Literature DB >> 5101501

[Arterial hypertension, hypokalemic alkalosis and male pseudohermaphroditism caused by 17 alpha-hydroxylase deficiency].

F Mantero, B Busnardo, A Riondel, R Veyrat, M Austoni.   

Abstract

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Year:  1971        PMID： 5101501

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN： 0036-7672


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  5 in total

1.  17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.

Authors:  C Scaroni; A Biason; G Carpenè; G Opocher; F Mantero
Journal:  J Endocrinol Invest       Date:  1991-02       Impact factor: 4.256

Review 2.  Male hypogonadism.

Authors:  W D Odell; R S Swerdloff
Journal:  West J Med       Date:  1976-06

Review 3.  XY females with enzyme deficiencies of steroid metabolism. A brief review.

Authors:  K Madan; J Schoemaker
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Female phenotype in a male child due to 17-alpha-hydroxylase deficiency.

Authors:  G F Heremans; A J Moolenaar; H H van Gelderen
Journal:  Arch Dis Child       Date:  1976-09       Impact factor: 3.791

5.  Male pseudohermaphroditism: genetics and clinical delineation.

Authors:  J L Simpson
Journal:  Hum Genet       Date:  1978-10-19       Impact factor: 4.132
  5 in total

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