108 related articles for article (PubMed ID: 6283486)
1. [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]
2. [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]
3. 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]
4. Late onset congenital adrenal hyperplasia in a Puerto Rican family: hormonal and HLA typing.
Hernán Martínez J; Riestra JL
Bol Asoc Med P R; 1986 Nov; 78(11):472-6. PubMed ID: 3026413
[No Abstract] [Full Text] [Related]
5. 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]
6. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
Pang S; Levine LS; Lorenzen F; Chow D; Pollack M; Dupont B; Genel M; New MI
J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
Stuckey MS; Boyne P; Macdonald WB; Christiansen FT; Houliston JB; Dawkins RL
Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
[TBL] [Abstract][Full Text] [Related]
10. Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Lorenzen F; Pang S; New M; Pollack M; Oberfield S; Dupont B; Chow D; Schneider B; Levine L
J Clin Endocrinol Metab; 1980 Mar; 50(3):572-7. PubMed ID: 6244326
[No Abstract] [Full Text] [Related]
11. 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]
12. [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]
13. [A genetic and hormonal study of 5 patients with the nonclassical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
Velasco FJ; Picó AM; Muñoz C; Mauri M; de la Sen ML
Med Clin (Barc); 1992 Jun; 99(3):81-6. PubMed ID: 1321317
[TBL] [Abstract][Full Text] [Related]
14. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.
Laron Z; Pollack MS; Zamir R; Roitman A; Dickerman Z; Levine LS; Lorenzen F; O'Neill GJ; Pang S; New MI; Dupont B
Hum Immunol; 1980 Jul; 1(1):55-66. PubMed ID: 6266983
[No Abstract] [Full Text] [Related]
15. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
Colle M; Battin J
Arch Fr Pediatr; 1984; 41(7):483-5. PubMed ID: 6333857
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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; 16(3):151-9. PubMed ID: 6286442
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. [Genetic aspects in congenital adrenal hyperplasia (author's transl)].
Zachmann M; Prader A
Schweiz Rundsch Med Prax; 1977 Jul; 66(27):809-13. PubMed ID: 896655
[No Abstract] [Full Text] [Related]
[Next] [New Search]