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Journal Abstract Search

163 related items for PubMed ID: 3493478

  • 1. [Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Boutte P, Madar H, d'Ollone M, Ferracci JP, Bebin B, Lambert JC, Sebag F.
    Pediatrie; 1986; 41(7):559-64. PubMed ID: 3493478
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  • 2. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers].
    Dumić M, Plavsić V, Brkljacić L, Sarnavka V, Mardesić D, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Apr; 105(4):145-9. PubMed ID: 6602259
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  • 3. [Genetic counseling in the adrenogenital syndrome caused by 2I-hydroxylase deficiency].
    Breuning MH, Maaswinkel-Mooy PD.
    Ned Tijdschr Geneeskd; 1986 Aug 30; 130(35):1552-5. PubMed ID: 3489897
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  • 5. [Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].
    Bouchard M, Forest MG, David M, Dechaud H, Juif JG.
    Pediatrie; 1989 Aug 30; 44(8):637-40. PubMed ID: 2622705
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  • 7. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar 30; 29(1):103-13. PubMed ID: 6977617
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  • 8. [Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. A clinical case].
    Zacharías S, Contreras P.
    Rev Chil Obstet Ginecol; 1984 Mar 30; 49(5):295-9. PubMed ID: 6242254
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  • 11. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 30; 65(4):777-81. PubMed ID: 6966049
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  • 18. [Congenital virilization in a newborn girl of a mother with adrenogenital syndrome due to 21-hydroxylase deficiency].
    Ferrante L.
    Minerva Pediatr; 1976 Jun 23; 28(22):1443-4. PubMed ID: 986003
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  • 20. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG, Brykova EK, Bakharev VA.
    Akush Ginekol (Mosk); 1990 Jan 23; (1):10-4. PubMed ID: 2353725
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