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257 related items for PubMed ID: 25532039

  • 1. Gene expression patterns in relation to the clinical phenotype in Klinefelter syndrome.
    Zitzmann M, Bongers R, Werler S, Bogdanova N, Wistuba J, Kliesch S, Gromoll J, Tüttelmann F.
    J Clin Endocrinol Metab; 2015 Mar; 100(3):E518-23. PubMed ID: 25532039
    [Abstract] [Full Text] [Related]

  • 2. Anthropometry in Klinefelter syndrome--multifactorial influences due to CAG length, testosterone treatment and possibly intrauterine hypogonadism.
    Chang S, Skakkebæk A, Trolle C, Bojesen A, Hertz JM, Cohen A, Hougaard DM, Wallentin M, Pedersen AD, Østergaard JR, Gravholt CH.
    J Clin Endocrinol Metab; 2015 Mar; 100(3):E508-17. PubMed ID: 25514102
    [Abstract] [Full Text] [Related]

  • 3. Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome.
    Wikström AM, Painter JN, Raivio T, Aittomäki K, Dunkel L.
    Clin Endocrinol (Oxf); 2006 Jul; 65(1):92-7. PubMed ID: 16817826
    [Abstract] [Full Text] [Related]

  • 4. Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.
    Zinn AR, Ramos P, Elder FF, Kowal K, Samango-Sprouse C, Ross JL.
    J Clin Endocrinol Metab; 2005 Sep; 90(9):5041-6. PubMed ID: 15956082
    [Abstract] [Full Text] [Related]

  • 5. The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype.
    Rocca MS, Pecile V, Cleva L, Speltra E, Selice R, Di Mambro A, Foresta C, Ferlin A.
    Andrology; 2016 Mar; 4(2):328-34. PubMed ID: 26789125
    [Abstract] [Full Text] [Related]

  • 6. Clinical, endocrinological, and epigenetic features of the 46,XX male syndrome, compared with 47,XXY Klinefelter patients.
    Vorona E, Zitzmann M, Gromoll J, Schüring AN, Nieschlag E.
    J Clin Endocrinol Metab; 2007 Sep; 92(9):3458-65. PubMed ID: 17579198
    [Abstract] [Full Text] [Related]

  • 7. Bone mass in subjects with Klinefelter syndrome: role of testosterone levels and androgen receptor gene CAG polymorphism.
    Ferlin A, Schipilliti M, Vinanzi C, Garolla A, Di Mambro A, Selice R, Lenzi A, Foresta C.
    J Clin Endocrinol Metab; 2011 Apr; 96(4):E739-45. PubMed ID: 21270324
    [Abstract] [Full Text] [Related]

  • 8. Neuropsychology and brain morphology in Klinefelter syndrome - the impact of genetics.
    Skakkebaek A, Bojesen A, Kristensen MK, Cohen A, Hougaard DM, Hertz JM, Fedder J, Laurberg P, Wallentin M, Østergaard JR, Pedersen AD, Gravholt CH.
    Andrology; 2014 Jul; 2(4):632-40. PubMed ID: 24865607
    [Abstract] [Full Text] [Related]

  • 9. Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome.
    Poplinski A, Wieacker P, Kliesch S, Gromoll J.
    Eur J Endocrinol; 2010 Jan; 162(1):169-75. PubMed ID: 19812237
    [Abstract] [Full Text] [Related]

  • 10. Is there an influence of X-chromosomal imprinting on the phenotype in Klinefelter syndrome? A clinical and molecular genetic study of 61 cases.
    Stemkens D, Roza T, Verrij L, Swaab H, van Werkhoven MK, Alizadeh BZ, Sinke RJ, Giltay JC.
    Clin Genet; 2006 Jul; 70(1):43-8. PubMed ID: 16813603
    [Abstract] [Full Text] [Related]

  • 11. Novel genetic aspects of Klinefelter's syndrome.
    Tüttelmann F, Gromoll J.
    Mol Hum Reprod; 2010 Jun; 16(6):386-95. PubMed ID: 20228051
    [Abstract] [Full Text] [Related]

  • 12. New approaches to the Klinefelter syndrome.
    Nieschlag E, Werler S, Wistuba J, Zitzmann M.
    Ann Endocrinol (Paris); 2014 May; 75(2):88-97. PubMed ID: 24793990
    [Abstract] [Full Text] [Related]

  • 13. Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome.
    Zitzmann M, Rohayem J.
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):302-312. PubMed ID: 32415901
    [Abstract] [Full Text] [Related]

  • 14. Chromosomal variants in klinefelter syndrome.
    Frühmesser A, Kotzot D.
    Sex Dev; 2011 Jun; 5(3):109-23. PubMed ID: 21540567
    [Abstract] [Full Text] [Related]

  • 15. Methylation-specific PCR allows for fast diagnosis of X chromosome disomy and reveals skewed inactivation of the X chromosome in men with Klinefelter syndrome.
    Mehta A, Malek-Jones M, Bolyakov A, Mielnik A, Schlegel PN, Paduch DA.
    J Androl; 2012 Jun; 33(5):955-62. PubMed ID: 22441764
    [Abstract] [Full Text] [Related]

  • 16. Insights into the pathogenesis of XXY phenotype from comparison of the clinical syndrome with an experimental XXY mouse model.
    Lue YH, Wang C, Liu PY, Erkilla K, Swerdloff RS.
    Pediatr Endocrinol Rev; 2010 Dec; 8 Suppl 1():140-4. PubMed ID: 21217605
    [Abstract] [Full Text] [Related]

  • 17. The parent-of-origin of the extra X chromosome may differentially affect psychopathology in Klinefelter syndrome.
    Bruining H, van Rijn S, Swaab H, Giltay J, Kates W, Kas MJ, van Engeland H, de Sonneville L.
    Biol Psychiatry; 2010 Dec 15; 68(12):1156-62. PubMed ID: 21035791
    [Abstract] [Full Text] [Related]

  • 18. Genotype and phenotype in Klinefelter syndrome - impact of androgen receptor polymorphism and skewed X inactivation.
    Bojesen A, Hertz JM, Gravholt CH.
    Int J Androl; 2011 Dec 15; 34(6 Pt 2):e642-8. PubMed ID: 21977989
    [Abstract] [Full Text] [Related]

  • 19. Human induced pluripotent stem cells from two azoospermic patients with Klinefelter syndrome show similar X chromosome inactivation behavior to female pluripotent stem cells.
    Panula S, Kurek M, Kumar P, Albalushi H, Padrell Sánchez S, Damdimopoulou P, Olofsson JI, Hovatta O, Lanner F, Stukenborg JB.
    Hum Reprod; 2019 Nov 01; 34(11):2297-2310. PubMed ID: 31743397
    [Abstract] [Full Text] [Related]

  • 20. In search for significant cognitive features in Klinefelter syndrome through cross-species comparison of a supernumerary X chromosome.
    Bruining H, Swaab H, de Sonneville LM, van Rijn S, van Engeland H, Kas MJ.
    Genes Brain Behav; 2011 Aug 01; 10(6):658-62. PubMed ID: 21605339
    [Abstract] [Full Text] [Related]

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