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Journal Abstract Search

137 related items for PubMed ID: 2139596

  • 1. Late onset adrenal hyperplasia in a group of Irish females who presented with hirsutism, irregular menses and/or cystic acne.
    McLaughlin B, Barrett P, Finch T, Devlin JG.
    Clin Endocrinol (Oxf); 1990 Jan; 32(1):57-64. PubMed ID: 2139596
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  • 2. 21-Hydroxylase deficiency in female hyperandrogenism: screening and diagnosis.
    Azziz R, Zacur HA.
    J Clin Endocrinol Metab; 1989 Sep; 69(3):577-84. PubMed ID: 2547827
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  • 3. The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women.
    Chetkowski RJ, DeFazio J, Shamonki I, Judd HL, Chang RJ.
    J Clin Endocrinol Metab; 1984 Apr; 58(4):595-8. PubMed ID: 6321532
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  • 4. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.
    Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF.
    Pediatrics; 1983 Nov; 72(5):690-5. PubMed ID: 6314235
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  • 6. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
    Chrousos GP, Loriaux DL, Mann D, Cutler GB.
    Horm Res; 1982 Nov; 16(4):193-200. PubMed ID: 6290362
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  • 8. Screening for late-onset congenital adrenal hyperplasia in hirsutism or amenorrhea.
    Baskin HJ.
    Arch Intern Med; 1987 May; 147(5):847-8. PubMed ID: 3579438
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  • 9. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
    Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904
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  • 12. Adrenal androgen hyperresponsiveness to adrenocorticotropin in women with acne and/or hirsutism: adrenal enzyme defects and exaggerated adrenarche.
    Lucky AW, Rosenfield RL, McGuire J, Rudy S, Helke J.
    J Clin Endocrinol Metab; 1986 May; 62(5):840-8. PubMed ID: 3007557
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  • 14. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.
    Chrousos GP, Loriaux DL, Mann DL, Cutler GB.
    Ann Intern Med; 1982 Feb; 96(2):143-8. PubMed ID: 6977282
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  • 16. Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. A study of five cases.
    Bouchard P, Kuttenn F, Mowszowicz I, Schaison G, Raux-Eurin MC, Mauvais-Jarvis P.
    Acta Endocrinol (Copenh); 1981 Jan; 96(1):107-11. PubMed ID: 6257014
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  • 20. Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women.
    Carmina E, Dewailly D, Escobar-Morreale HF, Kelestimur F, Moran C, Oberfield S, Witchel SF, Azziz R.
    Hum Reprod Update; 2017 Sep 01; 23(5):580-599. PubMed ID: 28582566
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