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Journal Abstract Search

113 related items for PubMed ID: 25772942

  • 1. Williams Syndrome with Infantile Spasms.
    Polat İ, Karaoglu P, Ayanoglu M, Yis U, Hiz S.
    Indian J Pediatr; 2015 Aug; 82(8):757-8. PubMed ID: 25772942
    [No Abstract] [Full Text] [Related]

  • 2. Infantile spasms in two children with Williams syndrome.
    Tsao CY, Westman JA.
    Am J Med Genet; 1997 Jul 11; 71(1):54-6. PubMed ID: 9215769
    [Abstract] [Full Text] [Related]

  • 3. Infantile spasms in Williams-Beuren syndrome with typical deletions of the 7q11.23 critical region and a review of the literature.
    Samanta D.
    Acta Neurol Belg; 2017 Mar 11; 117(1):359-362. PubMed ID: 27062269
    [No Abstract] [Full Text] [Related]

  • 4. Infantile spasms in a patient with williams syndrome and craniosynostosis.
    Morimoto M, An B, Ogami A, Shin N, Sugino Y, Sawai Y, Usuku T, Tanaka M, Hirai K, Nishimura A, Hasegawa K, Sugimoto T.
    Epilepsia; 2003 Nov 11; 44(11):1459-62. PubMed ID: 14636357
    [Abstract] [Full Text] [Related]

  • 5. Infantile ictal apneas in a child with williams-beuren syndrome.
    Myers KA, McLeod DR, Bello-Espinosa L.
    Pediatr Neurol; 2013 Feb 11; 48(2):149-51. PubMed ID: 23337011
    [Abstract] [Full Text] [Related]

  • 6. [Syndromes 5. Williams-Beuren Syndrome].
    Hoff M, van Hagen JM, Baart JA, Vissink A.
    Ned Tijdschr Tandheelkd; 1998 Oct 11; 105(10):368-9. PubMed ID: 11928452
    [Abstract] [Full Text] [Related]

  • 7. A 22-month-old boy with slow development.
    Charrow J.
    Pediatr Ann; 2005 Apr 11; 34(4):270, 273. PubMed ID: 15871431
    [No Abstract] [Full Text] [Related]

  • 8. Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.
    Mizugishi K, Yamanaka K, Kuwajima K, Kondo I.
    J Hum Genet; 1998 Apr 11; 43(3):178-81. PubMed ID: 9747030
    [Abstract] [Full Text] [Related]

  • 9. Deletion of 7q11.21-q11.23 and infantile spasms without deletion of MAGI2.
    Röthlisberger B, Hoigné I, Huber AR, Brunschwiler W, Capone Mori A.
    Am J Med Genet A; 2010 Feb 11; 152A(2):434-7. PubMed ID: 20101691
    [Abstract] [Full Text] [Related]

  • 10. Sizeable acquired subglottic cyst in a baby with Williams-Beuren syndrome: association or coincidence?
    Christoforidis A, Tsakalides C, Chatziavramidis A, Karagianni P, Dimitriadou M, Konstantinidis I.
    Gene; 2013 Oct 15; 529(1):148-9. PubMed ID: 23954226
    [Abstract] [Full Text] [Related]

  • 11. Partial deletion of the critical 1.5 Mb interval in Williams-Beuren syndrome.
    Heller R, Rauch A, Lüttgen S, Schröder B, Winterpacht A.
    J Med Genet; 2003 Aug 15; 40(8):e99. PubMed ID: 12920091
    [No Abstract] [Full Text] [Related]

  • 12. Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly.
    Komoike Y, Fujii K, Nishimura A, Hiraki Y, Hayashidani M, Shimojima K, Nishizawa T, Higashi K, Yasukawa K, Saitsu H, Miyake N, Mizuguchi T, Matsumoto N, Osawa M, Kohno Y, Higashinakagawa T, Yamamoto T.
    Genesis; 2010 Apr 15; 48(4):233-43. PubMed ID: 20146355
    [Abstract] [Full Text] [Related]

  • 13. Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient.
    Culic V, Culic S, Armanda V, Resic B, Lasan R, Peterlin B.
    Med Pediatr Oncol; 2002 Mar 15; 38(3):205-7. PubMed ID: 11836725
    [No Abstract] [Full Text] [Related]

  • 14. Williams-Beuren Syndrome and Burkitt Leukemia.
    Zhukova N, Naqvi A.
    J Pediatr Hematol Oncol; 2013 Jan 15; 35(1):e30-2. PubMed ID: 23018576
    [Abstract] [Full Text] [Related]

  • 15. Images in cardiovascular medicine. Dynamic left main coronary artery obstruction associated with Williams syndrome.
    Yan BP, Kiernan TJ, Rosenfield K, Garasic JM, de Moor M.
    Circulation; 2009 Jul 14; 120(2):181-2. PubMed ID: 19597063
    [No Abstract] [Full Text] [Related]

  • 16. A new case of keratoconus associated with Williams-Beuren syndrome.
    Viana MM, Frasson M, Leão LL, Stofanko M, Gonçalves-Dornelas H, Cunha Pda S, de Aguiar MJ.
    Ophthalmic Genet; 2013 Sep 14; 34(3):174-7. PubMed ID: 23167938
    [Abstract] [Full Text] [Related]

  • 17. Clinical utility gene card for: Williams-Beuren Syndrome [7q11.23].
    Koehler U, Pabst B, Pober B, Kozel B.
    Eur J Hum Genet; 2014 Sep 14; 22(9):. PubMed ID: 24569604
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
    Zarchi O, Attias J, Raveh E, Basel-Vanagaite L, Saporta L, Gothelf D.
    J Pediatr; 2011 Feb 14; 158(2):301-6. PubMed ID: 20846670
    [Abstract] [Full Text] [Related]

  • 20. [Williams syndrome].
    Kondo I.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():440-3. PubMed ID: 17022583
    [No Abstract] [Full Text] [Related]

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