245 related articles for article (PubMed ID: 3320531)
1. Basic and clinical aspects of congenital adrenal hyperplasia.
New MI
J Steroid Biochem; 1987; 27(1-3):1-7. PubMed ID: 3320531
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetics and the characterization of steroid 21-hydroxylase deficiency.
New MI
Endocr Res; 1986; 12(4):505-22. PubMed ID: 3030723
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genetics of adrenal steroid 21-hydroxylase deficiency.
New MI; Speiser PW
Endocr Rev; 1986 Aug; 7(3):331-49. PubMed ID: 3527688
[TBL] [Abstract][Full Text] [Related]
6. [New concepts in virilizing adrenal hyperplasia caused by 21-hydroxylase block].
Cortínez A; Beas F; Devoto L; Henríquez C
Rev Chil Pediatr; 1985; 56(3):192-8. PubMed ID: 3879364
[No Abstract] [Full Text] [Related]
7. 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]
8. [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]
9. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].
Lambotte C
Rev Med Liege; 1986 Jan; 41(2):37-44. PubMed ID: 3006204
[No Abstract] [Full Text] [Related]
10. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
Couillin P
Presse Med; 1984 Apr; 13(17):1087-90. PubMed ID: 6232534
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
Mornet E; Boue J; Raux-Demay M; Couillin P; Oury JF; Dumez Y; Dausset J; Cohen D; Boué A
Hum Genet; 1986 Aug; 73(4):358-64. PubMed ID: 3017844
[TBL] [Abstract][Full Text] [Related]
13. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
Kohn B; Levine LS; Pollack MS; Pang S; Lorenzen F; Levy D; Lerner AJ; Rondanini GF; Dupont B; New MI
J Clin Endocrinol Metab; 1982 Nov; 55(5):817-27. PubMed ID: 6288753
[TBL] [Abstract][Full Text] [Related]
14. The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.
Kastelan A; Brkljacić-Surkalović L; Dumić M
Ann N Y Acad Sci; 1985; 458():36-40. PubMed ID: 3879128
[No Abstract] [Full Text] [Related]
15. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
Levine LS; Dupont B; Lorenzen F; Pang S; Pollack M; Oberfield S; 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; 1980 Dec; 51(6):1316-24. PubMed ID: 6449518
[TBL] [Abstract][Full Text] [Related]
16. [Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency].
Dumić M; Ille J; Brkljacić L; Plavsić V; Drazancić A; Banicević M; Radmanović S; Filipović B; Suchanek E; Kastelan A
Lijec Vjesn; 1989; 111(9-10):312-7. PubMed ID: 2633007
[TBL] [Abstract][Full Text] [Related]
17. Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment.
Carlson AD; Obeid JS; Kanellopoulou N; Wilson RC; New MI
J Steroid Biochem Mol Biol; 1999; 69(1-6):19-29. PubMed ID: 10418977
[TBL] [Abstract][Full Text] [Related]
18. Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.
O'Neill GJ; Dupont B; Pollack MS; Levine LS; New MI
Clin Immunol Immunopathol; 1982 May; 23(2):312-22. PubMed ID: 6980755
[No Abstract] [Full Text] [Related]
19. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Layrisse Z; White C; Gunczler P; Gafaro Valera L; Arias S; Yunis EJ; Alper CA; Awdeh ZL
Immunogenetics; 1987; 25(2):99-103. PubMed ID: 3493216
[TBL] [Abstract][Full Text] [Related]
20. [Genetic aspects of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
Leheup BP; Pierson M
J Genet Hum; 1987 May; 35(2-3):145-58. PubMed ID: 3497223
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
