GENOTYPE AND HORMONAL PHENOTYPE IN NONCLASSICAL 21-HYDROXYLASE DEFICIENCY

被引:62
作者
SPEISER, PW
NEW, MI
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D O I
10.1210/jcem-64-1-86
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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页码:86 / 91
页数:6
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  • [1] ADULT-ONSET FAMILIAL ADRENAL 21-HYDROXYLASE DEFICIENCY
    BLANKSTEIN, J
    FAIMAN, C
    REYES, FI
    SCHROEDER, ML
    WINTER, JSD
    [J]. AMERICAN JOURNAL OF MEDICINE, 1980, 68 (03) : 441 - 448
  • [2] CONGENITAL ADRENAL-HYPERPLASIA DUE TO PARTIAL 21-HYDROXYLASE DEFICIENCY - A STUDY OF 5 CASES
    BOUCHARD, P
    KUTTENN, F
    MOWSZOWICZ, I
    SCHAISON, G
    RAUXEURIN, MC
    MAUVAISJARVIS, P
    [J]. ACTA ENDOCRINOLOGICA, 1981, 96 (01): : 107 - 111
  • [3] Danilovs J., 1980, HISTOCOMPATIBILITY T, P287
  • [4] DECOURT J, 1957, Ann Endocrinol (Paris), V18, P416
  • [5] DUPONT B, 1977, LANCET, V2, P1309
  • [6] DETECTION OF HETEROZYGOUS CARRIER FOR CONGENITAL VIRILIZING ADRENAL-HYPERPLASIA
    GUTAI, JP
    KOWARSKI, AA
    MIGEON, CJ
    [J]. JOURNAL OF PEDIATRICS, 1977, 90 (06) : 924 - 929
  • [7] JONES GES, 1953, FERTIL STERIL, V4, P49
  • [8] KLOUDA PT, 1978, LANCET, V2, P1046
  • [9] LATE-ONSET STEROID 21-HYDROXYLASE DEFICIENCY - A VARIANT OF CLASSICAL CONGENITAL ADRENAL-HYPERPLASIA
    KOHN, B
    LEVINE, LS
    POLLACK, MS
    PANG, S
    LORENZEN, F
    LEVY, D
    LERNER, AJ
    RONDANINI, GF
    DUPONT, B
    NEW, MI
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1982, 55 (05) : 817 - 827
  • [10] SERUM ANDROGENS AS A CONTINUING INDEX OF ADEQUACY OF TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA
    KORTHSCHUTZ, S
    VIRDIS, R
    SAENGER, P
    CHOW, DM
    LEVINE, LS
    NEW, MI
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1978, 46 (03) : 452 - 458