Literature DB >> 6266983

Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.

Z Laron, M S Pollack, R Zamir, A Roitman, Z Dickerman, L S Levine, F Lorenzen, G J O'Neill, S Pang, M I New, B Dupont.   

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Year:  1980        PMID： 6266983     DOI： 10.1016/0198-8859(80)90009-9

Source DB:  PubMed          Journal:  Hum Immunol        ISSN： 0198-8859            Impact factor:   2.850


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  12 in total

Review 1.  Hirsutism: pilosebaceous unit dysregulation. Role of peripheral and glandular factors.

Authors:  V Toscano
Journal:  J Endocrinol Invest       Date:  1991-02       Impact factor: 4.256

2.  High frequency of nonclassical steroid 21-hydroxylase deficiency.

Authors:  P W Speiser; B Dupont; P Rubinstein; A Piazza; A Kastelan; M I New
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

Review 3.  The Gordon Wilson Lecture. Congenital adrenal hyperplasia.

Authors:  M I New
Journal:  Trans Am Clin Climatol Assoc       Date:  1991

4.  Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.

Authors:  M I New; R C Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

5.  HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.

Authors:  M S Pollack; M I New; G J O'Neill; L S Levine; C Callaway; S Pang; E Cacciari; F Mantero; A Cassio; C Scaroni; G Chiumello; G F Rondanini; L Gargantini; G Giovannelli; R Virdis; E Bartolotta; C Migliori; C Pintor; L Tato; F Barboni; B Dupont
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  New reliable biochemical marker for screening 21 alpha-hydroxylase deficiency without index person among hirsute women in agreement with HLA-haplotyping.

Authors:  A Chryssikopoulos; I Phocas; A Sarandakou; E Trakakis; D Rizos
Journal:  J Endocrinol Invest       Date:  1995-11       Impact factor: 4.256

7.  HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).

Authors:  C Scaroni; E Orlandini; C Venturi Pasini; M Gangemi; F Mantero
Journal:  J Endocrinol Invest       Date:  1986-02       Impact factor: 4.256

8.  Genetics and biochemical variability of variants of 21 hydroxylase deficiency.

Authors:  M T Gordon; D I Conway; D C Anderson; R Harris
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

9.  The immunological detection of a 21-OH deficiency mutation HLA supratype.

Authors:  M S Pollack; B Keenan; F T Christiansen; T J Cobain; R L Dawkins; G Clayton
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

10.  HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

Authors:  M S Pollack; L S Levine; G J O'Neill; S Pang; F Lorenzen; B Kohn; G F Rondanini; G Chiumello; M I New; B Dupont
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025
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