Literature DB >> 1806617

On the antenatal diagnosis of 17-hydroxylase deficiency.

E Reschini, A Catania, A D'Alberton.   

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Year:  1991        PMID: 1806617     DOI: 10.1007/BF03347130

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


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  6 in total

Review 1.  17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition.

Authors:  T Yanase; E R Simpson; M R Waterman
Journal:  Endocr Rev       Date:  1991-02       Impact factor: 19.871

2.  Male pseudohermaphroditism due to 17-hydroxylase deficiency.

Authors:  A D'Alberton; E Reschini; T Motta; A Catania
Journal:  J Endocrinol Invest       Date:  1989-03       Impact factor: 4.256

3.  Congenital idiopathic adrenal hypoplasia.

Authors:  C R Laverty; D W Fortune; N A Beischer
Journal:  Obstet Gynecol       Date:  1973-05       Impact factor: 7.661

4.  Spontaneous remission of Cushing syndrome after termination of pregnancy.

Authors:  E Reschini; G Giustina; P G Crosignani; A D'Alberton
Journal:  Obstet Gynecol       Date:  1978-05       Impact factor: 7.661

5.  Diagnosis and natural history of 17-hydroxylase deficiency in a newborn male.

Authors:  H J Dean; C H Shackleton; J S Winter
Journal:  J Clin Endocrinol Metab       Date:  1984-09       Impact factor: 5.958

6.  A new cause of female pseudohermaphroditism: placental aromatase deficiency.

Authors:  M Shozu; K Akasofu; T Harada; Y Kubota
Journal:  J Clin Endocrinol Metab       Date:  1991-03       Impact factor: 5.958

  6 in total

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