117 related articles for article (PubMed ID: 2375234)
1. An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population.
Dumić M; Brkljacić L; Speiser PW; Wood E; Crawford C; Plavsić V; Baniceviác M; Radmanović S; Radica A; Kastelan A
Acta Endocrinol (Copenh); 1990 Jun; 122(6):703-10. PubMed ID: 2375234
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
Speiser PW; New MI; White PC
N Engl J Med; 1988 Jul; 319(1):19-23. PubMed ID: 3260007
[TBL] [Abstract][Full Text] [Related]
3. Screening for non-classic 21-hydroxylase deficiency in an HLA-B14 positive population.
Motta P; Airaghi L; Catania A; Mangone I; Orsatti A; Tenconi L; Cantalamessa L; Zanussi C
Acta Endocrinol (Copenh); 1987 Oct; 116(2):211-5. PubMed ID: 2821719
[TBL] [Abstract][Full Text] [Related]
4. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype.
Libber SM; Migeon CJ; Bias WB
J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788
[TBL] [Abstract][Full Text] [Related]
5. HLA-B14 and nonclassical 21-hydroxylase deficiency in a heterogeneous New York population.
Levine LS
Ann N Y Acad Sci; 1985; 458():65-70. PubMed ID: 3879132
[No Abstract] [Full Text] [Related]
6. Isolated precocious pubarche: an approach.
Balducci R; Boscherini B; Mangiantini A; Morellini M; Toscano V
J Clin Endocrinol Metab; 1994 Aug; 79(2):582-9. PubMed ID: 8045980
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. '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; 109(3):386-92. PubMed ID: 2992207
[TBL] [Abstract][Full Text] [Related]
9. Detection of heterozygous carriers for 21-hydroxylase deficiency by plasma 21-deoxycortisol measurement.
Gourmelen M; Gueux B; Pham Huu Trung MT; Fiet J; Raux-Demay MC; Girard F
Acta Endocrinol (Copenh); 1987 Dec; 116(4):507-12. PubMed ID: 2827419
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.
Larizza D; Cuccia M; Martinetti M; Maghnie M; Dondi E; Salvaneschi L; Severi F
Clin Endocrinol (Oxf); 1994 Jan; 40(1):39-45. PubMed ID: 8306479
[TBL] [Abstract][Full Text] [Related]
12. The immunological detection of a 21-OH deficiency mutation HLA supratype.
Pollack MS; Keenan B; Christiansen FT; Cobain TJ; Dawkins RL; Clayton G
Am J Hum Genet; 1986 May; 38(5):688-98. PubMed ID: 3013005
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Late-onset type of 21-hydroxylase deficiency in childhood.
Roitman A; Stivel M; Zamir R; Kaufman H; Pertzelan A; Laron Z
Isr J Med Sci; 1982 Jul; 18(7):763-8. PubMed ID: 6980865
[TBL] [Abstract][Full Text] [Related]
15. 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; 53(6):1193-8. PubMed ID: 6271801
[TBL] [Abstract][Full Text] [Related]
16. High frequency of nonclassical steroid 21-hydroxylase deficiency.
Speiser PW; Dupont B; Rubinstein P; Piazza A; Kastelan A; New MI
Am J Hum Genet; 1985 Jul; 37(4):650-67. PubMed ID: 9556656
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.
New MI; Lorenzen F; Pang S; Gunczler P; Dupont B; Levine LS
J Clin Endocrinol Metab; 1979 Feb; 48(2):356-9. PubMed ID: 218988
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency.
Speiser PW; New MI; White PC
Endocr Res; 1989; 15(1-2):257-76. PubMed ID: 2788081
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]