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Journal Abstract Search

678 related items for PubMed ID: 17625998

  • 21. Voiding dysfunction and the Williams-Beuren syndrome: a clinical and urodynamic investigation.
    Sammour ZM, Gomes CM, Duarte RJ, Trigo-Rocha FE, Srougi M.
    J Urol; 2006 Apr; 175(4):1472-6. PubMed ID: 16516025
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  • 23. [Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype].
    Battin J, Lacombe D, Taine L, Goizet C.
    Bull Acad Natl Med; 2000 Apr; 184(1):105-15; discussion 115-6. PubMed ID: 10989534
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  • 24. Williams syndrome and the elastin gene in Thai patients.
    Ruangdaraganon N, Tocharoentanaphol C, Kotchabhakdi N, Khowsathit P.
    J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S174-8. PubMed ID: 10730539
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  • 28. [Cardiovascular manifestations in 40 patients with Williams syndrome].
    Xie CH, Zhao ZY, Yang JB, Qin YF, Shao J, Gong FQ.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2007 Oct; 35(10):904-7. PubMed ID: 18206036
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  • 29. Diagnosis and management of medical problems in adults with Williams-Beuren syndrome.
    Pober BR, Morris CA.
    Am J Med Genet C Semin Med Genet; 2007 Aug 15; 145C(3):280-90. PubMed ID: 17639596
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  • 30. [Clinical features of a senior patient with Williams syndrome].
    Nakaji A, Kawame Y, Nagai C, Iwata M.
    Rinsho Shinkeigaku; 2001 Sep 15; 41(9):592-8. PubMed ID: 11968743
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  • 31. [Clinical aspects and genetics of Williams-Beuren syndrome. Clinical and molecular genetic study of 44 patients with suspected Williams-Beuren syndrome].
    von Beust G, Laccone FA, del Pilar Andrino M, Wessel A.
    Klin Padiatr; 2000 Sep 15; 212(6):299-307. PubMed ID: 11190824
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  • 33. [Extended aortoplasty for supravalvular aortic stenosis with Williams syndrome].
    Nagasaka S, Taniguchi S, Kawata T, Mizuguchi K, Kawachi K, Kitamura S.
    Nihon Kyobu Geka Gakkai Zasshi; 1997 Apr 15; 45(4):601-6. PubMed ID: 9155132
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  • 38. Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome.
    Leme DE, Souza DH, Mercado G, Pastene E, Dias A, Moretti-Ferreira D.
    Genet Mol Res; 2013 Sep 04; 12(3):3407-11. PubMed ID: 24065682
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  • 39. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.
    Ewart AK, Morris CA, Atkinson D, Jin W, Sternes K, Spallone P, Stock AD, Leppert M, Keating MT.
    Nat Genet; 1993 Sep 04; 5(1):11-6. PubMed ID: 7693128
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