These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

67 related articles for article (PubMed ID: 20958825)

  • 1. Multiple sclerosis in association with Williams-Beuren syndrome.
    Papageorgiou E; Wacker A; Nägele T; Bonin M; Dufke A
    J Paediatr Child Health; 2010 Oct; 46(10):612-4. PubMed ID: 20958825
    [No Abstract]   [Full Text] [Related]  

  • 2. Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome.
    Pankau R; Partsch CJ; Winter M; Gosch A; Wessel A
    Am J Med Genet; 1996 May; 63(1):301-4. PubMed ID: 8723124
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New findings concerning cardiovascular manifestations emerging from long-term follow-up of 150 patients with the Williams-Beuren-Beuren syndrome.
    Del Pasqua A; Rinelli G; Toscano A; Iacobelli R; Digilio C; Marino B; Saffirio C; Mondillo S; Pasquini L; Sanders SP; de Zorzi A
    Cardiol Young; 2009 Dec; 19(6):563-7. PubMed ID: 19941695
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Saccade adaptation in Williams-Beuren Syndrome.
    van der Geest JN; Haselen GC; Frens MA
    Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1464-8. PubMed ID: 16565380
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Morphometric analysis of elastic skin fibres from patients with: cutis laxa, anetoderma, pseudoxanthoma elasticum, and Buschke-Ollendorff and Williams-Beuren syndromes.
    Ghomrasseni S; Dridi M; Bonnefoix M; Septier D; Gogly G; Pellat B; Godeau G
    J Eur Acad Dermatol Venereol; 2001 Jul; 15(4):305-11. PubMed ID: 11730039
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Vascular malformations in the Williams-Beuren syndrome: report of three new cases].
    Sator H; Rhouni FE; Benjouad I; Rhouni FE; Benjouad I; Dafiri R; Chat L
    Pan Afr Med J; 2016; 23():38. PubMed ID: 27200143
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Williams syndrome(Williams-Beuren syndrome), elfin face syndrome].
    Ehara H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):263-5. PubMed ID: 11057222
    [No Abstract]   [Full Text] [Related]  

  • 8. Visual search deficits in Williams-Beuren syndrome.
    Montfoort I; Frens MA; Hooge IT; Haselen GC; van der Geest JN
    Neuropsychologia; 2007 Mar; 45(5):931-8. PubMed ID: 17010393
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Williams-Beuren syndrome.
    Menegazzi JJ
    Science; 2006 Mar; 311(5767):1552. PubMed ID: 16543440
    [No Abstract]   [Full Text] [Related]  

  • 10. The mystery of sudden death in Williams-Beuren syndrome: cardiomyopathy or Kounis syndrome?
    Kounis NG; Soufras GD; Mazarakis A
    Int J Cardiol; 2012 May; 156(3):251-2. PubMed ID: 22078390
    [No Abstract]   [Full Text] [Related]  

  • 11. [Cleft palate and Williams syndrome].
    Vincent C; Mercier JM; David A
    Rev Stomatol Chir Maxillofac; 2008 Feb; 109(1):44-7. PubMed ID: 18164045
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aortic stiffness with the Williams-Beuren syndrome.
    Wessel A; Pankau R; Berdau W; Löns P
    Pediatr Cardiol; 1997; 18(3):244. PubMed ID: 9142724
    [No Abstract]   [Full Text] [Related]  

  • 13. Discovering structure in auditory input: evidence from Williams syndrome.
    Elsabbagh M; Cohen H; Karmiloff-Smith A
    Am J Intellect Dev Disabil; 2010 Mar; 115(2):128-39. PubMed ID: 20441383
    [TBL] [Abstract][Full Text] [Related]  

  • 14. How we approach peripheral pulmonary stenosis in Williams-Beuren syndrome.
    Gandy KL; Tweddell JS; Pelech AN
    Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu; 2009; ():118-21. PubMed ID: 19349025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Williams-Beuren Syndrome with Mirror Movements.
    Işıkay S; Sezer S; Kırık S; Güngör O
    Indian J Pediatr; 2016 Nov; 83(12-13):1493-1494. PubMed ID: 27306224
    [No Abstract]   [Full Text] [Related]  

  • 16. 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; 14(5):507-8. PubMed ID: 16523213
    [No Abstract]   [Full Text] [Related]  

  • 17. Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.
    Ferrero GB; Biamino E; Sorasio L; Banaudi E; Peruzzi L; Forzano S; di Cantogno LV; Silengo MC
    Eur J Med Genet; 2007; 50(5):327-37. PubMed ID: 17625998
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 145C(3):280-90. PubMed ID: 17639596
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Williams-Beuren syndrome associated with caudal regression syndrome and coagulopathy--a case report.
    Singer G; Schalamon J; Ainoedhofer H; Petek E; Kroisel PM; Höllwarth ME
    J Pediatr Surg; 2005 Nov; 40(11):e47-50. PubMed ID: 16291141
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.