Extensive clinical-experience - Nonclassical 21-hydroxylase deficiency (vol 91, pg 4205, 2006)

被引：0
|
作者：
New, Maria
机构：
来源：
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2007年 / 92卷 / 01期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：142 / 142
页数：1
相关论文
共 50 条
  • [1] Extensive clinical experience - Nonclassical 21-hydroxylase deficiency
    New, Maria I.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (11): : 4205 - 4214
  • [2] Clinical analysis of 78 patients with nonclassical 21-hydroxylase deficiency
    Liu, En
    Luo, Hengcong
    Zhou, Kailv
    Zhang, Ying
    ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2023, 308 (03) : 871 - 882
  • [3] Clinical analysis of 78 patients with nonclassical 21-hydroxylase deficiency
    En Liu
    Hengcong Luo
    Kailv Zhou
    Ying Zhang
    Archives of Gynecology and Obstetrics, 2023, 308 : 871 - 882
  • [4] Adult height of subjects with nonclassical 21-hydroxylase deficiency
    Eyal, Ori
    Tenenbaum-Rakover, Yardena
    Shalitin, Shlomit
    Israel, Shoshana
    Weintrob, Naomi
    ACTA PAEDIATRICA, 2013, 102 (04) : 419 - 423
  • [5] GENOTYPE AND HORMONAL PHENOTYPE IN NONCLASSICAL 21-HYDROXYLASE DEFICIENCY
    SPEISER, PW
    NEW, MI
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 64 (01): : 86 - 91
  • [6] Infertility and androgen excess in nonclassical 21-hydroxylase deficiency
    New, MI
    OVARY: REGULATION, DYSFUNCTION AND TREATMENT, 1996, 1106 : 195 - 198
  • [7] Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height
    Savas-Erdeve, Senay
    Cetinkaya, Semra
    Abali, Zehra Yavas
    Poyrazoglu, Sukran
    Bas, Firdevs
    Berberoglu, Merih
    Siklar, Zeynep
    Korkmaz, Ozlem
    Bulus, Derya
    Akbas, Emine Demet
    Guran, Tulay
    Bober, Ece
    Akin, Onur
    Yilmaz, Gulay Can
    Aycan, Zehra
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2017, 30 (07): : 759 - 766
  • [8] HIGH-FREQUENCY OF NONCLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY
    SPEISER, PW
    DUPONT, B
    RUBINSTEIN, P
    PIAZZA, A
    KASTELAN, A
    NEW, MI
    AMERICAN JOURNAL OF HUMAN GENETICS, 1985, 37 (04) : 650 - 667
  • [9] IDENTIFICATION OF NONCLASSICAL 21-HYDROXYLASE DEFICIENCY IN GIRLS WITH PRECOCIOUS PUBARCHE
    LEITE, MV
    MENDONCA, BB
    ARNHOLD, IJP
    ESTEFAN, V
    NUNES, C
    NICOLAU, W
    BLOISE, W
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1991, 14 (01): : 11 - 15
  • [10] A SEGREGATION AND LINKAGE STUDY OF CLASSICAL AND NONCLASSICAL 21-HYDROXYLASE DEFICIENCY
    SHERMAN, SL
    ASTON, CE
    MORTON, NE
    SPEISER, PW
    NEW, MI
    AMERICAN JOURNAL OF HUMAN GENETICS, 1988, 42 (06) : 830 - 838
12345