Art
J-GLOBAL ID:200902116011504965   Reference number:97A0728660

Follow-up Study of Seventy Cases with 21-Hydroxylase Deficiency Detected in Neonatal Period. Part 1. Clinical Findings before Treatment.

新生児期に発見された先天性副腎過形成症(21-水酸化酵素欠損)70例の追跡調査結果 第1編 治療開始前における臨床所見
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Material:
Volume: 101  Issue:Page: 1149-1157  Publication year: Jul. 1997 
JST Material Number: F0896A  ISSN: 0001-6543  CODEN: NIPOA  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Endocrine diseases 
Reference (24):
  • SUWA, S. Nationwide survey of neonatal-screening for congenital adrenal hyperplasia in Japan. Screening. 1994, 3, 141-151
  • PRADER, A. Der genitalbefund beim Pseudohermaphroditismus des femininums des kongenitalen adrenogenitalen Syndroms. Helv Paediatr Acta. 1954, 9, 231-248
  • 諏訪〓三. 先天性副腎皮質過形成症の実態調査結果 第四編 主症状の検討. 日児誌. 1982, 86, 2162-2167
  • 諏訪〓三. 先天性副腎皮質過形成症の障害に関するアンケート調査結果. 厚生省心身障害研究, マススクリーニングに関する研究, 昭和60年度研究報告書. 1986, 274-277
  • 諏訪〓三. 先天性副腎過形成のマススクリーニングの現状-性分化異常における意義を中心に-. ホと臨床. 1990, 38, 743-748
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