Literature DB >> 3097413

Neonatal screening programme for congenital adrenal hyperplasia in a homogeneous Caucasian population.

E Cacciari, A Balsamo, A Cassio, S Piazzi, F Bernardi, S Salardi, A Cicognani, P Pirazzoli, F Zappulla, M Capelli.   

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Year:  1986        PMID: 3097413     DOI: 10.1007/bf01800868

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


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  12 in total

1.  [Incidence of congenital adrenogenital syndrome].

Authors:  A PRADER
Journal:  Helv Paediatr Acta       Date:  1958-11

2.  Virilizing adrenal hyperplasia; a genetic and hormonal study.

Authors:  B CHILDS; M M GRUMBACH; J J VAN WYK
Journal:  J Clin Invest       Date:  1956-02       Impact factor: 14.808

3.  Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia.

Authors:  S Pang; J Hotchkiss; A L Drash; L S Levine; M I New
Journal:  J Clin Endocrinol Metab       Date:  1977-11       Impact factor: 5.958

4.  Incidence of salt-losing form of congenital virilizing adrenal hyperplasia.

Authors:  Q H Qazi; M W Thompson
Journal:  Arch Dis Child       Date:  1972-04       Impact factor: 3.791

5.  An unusually high incidence of salt-losing congenital adrenal hyperplasia in the Alaskan Eskimo.

Authors:  A J Hirschfeld; J K Fleshman
Journal:  J Pediatr       Date:  1969-09       Impact factor: 4.406

6.  Neonatal screening for congenital adrenal hyperplasia.

Authors:  E Cacciari; A Balsamo; A Cassio; S Piazzi; F Bernardi; S Salardi; A Cicognani; P Pirazzoli; F Zappulla; M Capelli
Journal:  Arch Dis Child       Date:  1983-10       Impact factor: 3.791

7.  Neonatal screening for congenital adrenal hyperplasia using a microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay. Experience gained from the study of 22,233 cases.

Authors:  E Cacciari; A Balsamo; A Cassio; S Piazzi; F Bernardi; S Salardi; A Cicognani; P Pirazzoli; F Zappulla; M Capelli; M Paolini
Journal:  Horm Res       Date:  1982

8.  Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group.

Authors:  L S Levine; M Zachmann; M I New; A Prader; M S Pollack; G J O'Neill; S Y Yang; S E Oberfield; B Dupont
Journal:  N Engl J Med       Date:  1978-10-26       Impact factor: 91.245

9.  Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  M Zachmann; A Prader
Journal:  Acta Endocrinol (Copenh)       Date:  1978-03

10.  Adult-onset familial adrenal 21-hydroxylase deficiency.

Authors:  J Blankstein; C Faiman; F I Reyes; M L Schroeder; J S Winter
Journal:  Am J Med       Date:  1980-03       Impact factor: 4.965

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  1 in total

1.  Value of selective screening for congenital adrenal hyperplasia in Hungary.

Authors:  J Sólyom; I A Hughes
Journal:  Arch Dis Child       Date:  1989-03       Impact factor: 3.791

  1 in total

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