BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 11232002)

  • 1. Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Deneux C; Tardy V; Dib A; Mornet E; Billaud L; Charron D; Morel Y; Kuttenn F
    J Clin Endocrinol Metab; 2001 Jan; 86(1):207-13. PubMed ID: 11232002
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A multicenter study of women with nonclassical congenital adrenal hyperplasia: relationship between genotype and phenotype.
    Speiser PW; Knochenhauer ES; Dewailly D; Fruzzetti F; Marcondes JA; Azziz R
    Mol Genet Metab; 2000 Nov; 71(3):527-34. PubMed ID: 11073721
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.
    Bidet M; Bellanné-Chantelot C; Galand-Portier MB; Tardy V; Billaud L; Laborde K; Coussieu C; Morel Y; Vaury C; Golmard JL; Claustre A; Mornet E; Chakhtoura Z; Mowszowicz I; Bachelot A; Touraine P; Kuttenn F
    J Clin Endocrinol Metab; 2009 May; 94(5):1570-8. PubMed ID: 19208730
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hyperandrogenism in carriers of CYP21 mutations: the role of genotype.
    Admoni O; Israel S; Lavi I; Gur M; Tenenbaum-Rakover Y
    Clin Endocrinol (Oxf); 2006 Jun; 64(6):645-51. PubMed ID: 16712666
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.
    Dolzan V; Sólyom J; Fekete G; Kovács J; Rakosnikova V; Votava F; Lebl J; Pribilincova Z; Baumgartner-Parzer SM; Riedl S; Waldhauser F; Frisch H; Stopar-Obreza M; Krzisnik C; Battelino T
    Eur J Endocrinol; 2005 Jul; 153(1):99-106. PubMed ID: 15994751
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Bachega TA; Billerbeck AE; Marcondes JA; Madureira G; Arnhold IJ; Mendonca BB
    Clin Endocrinol (Oxf); 2000 May; 52(5):601-7. PubMed ID: 10792340
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.
    Speiser PW; New MI
    J Clin Endocrinol Metab; 1987 Jan; 64(1):86-91. PubMed ID: 3023431
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations.
    Escobar-Morreale HF; San Millán JL; Smith RR; Sancho J; Witchel SF
    Fertil Steril; 1999 Oct; 72(4):629-38. PubMed ID: 10521100
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype analysis in late onset 21-hydroxylase deficiency in comparison to the classical forms.
    Rumsby G; Avey CJ; Conway GS; Honour JW
    Clin Endocrinol (Oxf); 1998 Jun; 48(6):707-11. PubMed ID: 9713558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients.
    Dain LB; Buzzalino ND; Oneto A; Belli S; Stivel M; Pasqualini T; Minutolo C; Charreau EH; Alba LG
    Clin Endocrinol (Oxf); 2002 Feb; 56(2):239-45. PubMed ID: 11874416
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations.
    Stikkelbroeck NM; Hoefsloot LH; de Wijs IJ; Otten BJ; Hermus AR; Sistermans EA
    J Clin Endocrinol Metab; 2003 Aug; 88(8):3852-9. PubMed ID: 12915679
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.
    Krone N; Braun A; Roscher AA; Knorr D; Schwarz HP
    J Clin Endocrinol Metab; 2000 Mar; 85(3):1059-65. PubMed ID: 10720040
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.
    Weintrob N; Brautbar C; Pertzelan A; Josefsberg Z; Dickerman Z; Kauschansky A; Lilos P; Peled D; Phillip M; Israel S
    Eur J Endocrinol; 2000 Sep; 143(3):397-403. PubMed ID: 11022183
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The spectrum of molecular defects of the CYP21 gene in the Hellenic population: variable concordance between genotype and phenotype in the different forms of congenital adrenal hyperplasia.
    Dracopoulou-Vabouli M; Maniati-Christidi M; Dacou-Voutetakis C
    J Clin Endocrinol Metab; 2001 Jun; 86(6):2845-8. PubMed ID: 11397897
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.
    Tardy V; Menassa R; Sulmont V; Lienhardt-Roussie A; Lecointre C; Brauner R; David M; Morel Y
    J Clin Endocrinol Metab; 2010 Mar; 95(3):1288-300. PubMed ID: 20080860
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency.
    Porzio O; Cunsolo V; Malaponti M; De Nisco E; Acquafredda A; Cavallo L; Andreani M; Giardina E; Testi M; Cappa M; Federici G
    J Clin Endocrinol Metab; 2006 Nov; 91(11):4510-3. PubMed ID: 16912133
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylase.
    Delague V; Souraty N; Khallouf E; Tardy V; Chouery E; Halaby G; Loiselet J; Morel Y; Mégarbané A
    Horm Res; 2000; 53(2):77-82. PubMed ID: 10971093
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia.
    Torres N; Mello MP; Germano CM; Elias LL; Moreira AC; Castro M
    Braz J Med Biol Res; 2003 Oct; 36(10):1311-8. PubMed ID: 14502362
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in northeastern Iran.
    Vakili R; Baradaran-Heravi A; Barid-Fatehi B; Gholamin M; Ghaemi N; Abbaszadegan MR
    Horm Res; 2005; 63(3):119-24. PubMed ID: 15775714
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CYP21 analysis and phenotype/genotype relationship in the screened population of the Italian Emilia-Romagna region.
    Balsamo A; Cacciari E; Baldazzi L; Tartaglia L; Cassio A; Mantovani V; Piazzi S; Cicognani A; Pirazzoli P; Mainetti B; Zappulla F
    Clin Endocrinol (Oxf); 2000 Jul; 53(1):117-25. PubMed ID: 10931088
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.