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PUBMED FOR HANDHELDS

Journal Abstract Search

318 related items for PubMed ID: 33647242

  • 21.
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  • 23. Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.
    Irizarry KA, Miller M, Freemark M, Haqq AM.
    Adv Pediatr; 2016 Aug; 63(1):47-77. PubMed ID: 27426895
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  • 24.
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  • 25. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC, Person RE, Flores A, Villanos MT, Bi W, Wiszniewska J, Bacino CA.
    Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
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  • 26. Evaluation of Prader-Willi Syndrome gene MAGEL2 in severe childhood-onset obesity.
    O'Neill MA, Farooqi IS, Wevrick R.
    Obes Res; 2005 Oct; 13(10):1841-2. PubMed ID: 16286533
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  • 27. Autonomic nervous system dysfunction in Prader-Willi syndrome.
    Butler MG, Victor AK, Reiter LT.
    Clin Auton Res; 2023 Jun; 33(3):281-286. PubMed ID: 36515769
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  • 28. Prader-Willi syndrome and the hypothalamus.
    Swaab DF.
    Acta Paediatr Suppl; 1997 Nov; 423():50-4. PubMed ID: 9401539
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  • 29. Endocrine and metabolic aspects of adult Prader-Willi syndrome with special emphasis on the effect of growth hormone treatment.
    Höybye C.
    Growth Horm IGF Res; 2004 Feb; 14(1):1-15. PubMed ID: 14700552
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  • 32. [Prader-Willi-Labhart syndrome: relations with the hypothalamus and chromosome 15].
    Touraine P, Mbikay M, Seidah NG, Chrétien M.
    Ann Endocrinol (Paris); 1990 Feb; 51(5-6):202-8. PubMed ID: 2130760
    [Abstract] [Full Text] [Related]

  • 33. Endocrine phenotype of 6q16.1-q21 deletion involving SIM1 and Prader-Willi syndrome-like features.
    Izumi K, Housam R, Kapadia C, Stallings VA, Medne L, Shaikh TH, Kublaoui BM, Zackai EH, Grimberg A.
    Am J Med Genet A; 2013 Dec; 161A(12):3137-43. PubMed ID: 24038875
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  • 34.
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  • 35. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K.
    Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
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  • 36. Transcriptomics of the Prader-Willi syndrome hypothalamus.
    Bochukova EG.
    Handb Clin Neurol; 2021 Nov; 181():369-379. PubMed ID: 34238471
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  • 37.
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  • 38. Primary gonadal failure and precocious adrenarche in a boy with Prader-Labhart-Willi syndrome.
    Garty B, Shuper A, Mimouni M, Varsano I, Kauli R.
    Eur J Pediatr; 1982 Nov; 139(3):201-3. PubMed ID: 7160409
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