Literature DB >> 9221273

11 Beta-hydroxylase deficiency.

F Mantero1, G Opocher, D Armanini, S Filipponi.   

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Year:  1995        PMID: 9221273     DOI: 10.1007/bf03349766

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


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  18 in total

1.  Congenital adrenal hyperplasia with hypertension: unusual steroid pattern in blood and urine.

Authors:  W R EBERLEIN; A M BONGIOVANNI
Journal:  J Clin Endocrinol Metab       Date:  1955-12       Impact factor: 5.958

2.  A hybrid cell mapping panel for regional localization of probes to human chromosome 8.

Authors:  M J Wagner; Y Ge; M Siciliano; D E Wells
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

3.  High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from Morocco.

Authors:  A Rösler; E Leiberman; T Cohen
Journal:  Am J Med Genet       Date:  1992-04-01

4.  Case of adrenogenital syndrome with hypertension treated with cortisone.

Authors:  T H SHEPARD; S W CLAUSEN
Journal:  Pediatrics       Date:  1951-12       Impact factor: 7.124

5.  11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.

Authors:  A Rösler; N Weshler; E Leiberman; Z Hochberg; J Weidenfeld; J Sack; J Chemke
Journal:  J Clin Endocrinol Metab       Date:  1988-04       Impact factor: 5.958

6.  Steroid 11 beta-hydroxylase deficiency caused by a five base pair duplication in the CYP11B1 gene.

Authors:  C A Skinner; G Rumsby
Journal:  Hum Mol Genet       Date:  1994-02       Impact factor: 6.150

7.  Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta).

Authors:  E Mornet; J Dupont; A Vitek; P C White
Journal:  J Biol Chem       Date:  1989-12-15       Impact factor: 5.157

8.  A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.

Authors:  P C White; J Dupont; M I New; E Leiberman; Z Hochberg; A Rösler
Journal:  J Clin Invest       Date:  1991-05       Impact factor: 14.808

9.  Frame shift by insertion of 2 basepairs in codon 394 of CYP11B1 causes congenital adrenal hyperplasia due to steroid 11 beta-hydroxylase deficiency.

Authors:  A Helmberg; B Ausserer; R Kofler
Journal:  J Clin Endocrinol Metab       Date:  1992-11       Impact factor: 5.958

10.  Therapeutic effect of calcium channel blockade in primary aldosteronism.

Authors:  J L Nadler; W Hsueh; R Horton
Journal:  J Clin Endocrinol Metab       Date:  1985-05       Impact factor: 5.958

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  2 in total

Review 1.  Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Authors:  Krupali Bulsari; Henrik Falhammar
Journal:  Endocrine       Date:  2016-12-07       Impact factor: 3.633

2.  Diagnosis of immune thrombocytopenia, including secondary forms, and selection of second-line treatment.

Authors:  James B Bussel; Christine A Garcia
Journal:  Haematologica       Date:  2022-09-01       Impact factor: 11.047

  2 in total

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