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PUBMED FOR HANDHELDS

Journal Abstract Search

267 related items for PubMed ID: 23337011

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  • 2. Intractable apnoeic seizures in a child with a deletion typically associated with Williams syndrome.
    Jan S, Ochi A, Kagawa K, Gill P, Guttmann A, Otsubo H, Kobayashi J.
    Epileptic Disord; 2018 Dec 01; 20(6):530-534. PubMed ID: 30530430
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  • 3. Recurrent achalasia in a child with Williams-Beuren syndrome.
    Pereza N, Barbarić I, Ostojić S, Cace N, Kapović M.
    Coll Antropol; 2011 Sep 01; 35(3):941-4. PubMed ID: 22053584
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  • 7. Multiple causes of apnea in 1p36 deletion syndrome include seizures.
    Kanabar G, Boyd S, Schugal A, Bhate S.
    Seizure; 2012 Jun 01; 21(5):402-6. PubMed ID: 22425009
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  • 8. Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.
    Nicita F, Garone G, Spalice A, Savasta S, Striano P, Pantaleoni C, Spartà MV, Kluger G, Capovilla G, Pruna D, Freri E, D'Arrigo S, Verrotti A.
    Am J Med Genet A; 2016 Jan 01; 170A(1):148-55. PubMed ID: 26437767
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  • 9. Williams-Beuren Syndrome: more or less? Segmental duplications and deletions in the Williams-Beuren syndrome region provide new insights into language development.
    Tassabehji M, Donnai D.
    Eur J Hum Genet; 2006 May 01; 14(5):507-8. PubMed ID: 16523213
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  • 11. Clinical expression of familial Williams-Beuren syndrome in a Turkish family.
    Parlak M, Nur BG, Mıhçı E, Durmaz E, Karaüzüm SB, Akcurin S, Bircan İ.
    J Pediatr Endocrinol Metab; 2014 Jan 01; 27(1-2):153-8. PubMed ID: 24057591
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  • 13. [Syndromes 5. Williams-Beuren Syndrome].
    Hoff M, van Hagen JM, Baart JA, Vissink A.
    Ned Tijdschr Tandheelkd; 1998 Oct 01; 105(10):368-9. PubMed ID: 11928452
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  • 19. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome].
    Milà M, Carrió A, Sánchez A, Gómez D, Jiménez D, Estivill X, Ballesta F.
    Med Clin (Barc); 1999 Jun 19; 113(2):46-9. PubMed ID: 10425618
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  • 20. Bilateral vocal cord paralysis and hypothyroidism as presenting symptoms of Williams-Beuren syndrome: a case report.
    Koren I, Kessel I, Rotschild A, Cohen-Kerem R.
    Int J Pediatr Otorhinolaryngol; 2015 Sep 19; 79(9):1582-3. PubMed ID: 26143126
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