These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 20978868)

  • 1. Metabolic disorders in newly diagnosed young adult female patients with simple virilizing 21-hydroxylase deficiency.
    Zhang HJ; Yang J; Zhang MN; Liu CQ; Xu M; Li XJ; Yang SY; Li XY
    Endocrine; 2010 Oct; 38(2):260-5. PubMed ID: 20978868
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Growth pattern of untreated boys with simple virilizing congenital adrenal hyperplasia indicates relative androgen insensitivity during the first six months of life.
    Bonfig W; Schwarz HP
    Horm Res Paediatr; 2011; 75(4):264-8. PubMed ID: 21196707
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Relationship between adipokines and androgens in children and young adults with congenital adrenal hyperplasia.
    Apsan J; Lekarev O; Thomas C; Zhu YS; Cohan K; Lin-Su K
    Front Endocrinol (Lausanne); 2024; 15():1433378. PubMed ID: 39175574
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hyperinsulinemia and insulin insensitivity in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the relationship between serum leptin levels and chronic hyperinsulinemia.
    Saygili F; Oge A; Yilmaz C
    Horm Res; 2005; 63(6):270-4. PubMed ID: 15956788
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: potential clinical implications.
    Charmandari E; Weise M; Bornstein SR; Eisenhofer G; Keil MF; Chrousos GP; Merke DP
    J Clin Endocrinol Metab; 2002 May; 87(5):2114-20. PubMed ID: 11994350
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adiponectin levels are high in children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency.
    Völkl TM; Simm D; Körner A; Kiess W; Kratzsch J; Dörr HG
    Acta Paediatr; 2009 May; 98(5):885-91. PubMed ID: 19236311
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Salt wasting in simple virilizing congenital adrenal hyperplasia.
    Frisch H; Battelino T; Schober E; Baumgartner-Parzer S; Nowotny P; Vierhapper H
    J Pediatr Endocrinol Metab; 2001; 14(9):1649-55. PubMed ID: 11795656
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Does an altered leptin axis play a role in obesity among children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency?
    Völkl TM; Simm D; Körner A; Rascher W; Kiess W; Kratzsch J; Dörr HG
    Eur J Endocrinol; 2009 Feb; 160(2):239-47. PubMed ID: 19004982
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study.
    Falhammar H; Frisén L; Hirschberg AL; Norrby C; Almqvist C; Nordenskjöld A; Nordenström A
    J Clin Endocrinol Metab; 2015 Sep; 100(9):3520-8. PubMed ID: 26126207
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Influence of Genotype and Hyperandrogenism on Sexual Function in Women With Congenital Adrenal Hyperplasia.
    Schernthaner-Reiter MH; Baumgartner-Parzer S; Egarter HC; Krebs M; Kautzky-Willer A; Kirchheiner K; Luger A; Bayerle-Eder M
    J Sex Med; 2019 Oct; 16(10):1529-1540. PubMed ID: 31447379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and functional characterization of a novel mutation P459H and a rare mutation R483W in the CYP21A2 gene in two Chinese patients with simple virilizing form of congenital adrenal hyperplasia.
    Jiang L; Song LL; Wang H; Wang JL; Wang PP; Zhou HB; Zhang XL
    J Endocrinol Invest; 2012 May; 35(5):485-9. PubMed ID: 21750395
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family.
    Kocova M; Anastasovska V; Bitovska I
    Eur J Med Res; 2019 Jun; 24(1):21. PubMed ID: 31217034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance.
    Khattab A; Yuen T; Al-Malki S; Yau M; Kazmi D; Sun L; Harbison M; Haider S; Zaidi M; New MI
    Ann N Y Acad Sci; 2016 Jan; 1364(1):5-10. PubMed ID: 26291314
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Coeli-Lacchini FB; Turatti W; Elias PC; Elias LL; Martinelli CE; Moreira AC; Antonini SR; de Castro M
    Gene; 2013 Sep; 526(2):239-45. PubMed ID: 23570880
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cardiometabolic Health in Adolescents and Young Adults with Congenital Adrenal Hyperplasia.
    Navardauskaite R; Semeniene K; Sukys M; Pridotkaite A; Vanckaviciene A; Zilaitiene B; Verkauskiene R
    Medicina (Kaunas); 2022 Mar; 58(4):. PubMed ID: 35454339
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cardiovascular risk, metabolic profile, and body composition in adult males with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Falhammar H; Filipsson Nyström H; Wedell A; Thorén M
    Eur J Endocrinol; 2011 Feb; 164(2):285-93. PubMed ID: 21098686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical presentation and mutational spectrum in a series of 166 patients with classical 21-hydroxylase deficiency from South China.
    Su L; Yin X; Cheng J; Cai Y; Wu D; Feng Z; Liu L
    Clin Chim Acta; 2018 Nov; 486():142-150. PubMed ID: 30048636
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Metabolic evaluation of young women with congenital adrenal hyperplasia.
    Schnaider-Rezek GS; Lemos-Marini SH; Baptista MT; Guerra-Júnior G; Morcillo AM; Mello MP; Oliveira LC; D'Souza-Li L
    Arq Bras Endocrinol Metabol; 2011 Nov; 55(8):646-52. PubMed ID: 22218449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variations in the promoter of CYP21A2 gene identified in a Chinese patient with simple virilizing form of 21-hydroxylase deficiency.
    Zhang HJ; Yang J; Zhang MN; Zhang W; Liu JM; Wang WQ; Ning G; Li XY
    Clin Endocrinol (Oxf); 2009 Feb; 70(2):201-7. PubMed ID: 18702679
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency - management in adults.
    Ambroziak U; Bednarczuk T; Ginalska-Malinowska M; Małunowicz EM; Grzechocińska B; Kamiński P; Bablok L; Przedlacki J; Bar-Andziak E
    Endokrynol Pol; 2010; 61(1):142-55. PubMed ID: 20205117
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.