Literature DB >> 5059525

Difficulties in the diagnosis of the adrenogenital syndrome in infancy.

C H Shackleton, F L Mitchell, J W Farquhar.   

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Year:  1972        PMID： 5059525

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  6 in total

1.  Early diagnosis of salt-losing congenital adrenal hyperplasia in a newborn boy.

Authors:  I A Hughes; J S Winter
Journal:  Can Med Assoc J       Date:  1977-08-20       Impact factor: 8.262

Review 2.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.

Authors:  G E Bacon; R P Kelch
Journal:  J Endocrinol Invest       Date:  1979 Jan-Mar       Impact factor: 4.256

3.  Plasma 17-hydroxyprogesterone in newborn infants with congenital adrenal hyperplasia and in infants with normal adrenal function.

Authors:  S M Atherden; A T Edmunds; D B Grant
Journal:  Arch Dis Child       Date:  1974-03       Impact factor: 3.791

4.  Familial glucocorticoid deficiency. Studies of diagnosis and pathogenesis.

Authors:  D Thistlethwaite; J A Darling; R Fraser; P A Mason; L H Rees; R A Harkness
Journal:  Arch Dis Child       Date:  1975-04       Impact factor: 3.791

5.  Neonatal screening for 21-hydroxylase deficiency: a microfilter paper method for 17-alpha-hydroxyprogesterone assay.

Authors:  S Piazzi; M Capelli; M Paolini; D Perugini; G Grossi; A Balsamo; P Salomoni; A Cassio; G Bugiardini; E Cacciari
Journal:  J Endocrinol Invest       Date:  1982 Mar-Apr       Impact factor: 4.256

6.  Increased urinary excretion of total 16 alpha-hydroxypregnenolone in newborn infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  J Homoki; W M Teller
Journal:  Klin Wochenschr       Date:  1982-04-15
  6 in total

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