124 related articles for article (PubMed ID: 494231)
1. HLA and congenital adrenal hyperplasia due to 11-hydroxylase deficiency.
Glenthøj A; Nielsen MD; Starup J; Svejgaard A
Tissue Antigens; 1979 Aug; 14(2):181-2. PubMed ID: 494231
[No Abstract] [Full Text] [Related]
2. Detection of heterozygote of 21-hydroxylase deficiency.
Sobel DO; Gutai JP; Jones JC; Wagener DK; Smith W
Lancet; 1980 Jan; 1(8158):47. PubMed ID: 6101388
[No Abstract] [Full Text] [Related]
3. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
Dumić M; Brkljacić L; Krzisnik C; Radica A; Tajić M; Kastelan A
Lijec Vjesn; 1983; 105(7-8):290-2. PubMed ID: 6605467
[No Abstract] [Full Text] [Related]
4. Genetic linkage and HLA association in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Sobel DO; Gutai JP; Wagener DK; Jones JC; Smith WI; Strong DM
Hum Immunol; 1983 May; 7(1):35-44. PubMed ID: 6602118
[TBL] [Abstract][Full Text] [Related]
5. [HL-A associated inheritance of the 21-hydroxylase defect in familial adrenogenital syndrome].
Johannsen R; Laube H; Graef V; Pernice W
Verh Dtsch Ges Inn Med; 1978; (84):1412-6. PubMed ID: 741981
[No Abstract] [Full Text] [Related]
6. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).
Dupont B; Oberfield SE; Smithwick EM; Lee TD; Levine LS
Lancet; 1977 Dec 24-31; 2(8052-8053):1309-12. PubMed ID: 74726
[TBL] [Abstract][Full Text] [Related]
7. [Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)].
Bartolotta E; Migliori C; Gabrielli A; Oggiano N; Catassi C; Leone L
Pediatr Med Chir; 1981; 3(4):287-90. PubMed ID: 6283486
[No Abstract] [Full Text] [Related]
8. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typing.
Zachmann M; Prader A
Acta Endocrinol (Copenh); 1979 Nov; 92(3):542-6. PubMed ID: 517053
[TBL] [Abstract][Full Text] [Related]
9. No linkage between HLA and congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency.
Mantero F; Scaroni C; Pasini CV; Fagiolo U
N Engl J Med; 1980 Aug; 303(9):530. PubMed ID: 6967187
[No Abstract] [Full Text] [Related]
10. 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]
11. [21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive].
Simonin G; Palix C; Roulier R; Coignet J
Ann Pediatr (Paris); 1986 May; 33(5):423-7. PubMed ID: 3729253
[No Abstract] [Full Text] [Related]
12. [HLA haplotypes in congenital adrenal hyperplasia (21-hydroxylase deficiency].
González-Díaz JP; González T; González-Espinosa C; Gantes M; Santisteban M; Bustad S
An Esp Pediatr; 1984 Oct; 21(6):583-6. PubMed ID: 6335362
[TBL] [Abstract][Full Text] [Related]
13. [Detection of heterozygous carriers of 21-hydroxylase deficiency-HLA typing and endocrinological study (author's transl)].
Saito N; Kuribayashi T; Shimozawa K; Nakagawa S; Tomita M
Horumon To Rinsho; 1980 Jul; 28(7):767-72. PubMed ID: 7460327
[No Abstract] [Full Text] [Related]
14. Prenatal diagnosis of congenital adrenal hyperplasia.
Marcus ES; Holcombe JH; Tulchinsky D; Rich RR; Riccardi VM
Am J Med Genet; 1979; 4(2):201-4. PubMed ID: 517576
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients.
Fleischnick E; Awdeh ZL; Raum D; Granados J; Alosco SM; Crigler JF; Gerald PS; Giles CM; Yunis EJ; Alper CA
Lancet; 1983 Jan; 1(8317):152-6. PubMed ID: 6130199
[TBL] [Abstract][Full Text] [Related]
17. The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: possible linkage between HLA and the neuraminidase deficiency gene.
Oohira T; Nagata N; Akaboshi I; Matsuda I; Naito S
Hum Genet; 1985; 70(4):341-3. PubMed ID: 3874816
[TBL] [Abstract][Full Text] [Related]
18. 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]
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. 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]
[Next] [New Search]
