Literature DB >> 4357678

Familial congenital adrenal hypoplasia.

C G Brook, M Bambach, M Zachmann, A Prader.   

Abstract

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Year:  1973        PMID： 4357678

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


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  5 in total

1.  Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases.

Authors:  A Kohlschütter; H P Willig; D Schlamp; K Kruse; E R McCabe; H J Schäfer; G Beckenkamp; R Rohkamm
Journal:  Eur J Pediatr       Date:  1987-11       Impact factor: 3.183

2.  Gonadotrophin deficiency and adrenocortical insufficiency in children: a new syndrome.

Authors:  W F Kelly; G F Joplin; G W Pearson
Journal:  Br Med J       Date:  1977-07-09

3.  Isolated glucocorticoid deficiency.

Authors:  C Bianchi; B di Natale; G Trifirò; G Weber
Journal:  J Endocrinol Invest       Date:  1987-12       Impact factor: 4.256

4.  Progressive high frequency hearing loss: an additional feature in the syndrome of congenital adrenal hypoplasia and gonadotrophin deficiency.

Authors:  M Zachmann; E Fuchs; A Prader
Journal:  Eur J Pediatr       Date:  1992-03       Impact factor: 3.183

5.  Congenital adrenal hypoplasia: two new cases.

Authors:  R Virdis; L S Levine; D Levy; S Pang; R Rapaport; M I New
Journal:  J Endocrinol Invest       Date:  1983-02       Impact factor: 4.256
  5 in total

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