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Journal Abstract Search

595 related items for PubMed ID: 29525066

  • 1. [Diffuse hypertrichosis revealing non-classical congenital adrenal hyperplasia].
    Berthin C, Sibilia P, Martins-Hericher J, Donzeau A, Martin L.
    Ann Dermatol Venereol; 2018 Apr; 145(4):270-277. PubMed ID: 29525066
    [Abstract] [Full Text] [Related]

  • 2. 17-Hydroxyprogesterone in children, adolescents and adults.
    Honour JW.
    Ann Clin Biochem; 2014 Jul; 51(Pt 4):424-40. PubMed ID: 24711560
    [Abstract] [Full Text] [Related]

  • 3. Clinical and hormonal characteristics in heterozygote carriers of congenital adrenal hyperplasia.
    Guarnotta V, Niceta M, Bono M, Marchese S, Fabiano C, Indelicato S, Di Gaudio F, Garofalo P, Giordano C.
    J Steroid Biochem Mol Biol; 2020 Apr; 198():105554. PubMed ID: 31805392
    [Abstract] [Full Text] [Related]

  • 4. An update of congenital adrenal hyperplasia.
    New MI.
    Ann N Y Acad Sci; 2004 Dec; 1038():14-43. PubMed ID: 15838095
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Oct; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 7. The frequency of CYP 21 gene mutations in Turkish women with hyperandrogenism.
    Kelestimur F, Everest H, Dundar M, Tanriverdi F, White C, Witchel SF.
    Exp Clin Endocrinol Diabetes; 2009 May; 117(5):205-8. PubMed ID: 19085698
    [Abstract] [Full Text] [Related]

  • 8. A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia.
    Kawashima Y, Usui T, Fujimoto M, Miyahara N, Nishimura R, Hanaki K, Kanzaki S.
    Endocr J; 2015 May; 62(1):101-6. PubMed ID: 25319875
    [Abstract] [Full Text] [Related]

  • 9.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, Nimkarn S, Gangishetti PK, Yau M, New MI.
    ; 1993 May. PubMed ID: 20301350
    [Abstract] [Full Text] [Related]

  • 10. The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene.
    Livadas S, Dracopoulou M, Dastamani A, Sertedaki A, Maniati-Christidi M, Magiakou AM, Kanaka-Gantenbein C, Chrousos GP, Dacou-Voutetakis C.
    Clin Endocrinol (Oxf); 2015 Apr; 82(4):543-9. PubMed ID: 25041270
    [Abstract] [Full Text] [Related]

  • 11. The prevalence of non-classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Greek women with hirsutism and polycystic ovary syndrome.
    Trakakis E, Rizos D, Loghis C, Chryssikopoulos A, Spyropoulou M, Salamalekis E, Simeonides G, Vagopoulos V, Salamalekis G, Kassanos D.
    Endocr J; 2008 Mar; 55(1):33-9. PubMed ID: 18187875
    [Abstract] [Full Text] [Related]

  • 12. Simple virilising congenital adrenal hyperplasia in monozygotic twins: A rare report and review of previous cases.
    Muthuvel B, Gautam A, Pal R, Panigrahi I, Dayal D.
    Pediatr Endocrinol Diabetes Metab; 2020 Mar; 26(1):58-62. PubMed ID: 32272826
    [Abstract] [Full Text] [Related]

  • 13. Congenital adrenal hyperplasia clinical characteristics and genotype in newborn, childhood and adolescence.
    Pasqualini T, Alonso G, Tomasini R, Galich AM, Buzzalino N, Fernandez C, Minutolo C, Alba L, Dain L.
    Medicina (B Aires); 2007 Mar; 67(3):253-61. PubMed ID: 17628913
    [Abstract] [Full Text] [Related]

  • 14. Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review.
    Papadakis G, Kandaraki EA, Tseniklidi E, Papalou O, Diamanti-Kandarakis E.
    Front Endocrinol (Lausanne); 2019 Mar; 10():388. PubMed ID: 31275245
    [Abstract] [Full Text] [Related]

  • 15. Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report.
    Cheng T, Liu J, Sun W, Song G, Ma H.
    BMC Endocr Disord; 2022 Mar 07; 22(1):57. PubMed ID: 35255871
    [Abstract] [Full Text] [Related]

  • 16. Unusual phenotype of congenital adrenal hyperplasia (CAH) with a novel mutation of the CYP21A2 gene.
    Raisingani M, Contreras MF, Prasad K, Pappas JG, Kluge ML, Shah B, David R.
    J Pediatr Endocrinol Metab; 2016 Jul 01; 29(7):867-71. PubMed ID: 27180336
    [Abstract] [Full Text] [Related]

  • 17. Intrafamilial Phenotypic Variability and Consequences of Non-Compliance with Treatment in Congenital Adrenal Hyperplasia and Congenital Hypothyroidism within a Single Family
.
    Improda N, Ponmani C, Schoenmakers N, Senniappan S, Atterbury A, Barnicoat A, Chatterjee K, Dattani MT.
    Horm Res Paediatr; 2017 Jul 01; 88(2):172-178. PubMed ID: 28359061
    [Abstract] [Full Text] [Related]

  • 18. A novel mutation in the NR0B1 gene in a family with monozygotic twin sisters and congenital adrenal hypoplasia affected children.
    Minari R, Vottero A, Tassi F, Viani I, Neri TM, Street ME, Ghizzoni L, Bernasconi S, Martorana D.
    Hormones (Athens); 2015 Jul 01; 14(1):160-6. PubMed ID: 25402384
    [Abstract] [Full Text] [Related]

  • 19. Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche.
    Savas Erdeve S, Berberoglu M, Yurur-Kutlay N, Siklar Z, Hacihamdioglu B, Tukun A, Ocal G.
    J Pediatr Endocrinol Metab; 2011 Jul 01; 24(11-12):965-70. PubMed ID: 22308849
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

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