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5. Clinical and endocrinological aspects of 21-hydroxylase deficiency. New MI Ann N Y Acad Sci; 1985; 458():1-27. PubMed ID: 3911845 [No Abstract] [Full Text] [Related]
6. Recent advances in 21-hydroxylase deficiency. New MI; Levine LS Annu Rev Med; 1984; 35():649-63. PubMed ID: 6372675 [TBL] [Abstract][Full Text] [Related]
7. [Genetic of the 21 hydroxylase deficiency]. Boué A; Couillin P; Pomarède R; Rappaport R; Boué J Ann Endocrinol (Paris); 1982; 43(1):3-14. PubMed ID: 6982657 [TBL] [Abstract][Full Text] [Related]
8. The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes. Cobain TJ; Stuckey MS; McCluskey J; Wilton AN; Gedeon A; Garlepp MJ; Christiansen FT; Dawkins RL Ann N Y Acad Sci; 1985; 458():76-84. PubMed ID: 3879134 [No Abstract] [Full Text] [Related]
9. HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France. Couillin P; Rappaport R; Kuttenn F; Hors J; Feingold J; Boué J; Boué A Ann N Y Acad Sci; 1985; 458():41-5. PubMed ID: 3879129 [No Abstract] [Full Text] [Related]
10. [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 [No Abstract] [Full Text] [Related]
11. HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population. Couillin P; Rappaport R; Kuttenn F; Canlorbe P; Hors J; Marcelli-Barge A; Feingold J; Grisard MC; Boué J; Boué A Tissue Antigens; 1982 Feb; 19(2):100-7. PubMed ID: 6980498 [No Abstract] [Full Text] [Related]
13. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations. Chrousos GP; Loriaux DL; Mann D; Cutler GB Horm Res; 1982; 16(4):193-200. PubMed ID: 6290362 [TBL] [Abstract][Full Text] [Related]
14. [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; 29(1):103-13. PubMed ID: 6977617 [No Abstract] [Full Text] [Related]
15. No linkage between HLA and congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. D'Armiento M; Reda G; Bisignani G; Tabolli S; Cappellaci S; Lulli P; Carbonara A; Biglieri EG N Engl J Med; 1983 Apr; 308(16):970-1. PubMed ID: 6601238 [No Abstract] [Full Text] [Related]
16. HLA associations in late-onset 21-hydroxylase deficiency in Israel. Laron Z; Roitman A; Pertzelan A; Kaufman H; Zamir R Ann N Y Acad Sci; 1985; 458():52-64. PubMed ID: 3879131 [No Abstract] [Full Text] [Related]
17. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients. Livieri C; Belvedere M; Martinetti M; Beluffi G; Fiori P; Cogliati CR; Goffredo V; Lorini R; Severi F Prog Clin Biol Res; 1985; 200():243-55. PubMed ID: 3001775 [No Abstract] [Full Text] [Related]
18. [Detection of heterozygotes in the classic type of congenital adrenal hyperplasia due to a 21-hydroxylase defect in our population as based on hormonal studies and HLA typing]. Dumić M; Tajić M; Brkljacić L; Mardesić D; Radica A; Lukenda M; Gjurić G; Jovanović V; Plavsić V; Kastelan A Lijec Vjesn; 1984; 106(11-12):466-70. PubMed ID: 6335215 [No Abstract] [Full Text] [Related]
19. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study. Kauschansky A; Kaufman H; Zamir R; Elian E Horm Res; 1981; 14(2):73-8. PubMed ID: 6268517 [No Abstract] [Full Text] [Related]
20. The biochemical basis for genotyping 21-hydroxylase deficiency. New MI; Dupont B; Pollack MS; Levine LS Hum Genet; 1981; 58(1):123-7. PubMed ID: 6269988 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]