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.
219 related articles for article (PubMed ID: 19764675)
1. Occurrence of anaplastic oligodendroglioma in a patient with Williams syndrome: a case report with analysis of mutational profile of tumor. Omalu BI; Nnebe-Agumadu UH Niger J Clin Pract; 2009 Jun; 12(2):200-4. PubMed ID: 19764675 [TBL] [Abstract][Full Text] [Related]
2. 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; 43(3):178-81. PubMed ID: 9747030 [TBL] [Abstract][Full Text] [Related]
3. [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; 113(2):46-9. PubMed ID: 10425618 [TBL] [Abstract][Full Text] [Related]
4. [Genetic diagnosis of Williams syndrome]. Urbán Z; Kiss E; Kádár K; Szabolcs J; Csiszár K; Boyd DC; Fekete G Orv Hetil; 1997 Jul; 138(27):1749-52. PubMed ID: 9273487 [TBL] [Abstract][Full Text] [Related]
5. [Williams syndrome without cardiovascular abnormalities]. Cincinnati P; Genuardi M; Rutiloni C Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296 [TBL] [Abstract][Full Text] [Related]
6. Combined 1p/19q loss in oligodendroglial tumors: predictive or prognostic biomarker? Weller M; Berger H; Hartmann C; Schramm J; Westphal M; Simon M; Goldbrunner R; Krex D; Steinbach JP; Ostertag CB; Loeffler M; Pietsch T; von Deimling A; Clin Cancer Res; 2007 Dec; 13(23):6933-7. PubMed ID: 18056167 [TBL] [Abstract][Full Text] [Related]
8. [Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects]. van Hagen JM; Govaerts LC; de Coo IF; Gille JJ; Nieuwint AW; Madan K Ned Tijdschr Geneeskd; 2001 Mar; 145(9):396-400. PubMed ID: 11253493 [TBL] [Abstract][Full Text] [Related]
9. [Williams-Beuren syndrome: a multidisciplinary approach]. Lacroix A; Pezet M; Capel A; Bonnet D; Hennequin M; Jacob MP; Bricca G; Couet D; Faury G; Bernicot J; Gilbert-Dussardier B Arch Pediatr; 2009 Mar; 16(3):273-82. PubMed ID: 19097873 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Non-Hodgkin lymphoma in a child with Williams syndrome. Amenta S; Moschovi M; Sofocleous C; Kostaridou S; Mavrou A; Fryssira H Cancer Genet Cytogenet; 2004 Oct; 154(1):86-8. PubMed ID: 15381380 [TBL] [Abstract][Full Text] [Related]
12. Disseminating anaplastic brainstem oligodendroglioma associated with allelic loss in the tumor suppressor candidate region D19S246 of chromosome 19 mimicking an inflammatory central nervous system disease in a 9-year-old boy. Mittelbronn M; Wolff M; Bültmann E; Nägele T; Capper D; Beck R; Meyermann R; Beschorner R Hum Pathol; 2005 Jul; 36(7):854-7. PubMed ID: 16084959 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Is the 1p/19q deletion a diagnostic marker of oligodendrogliomas? Gadji M; Fortin D; Tsanaclis AM; Drouin R Cancer Genet Cytogenet; 2009 Oct; 194(1):12-22. PubMed ID: 19737649 [TBL] [Abstract][Full Text] [Related]
15. Panel review of anaplastic oligodendroglioma from European Organization For Research and Treatment of Cancer Trial 26951: assessment of consensus in diagnosis, influence of 1p/19q loss, and correlations with outcome. Kros JM; Gorlia T; Kouwenhoven MC; Zheng PP; Collins VP; Figarella-Branger D; Giangaspero F; Giannini C; Mokhtari K; Mørk SJ; Paetau A; Reifenberger G; van den Bent MJ J Neuropathol Exp Neurol; 2007 Jun; 66(6):545-51. PubMed ID: 17549014 [TBL] [Abstract][Full Text] [Related]
16. Novel genomic alterations and mechanisms associated with tumor progression in oligodendroglioma and mixed oligoastrocytoma. Blesa D; Mollejo M; Ruano Y; de Lope AR; Fiaño C; Ribalta T; García JF; Campos-Martín Y; Hernández-Moneo JL; Cigudosa JC; Meléndez B J Neuropathol Exp Neurol; 2009 Mar; 68(3):274-85. PubMed ID: 19225409 [TBL] [Abstract][Full Text] [Related]
17. 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 [TBL] [Abstract][Full Text] [Related]
18. Autism and Williams syndrome: a case report. Herguner S; Mukaddes NM World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145 [TBL] [Abstract][Full Text] [Related]