Literature DB >> 6244328

Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.

S Pang, L S Levine, F Lorenzen, D Chow, M Pollack, B Dupont, M Genel, M I New.   

Abstract

Hormonal response to ACTH stimulation and HLA genotyping were determined in families of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia. Neither hormonal measurements nor HLA genotyping were useful for the detection of heterozygosity in the families.

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Year:  1980        PMID： 6244328     DOI： 10.1210/jcem-50-3-586

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


  4 in total

Review 1.  11 Beta-hydroxylase deficiency.

Authors:  F Mantero; G Opocher; D Armanini; S Filipponi
Journal:  J Endocrinol Invest       Date:  1995 Jul-Aug       Impact factor: 4.256

2.  Low-renin primary hypertension in a young patient treated with dexamethasone.

Authors:  A P Tommaselli; G De Simone; L Di Lorenzo; R Rossi; A Cocca; R Valentino; B Biondi; G Lombardi
Journal:  J Endocrinol Invest       Date:  1986-02       Impact factor: 4.256

Review 3.  Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Authors:  Krupali Bulsari; Henrik Falhammar
Journal:  Endocrine       Date:  2016-12-07       Impact factor: 3.633

4.  Use of Successive Pharmacologic Hormone Suppression Testing for a Severe Presentation of Adolescent Polycystic Ovarian Syndrome: A Case Report.

Authors:  Sonalee Jaya Ravi; Melanie Cree-Green
Journal:  J Investig Med High Impact Case Rep       Date:  2019 Jan-Dec
  4 in total

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