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Journal Abstract Search

1354 related items for PubMed ID: 11694676

  • 1. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
    Gunay-Aygun M, Schwartz S, Heeger S, O'Riordan MA, Cassidy SB.
    Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
    [Abstract] [Full Text] [Related]

  • 2.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Driscoll DJ, Miller JL, Cassidy SB.
    ; 1993 Nov. PubMed ID: 20301505
    [Abstract] [Full Text] [Related]

  • 3. Molecular diagnosis of Prader-Willi syndrome.
    Pangkanon S.
    J Med Assoc Thai; 2003 Aug; 86 Suppl 3():S510-6. PubMed ID: 14700141
    [Abstract] [Full Text] [Related]

  • 4. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
    Angulo MA, Butler MG, Cataletto ME.
    J Endocrinol Invest; 2015 Dec; 38(12):1249-63. PubMed ID: 26062517
    [Abstract] [Full Text] [Related]

  • 5. The behavioral impact of growth hormone treatment for children and adolescents with Prader-Willi syndrome: a 2-year, controlled study.
    Whitman BY, Myers S, Carrel A, Allen D.
    Pediatrics; 2002 Feb; 109(2):E35. PubMed ID: 11826245
    [Abstract] [Full Text] [Related]

  • 6. Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
    Butler MG, Miller JL, Forster JL.
    Curr Pediatr Rev; 2019 Feb; 15(4):207-244. PubMed ID: 31333129
    [Abstract] [Full Text] [Related]

  • 7. Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.
    Butler MG, Manzardo AM, Forster JL.
    Curr Pediatr Rev; 2016 Feb; 12(2):136-66. PubMed ID: 26592417
    [Abstract] [Full Text] [Related]

  • 8. 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; 167A(11):2720-6. PubMed ID: 26109092
    [Abstract] [Full Text] [Related]

  • 9. Clinical and genetic analysis for four Chinese families with Prader-Willi syndrome.
    Zhang YW, Jia HY, Hong J, Ge Y, Zhang HJ, Shen CF, Ye L, Cui B, Li XY, Gu WQ, Zhang YF, Wang WQ, Ning G.
    Endocrine; 2009 Aug; 36(1):37-44. PubMed ID: 19421899
    [Abstract] [Full Text] [Related]

  • 10. [Prader Willi syndrome patients: study of 77 patients].
    Poyatos D, Camprubí C, Gabau E, Nosas R, Villatoro S, Coll MD, Guitart M.
    Med Clin (Barc); 2009 Nov 07; 133(17):649-56. PubMed ID: 19748638
    [Abstract] [Full Text] [Related]

  • 11. Prader-Willi syndrome.
    Cassidy SB, Schwartz S, Miller JL, Driscoll DJ.
    Genet Med; 2012 Jan 07; 14(1):10-26. PubMed ID: 22237428
    [Abstract] [Full Text] [Related]

  • 12. Prader-Willi syndrome.
    Cassidy SB, Driscoll DJ.
    Eur J Hum Genet; 2009 Jan 07; 17(1):3-13. PubMed ID: 18781185
    [Abstract] [Full Text] [Related]

  • 13.
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  • 14. Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.
    Gunay-Aygun M, Heeger S, Schwartz S, Cassidy SB.
    Am J Med Genet; 1997 Jul 11; 71(1):106-10. PubMed ID: 9215778
    [Abstract] [Full Text] [Related]

  • 15.
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  • 16. Referral diagnosis of Prader-Willi syndrome and Angelman syndrome based on methylation-specific polymerase chain reaction.
    Teng YN, Tsai WH, Wu CJ, Lin SJ, Chen YJ, Kuo PL.
    J Formos Med Assoc; 2002 Jul 11; 101(7):488-94. PubMed ID: 12353341
    [Abstract] [Full Text] [Related]

  • 17. Neonatal presentation of Prader Willi sindrome. Personal records.
    Maggio MC, Corsello M, Piccione M, Piro E, Giuffrè M, Liotta A.
    Minerva Pediatr; 2007 Dec 11; 59(6):817-23. PubMed ID: 17978792
    [Abstract] [Full Text] [Related]

  • 18. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
    Hassan M, Butler MG.
    Eur J Med Genet; 2016 Nov 11; 59(11):584-589. PubMed ID: 27659713
    [Abstract] [Full Text] [Related]

  • 19.
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  • 20. [Neonatal presentation of Prader-Willi syndrome: A report of five cases].
    Richard-De Ceaurriz B, Leymarie C, Godefroy A, Collignon P, Sigaudy S, Truc P.
    Arch Pediatr; 2017 Nov 11; 24(11):1115-1120. PubMed ID: 28967604
    [Abstract] [Full Text] [Related]

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