Literature DB >> 4258797

Further in vivo studies in male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect (compared to a case of testicular feminization).

J M Saez, A M Morera, E De Peretti, J Bertrand.   

Abstract

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Year:  1972        PMID： 4258797     DOI： 10.1210/jcem-34-3-598

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


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  11 in total

1.  Ultrastructural study of testis in testicular feminization.

Authors:  K Kovacs; A Chalvardjian; E Horvath; W Steinberg
Journal:  Arch Gynakol       Date:  1976-12-10

Review 2.  Male hypogonadism.

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

Review 3.  Endocrine findings in male pseudohermaphroditism.

Authors:  M Zachmann
Journal:  Eur J Pediatr       Date:  1993       Impact factor: 3.183

Review 4.  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

Review 5.  Clinical, endocrine, and molecular findings in 17beta-hydroxysteroid dehydrogenase type 3 deficiency.

Authors:  M F Faienza; L Giordani; M Delvecchio; L Cavallo
Journal:  J Endocrinol Invest       Date:  2008-01       Impact factor: 4.256

6.  Prepubertal male pseudohermaphroditism due to 17-ketosteroid reductase deficiency: diagnostic value of a hCG test and lack of HLA association.

Authors:  I J Arnhold; B B Mendonça; J A Diaz; C Nogueira; M C Batista; G Madureira; D Oliveira; W Nicolau; W Bloise
Journal:  J Endocrinol Invest       Date:  1988-04       Impact factor: 4.256

7.  Male pseudohermaphroditism: genetics and clinical delineation.

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

8.  17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite.

Authors:  Lindsay M Mains; Babak Vakili; Yves Lacassie; Stefan Andersson; Annika Lindqvist; John A Rock
Journal:  Fertil Steril       Date:  2007-05-16       Impact factor: 7.329

9.  46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin.

Authors:  Assimina Galli-Tsinopoulou; Anastasios Serbis; Eleni P Kotanidou; Eleni Litou; Vaia Dokousli; Konstantina Mouzaki; Pavlos Fanis; Vassos Neocleous; Nicos Skordis
Journal:  J Clin Res Pediatr Endocrinol       Date:  2017-07-24

10.  Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene.

Authors:  Ayfer Alikaşifoğlu; Doğuş Vurallı; Olaf Hiort; Nazlı Gönç; Alev Özön; Nurgün Kandemir
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-09
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