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Journal Abstract Search

335 related items for PubMed ID: 25279502

  • 1. Increased mortality in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Falhammar H, Frisén L, Norrby C, Hirschberg AL, Almqvist C, Nordenskjöld A, Nordenström A.
    J Clin Endocrinol Metab; 2014 Dec; 99(12):E2715-21. PubMed ID: 25279502
    [Abstract] [Full Text] [Related]

  • 2. Increased psychiatric morbidity in men with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Falhammar H, Butwicka A, Landén M, Lichtenstein P, Nordenskjöld A, Nordenström A, Frisén L.
    J Clin Endocrinol Metab; 2014 Mar; 99(3):E554-60. PubMed ID: 24302749
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Congenital adrenal hyperplasia and risk for psychiatric disorders in girls and women born between 1915 and 2010: A total population study.
    Engberg H, Butwicka A, Nordenström A, Hirschberg AL, Falhammar H, Lichtenstein P, Nordenskjöld A, Frisén L, Landén M.
    Psychoneuroendocrinology; 2015 Oct; 60():195-205. PubMed ID: 26184920
    [Abstract] [Full Text] [Related]

  • 5. No evidence of an increase in early infant mortality from congenital adrenal hyperplasia in the absence of screening.
    Hird BE, Tetlow L, Tobi S, Patel L, Clayton PE.
    Arch Dis Child; 2014 Feb; 99(2):158-64. PubMed ID: 24225272
    [Abstract] [Full Text] [Related]

  • 6. Suboptimal psychosocial outcomes in patients with congenital adrenal hyperplasia: epidemiological studies in a nonbiased national cohort in Sweden.
    Strandqvist A, Falhammar H, Lichtenstein P, Hirschberg AL, Wedell A, Norrby C, Nordenskjöld A, Frisén L, Nordenström A.
    J Clin Endocrinol Metab; 2014 Apr; 99(4):1425-32. PubMed ID: 24476073
    [Abstract] [Full Text] [Related]

  • 7. Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany.
    Dörr HG, Wollmann HA, Hauffa BP, Woelfle J, German Society of Pediatric Endocrinology and Diabetology.
    BMC Endocr Disord; 2018 Jun 08; 18(1):37. PubMed ID: 29884168
    [Abstract] [Full Text] [Related]

  • 8. Increased Prevalence of Fractures in Congenital Adrenal Hyperplasia: A Swedish Population-based National Cohort Study.
    Falhammar H, Frisén L, Hirschberg AL, Nordenskjöld A, Almqvist C, Nordenström A.
    J Clin Endocrinol Metab; 2022 Jan 18; 107(2):e475-e486. PubMed ID: 34601607
    [Abstract] [Full Text] [Related]

  • 9. One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study.
    Gidlöf S, Falhammar H, Thilén A, von Döbeln U, Ritzén M, Wedell A, Nordenström A.
    Lancet Diabetes Endocrinol; 2013 Sep 18; 1(1):35-42. PubMed ID: 24622265
    [Abstract] [Full Text] [Related]

  • 10. Nationwide neonatal screening for congenital adrenal hyperplasia in sweden: a 26-year longitudinal prospective population-based study.
    Gidlöf S, Wedell A, Guthenberg C, von Döbeln U, Nordenström A.
    JAMA Pediatr; 2014 Jun 18; 168(6):567-74. PubMed ID: 24733564
    [Abstract] [Full Text] [Related]

  • 11. Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in croatia between 1995 and 2006.
    Dumic K, Krnic N, Skrabic V, Stipancic G, Cvijovic K, Kusec V, Stingl K.
    Horm Res; 2009 Jun 18; 72(5):310-4. PubMed ID: 19844117
    [Abstract] [Full Text] [Related]

  • 12. Carriers of a Classic CYP21A2 Mutation Have Reduced Mortality: A Population-Based National Cohort Study.
    Nordenström A, Svensson J, Lajic S, Frisén L, Nordenskjöld A, Norrby C, Almqvist C, Falhammar H.
    J Clin Endocrinol Metab; 2019 Dec 01; 104(12):6148-6154. PubMed ID: 31393570
    [Abstract] [Full Text] [Related]

  • 13. Increased Prevalence of Accidents and Injuries in Congenital Adrenal Hyperplasia: A Population-based Cohort Study.
    Falhammar H, Hirschberg AL, Nordenskjöld A, Larsson H, Nordenström A.
    J Clin Endocrinol Metab; 2024 Feb 20; 109(3):e1175-e1184. PubMed ID: 37862468
    [Abstract] [Full Text] [Related]

  • 14. How many deaths can be prevented by newborn screening for congenital adrenal hyperplasia?
    Grosse SD, Van Vliet G.
    Horm Res; 2007 Feb 20; 67(6):284-91. PubMed ID: 17199092
    [Abstract] [Full Text] [Related]

  • 15. Presenting status of children with classical congenital adrenal hyperplasia over two decades (1999-2018) in the absence of newborn screening in Sri Lanka.
    Seneviratne SN, Sandakelum U, Jayawardena CH, Weerasinghe AM, Wickramarachchi PS, de Silva S.
    J Pediatr Endocrinol Metab; 2021 Sep 27; 34(9):1131-1137. PubMed ID: 34192833
    [Abstract] [Full Text] [Related]

  • 16. Reduced Frequency of Biological and Increased Frequency of Adopted Children in Males With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study.
    Falhammar H, Frisén L, Norrby C, Almqvist C, Hirschberg AL, Nordenskjöld A, Nordenström A.
    J Clin Endocrinol Metab; 2017 Nov 01; 102(11):4191-4199. PubMed ID: 28945916
    [Abstract] [Full Text] [Related]

  • 17. Ethnic and gender differences in rates of congenital adrenal hyperplasia in Western Australia over a 21 year period.
    Shetty VB, Bower C, Jones TW, Lewis BD, Davis EA.
    J Paediatr Child Health; 2012 Nov 01; 48(11):1029-32. PubMed ID: 23039988
    [Abstract] [Full Text] [Related]

  • 18. Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia.
    Morissette R, Chen W, Perritt AF, Dreiling JL, Arai AE, Sachdev V, Hannoush H, Mallappa A, Xu Z, McDonnell NB, Quezado M, Merke DP.
    J Clin Endocrinol Metab; 2015 Aug 01; 100(8):E1143-52. PubMed ID: 26075496
    [Abstract] [Full Text] [Related]

  • 19. Reproductive and Perinatal Outcomes in Women with Congenital Adrenal Hyperplasia: A Population-based Cohort Study.
    Hirschberg AL, Gidlöf S, Falhammar H, Frisén L, Almqvist C, Nordenskjöld A, Nordenström A.
    J Clin Endocrinol Metab; 2021 Jan 23; 106(2):e957-e965. PubMed ID: 33135723
    [Abstract] [Full Text] [Related]

  • 20. Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency.
    Charmandari E, Eisenhofer G, Mehlinger SL, Carlson A, Wesley R, Keil MF, Chrousos GP, New MI, Merke DP.
    J Clin Endocrinol Metab; 2002 Jul 23; 87(7):3031-7. PubMed ID: 12107196
    [Abstract] [Full Text] [Related]

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