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PUBMED FOR HANDHELDS

Journal Abstract Search


188 related items for PubMed ID: 18422527

  • 1. 'Hungry Eyes': visual processing of food images in adults with Prader-Willi syndrome.
    Key AP, Dykens EM.
    J Intellect Disabil Res; 2008 Jun; 52(Pt 6):536-46. PubMed ID: 18422527
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  • 4. Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome.
    Coupaye M, Tauber M, Cuisset L, Laurier V, Bieth E, Lacorte JM, Oppert JM, Clément K, Poitou C.
    J Clin Endocrinol Metab; 2016 Dec; 101(12):4895-4903. PubMed ID: 27662437
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  • 6. A review of chemosensory perceptions, food preferences and food-related behaviours in subjects with Prader-Willi Syndrome.
    Martínez Michel L, Haqq AM, Wismer WV.
    Appetite; 2016 Apr 01; 99():17-24. PubMed ID: 26713776
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  • 7. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.
    Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T.
    Pediatrics; 2004 Mar 01; 113(3 Pt 1):565-73. PubMed ID: 14993551
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  • 8. Importance of reward and prefrontal circuitry in hunger and satiety: Prader-Willi syndrome vs simple obesity.
    Holsen LM, Savage CR, Martin LE, Bruce AS, Lepping RJ, Ko E, Brooks WM, Butler MG, Zarcone JR, Goldstein JM.
    Int J Obes (Lond); 2012 May 01; 36(5):638-47. PubMed ID: 22024642
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  • 9. A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
    Morandi A, Bonnefond A, Lobbens S, Carotenuto M, Del Giudice EM, Froguel P, Maffeis C.
    Am J Med Genet A; 2015 Nov 01; 167A(11):2720-6. PubMed ID: 26109092
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  • 11. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.
    Muthusamy K, Macke EL, Klee EW, Tebben PJ, Hand JL, Hasadsri L, Marcou CA, Schimmenti LA.
    Am J Med Genet A; 2020 Oct 01; 182(10):2442-2449. PubMed ID: 32815268
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  • 14. Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences.
    Dimitropoulos A, Ferranti A, Lemler M.
    J Commun Disord; 2013 Oct 01; 46(2):193-201. PubMed ID: 23295077
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  • 15. Metabolic syndrome in adult patients with Prader-Willi syndrome.
    Grugni G, Crinò A, Bedogni G, Cappa M, Sartorio A, Corrias A, Di Candia S, Gargantini L, Iughetti L, Pagano C, Ragusa L, Salvatoni A, Spera S, Vettor R, Chiumello G, Brambilla P.
    Nutr Metab Cardiovasc Dis; 2013 Nov 01; 23(11):1134-40. PubMed ID: 23220075
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  • 16. Neural mechanisms underlying hyperphagia in Prader-Willi syndrome.
    Holsen LM, Zarcone JR, Brooks WM, Butler MG, Thompson TI, Ahluwalia JS, Nollen NL, Savage CR.
    Obesity (Silver Spring); 2006 Jun 01; 14(6):1028-37. PubMed ID: 16861608
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  • 18. Deconvolution-based assessment of pituitary GH secretion stimulated with GHRH+arginine in Prader-Willi adults and obese controls.
    Grugni G, Marostica E, Crinò A, Marzullo P, De Nicolao G, Sartorio A.
    Clin Endocrinol (Oxf); 2013 Aug 01; 79(2):224-31. PubMed ID: 23301953
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  • 19. The neuroanatomy of genetic subtype differences in Prader-Willi syndrome.
    Honea RA, Holsen LM, Lepping RJ, Perea R, Butler MG, Brooks WM, Savage CR.
    Am J Med Genet B Neuropsychiatr Genet; 2012 Mar 01; 159B(2):243-53. PubMed ID: 22241551
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  • 20. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
    Bittel DC, Kibiryeva N, Butler MG.
    Pediatrics; 2006 Oct 01; 118(4):e1276-83. PubMed ID: 16982806
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