BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 517053)

  • 1. 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]  

  • 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. [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]  

  • 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; 16(3):151-9. PubMed ID: 6286442
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Zachmann M; Prader A
    Acta Endocrinol (Copenh); 1978 Mar; 87(3):557-65. PubMed ID: 580145
    [TBL] [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. 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]  

  • 8. [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]  

  • 9. 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]  

  • 10. 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]  

  • 11. [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]  

  • 12. 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]  

  • 13. [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]  

  • 14. [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]  

  • 15. 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]  

  • 16. '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]  

  • 17. [Detection of heterozygosity in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the general population].
    Dumić M; Lukenda M; Plavsić V; Brkljacić L; Jovanović V; Kastelan A
    Lijec Vjesn; 1990; 112(5-6):138-41. PubMed ID: 2172673
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.
    Pollack MS; Maurer D; Levine LS; New MI; Pang S; Duchon M; Owens RP; Merkatz IR; Nitowsky BM; Sachs G; Dupont B
    Lancet; 1979 May; 1(8126):1107-8. PubMed ID: 86832
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.