroid dehydrogenase deficiency. (1996)
    • Hypoparathyroidism caused by chromosome 22 q 11.2 microdeletion in children. (1997)
  • SUWA Seizo ID: 9000399769239

    Kanagawa Prefecture Medical Association -Inborn Error of Metabolism Task Committee- (2004 from CiNii)

    Articles in CiNii:117

    • A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17α-Hydroxylase/17m,20-Lyase Deficiency, but without Obvious CYP17 Gene Mutations (1999)
    • 日本の小児科の研究水準- 問題点と解決に向けて- (1996)
    • Eight Cases of Central Hypothyroidism Detected by Mass-screening for Congenital Hypothyroidism Using Simultaneous Measurement of TSH and T4 or ft4 (2000)
  • Suwa Seizo ID: 9000021843463

    Department of Endocrinology and Metabolism, Kanagawa Childen's Medical Center (1994 from CiNii)

    Articles in CiNii:1

    • Serum Levels of Intact Molecular Osteocalcin in Children with Growth Hormone (GH) Deficiency during GH Therapy : An Early Predictor of GH Therapy (1994)
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