Literature DB >> 8989231

17 alpha-Hydroxylase deficiency: 1963-1966.

E G Biglieri1.   

Abstract

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Year:  1997        PMID: 8989231     DOI: 10.1210/jcem.82.1.3653

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


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  6 in total

Review 1.  Genetics of the adrenal gland.

Authors:  Constantine A Stratakis; Ioannis Bossis
Journal:  Rev Endocr Metab Disord       Date:  2004-03       Impact factor: 6.514

Review 2.  Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic.

Authors:  Richard J Auchus
Journal:  J Steroid Biochem Mol Biol       Date:  2016-02-06       Impact factor: 4.292

Review 3.  Genetics of hypertension: an assessment of progress in the spontaneously hypertensive rat.

Authors:  Peter A Doris
Journal:  Physiol Genomics       Date:  2017-09-15       Impact factor: 3.107

Review 4.  Physiological basis for the etiology, diagnosis, and treatment of adrenal disorders: Cushing's syndrome, adrenal insufficiency, and congenital adrenal hyperplasia.

Authors:  Hershel Raff; Susmeeta T Sharma; Lynnette K Nieman
Journal:  Compr Physiol       Date:  2014-04       Impact factor: 9.090

5.  Antenatal betamethasone depresses maternal and fetal aldosterone levels.

Authors:  Julie M Kessel; Jackie M Cale; Erin Verbrick; C Richard Parker; David P Carlton; Ian M Bird
Journal:  Reprod Sci       Date:  2009-01       Impact factor: 3.060

6.  17-α-Hydroxylase deficiency: An unusual case with primary amenorrhea and hypertension.

Authors:  Sunil Kumar Kota; Kirtikumar Modi; Ratan Jha; Surya Narayan Mandal
Journal:  Indian J Endocrinol Metab       Date:  2011-04
  6 in total

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