169 related items for PubMed ID: 2982907
1. Genetic differences between the salt-wasting, simple virilizing, and nonclassical types of congenital adrenal hyperplasia.
Höller W, Scholz S, Knorr D, Bidlingmaier F, Keller E, Albert ED.
J Clin Endocrinol Metab; 1985 Apr; 60(4):757-63. PubMed ID: 2982907
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2. Different gene defects in the salt-wasting (SW), simple virilizing (SV), and nonclassical (NC) types of congenital adrenal hyperplasia (CAH).
Knorr D, Albert ED, Bidlingmaier F, Höller W, Scholz S.
Ann N Y Acad Sci; 1985 Apr; 458():71-5. PubMed ID: 3879133
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3. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.
J Clin Endocrinol Metab; 1985 Jul; 61(1):89-97. PubMed ID: 3873469
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4. Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studies.
Petersen KE, Svejgaard A, Nielsen MD, Dissing J.
Horm Res; 1982 Jul; 16(3):151-9. PubMed ID: 6286442
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5. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.
J Clin Endocrinol Metab; 1982 Nov; 55(5):866-71. PubMed ID: 6288754
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6. [HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population].
Couillin P, Ravisé N, Hors J, Feingold J, Rappaport R, Kuttenn F, Boué A.
Pathol Biol (Paris); 1986 Jun; 34(6):789-94. PubMed ID: 3531997
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7. Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening.
Sarafoglou K, Lorentz CP, Otten N, Oetting WS, Grebe SK.
Clin Genet; 2012 Jul; 82(1):64-70. PubMed ID: 21534945
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8. Late-onset adrenal hyperplasia in hirsutism.
Kuttenn F, Couillin P, Girard F, Billaud L, Vincens M, Boucekkine C, Thalabard JC, Maudelonde T, Spritzer P, Mowszowicz I.
N Engl J Med; 1985 Jul 25; 313(4):224-31. PubMed ID: 2989686
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9. 'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population.
Dumić M, Brkljacić L, Mardesić D, Plavsić V, Lukenda M, Kastelan A.
Acta Endocrinol (Copenh); 1985 Jul 25; 109(3):386-92. PubMed ID: 2992207
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10. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
J Clin Endocrinol Metab; 1981 Dec 25; 53(6):1193-8. PubMed ID: 6271801
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11. Genotype of classic congenital adrenal hyperplasia and the 60-minute adrenocorticotropic hormone stimulation test.
Tsai WY, Lee JS, Hsiao PH, Hsieh RP.
J Formos Med Assoc; 1995 Dec 25; 94(1-2):10-3. PubMed ID: 7613227
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12. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype.
Libber SM, Migeon CJ, Bias WB.
J Clin Endocrinol Metab; 1985 Apr 25; 60(4):727-30. PubMed ID: 3871788
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13. Pituitary-adrenal responses to corticotropin-releasing hormone in different degrees of adrenal 21-hydroxylase deficiency.
Moreira AC, Elias LL.
J Clin Endocrinol Metab; 1992 Jan 25; 74(1):198-203. PubMed ID: 1309366
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14. Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients.
Dain LB, Buzzalino ND, Oneto A, Belli S, Stivel M, Pasqualini T, Minutolo C, Charreau EH, Alba LG.
Clin Endocrinol (Oxf); 2002 Feb 25; 56(2):239-45. PubMed ID: 11874416
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15. Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.
Donohoue PA, Van Dop C, Migeon CJ, McLean RH, Bias WB.
J Clin Endocrinol Metab; 1987 Nov 25; 65(5):980-6. PubMed ID: 2822757
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16. Genetics and biochemical variability of variants of 21 hydroxylase deficiency.
Gordon MT, Conway DI, Anderson DC, Harris R.
J Med Genet; 1985 Oct 25; 22(5):354-60. PubMed ID: 3001309
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17. [Analysis of the association of HLA-DQ1 alleles with mutation of the 21-hydroxylase gene in patients with congenital adrenal hyperplasia].
Osinovskaia NS, Ivashchenko TE, Baranov VS.
Genetika; 2004 Jan 25; 40(1):97-101. PubMed ID: 15027205
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18. HLA associations in patients with polycystic ovaries and in patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency.
Hague WM, Adams J, Algar V, Drummond V, Schwarz G, Bottazzo GF, Jacobs HS.
Clin Endocrinol (Oxf); 1990 Apr 25; 32(4):407-15. PubMed ID: 2347091
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19. Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia.
Fiet J, Gueux B, Gourmelen M, Kuttenn F, Vexiau P, Couillin P, Pham-Huu-Trung MT, Villette JM, Raux-Demay MC, Galons H.
J Clin Endocrinol Metab; 1988 Apr 25; 66(4):659-67. PubMed ID: 2831244
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20. HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiency.
Einaudi S, Borelli I, Lala R, Praticŏ L, Curtoni ES, De Sanctis C.
J Pediatr Endocrinol; 1994 Apr 25; 7(4):349-55. PubMed ID: 7735374
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