115 related articles for article (PubMed ID: 9558923)
21. [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]
22. [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]
23. [William-Beuren syndrome: description of a case].
Bonvini G; Cotta-Ramusino A; Ricciardi G; Pagliano-Sassi L
Pediatr Med Chir; 1991; 13(5):519-22. PubMed ID: 1788114
[TBL] [Abstract][Full Text] [Related]
24. Concurrence of supravalvular aortic stenosis and peripheral pulmonary stenosis in three generations of a family: a form of arterial dysplasia.
Kumar A; Stalker HJ; Williams CA
Am J Med Genet; 1993 Mar; 45(6):739-42. PubMed ID: 8456853
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. Parieto-occipital grey matter abnormalities in children with Williams syndrome.
Boddaert N; Mochel F; Meresse I; Seidenwurm D; Cachia A; Brunelle F; Lyonnet S; Zilbovicius M
Neuroimage; 2006 Apr; 30(3):721-5. PubMed ID: 16380272
[TBL] [Abstract][Full Text] [Related]
28. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
Piver MS
Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
[TBL] [Abstract][Full Text] [Related]
29. A Case of William's Syndrome in a Ugandan Child: A Feasible Diagnosis Even in a Low-Resource Setting.
Mapelli M; Zagni P; Calbi V; Twalib A; Ferrara R; Agostoni P
Children (Basel); 2021 Dec; 8(12):. PubMed ID: 34943388
[TBL] [Abstract][Full Text] [Related]
30. Familial occurrence of idiopathic infantile hypercalcemia.
McTaggart SJ; Craig J; MacMillan J; Burke JR
Pediatr Nephrol; 1999 Oct; 13(8):668-71. PubMed ID: 10502124
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams-Beuren syndrome regions.
Kirchhoff M; Bisgaard AM; Bryndorf T; Gerdes T
Eur J Med Genet; 2007; 50(1):33-42. PubMed ID: 17090394
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. [Williams syndrome: clinical, cytogenetical, neurophysiological and neuroanatomic study].
Aravena T; Castillo S; Carrasco X; Mena I; López J; Rojas JP; Rosemberg C; Schröter C; Aboitiz F
Rev Med Chil; 2002 Jun; 130(6):631-7. PubMed ID: 12194685
[TBL] [Abstract][Full Text] [Related]
35. [Magnetic resonance features of supravalvular aortic stenosis in William's syndrome. Report of 2 cases].
Di Cesare E; Sabatini M; Splendiani A; Masciocchi C
Radiol Med; 1998; 96(1-2):113-5. PubMed ID: 9819633
[No Abstract] [Full Text] [Related]
36. Williams Syndrome With Rare Ureteric Abnormality.
Khan J; Al-Obaidy KI; Fan R
Cureus; 2021 Aug; 13(8):e17210. PubMed ID: 34540437
[TBL] [Abstract][Full Text] [Related]
37. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
Stoll C; Terzic J; Fischbach M
Genet Couns; 1999; 10(4):337-43. PubMed ID: 10631920
[TBL] [Abstract][Full Text] [Related]
38. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Van der Aa N; Rooms L; Vandeweyer G; van den Ende J; Reyniers E; Fichera M; Romano C; Delle Chiaie B; Mortier G; Menten B; Destrée A; Maystadt I; Männik K; Kurg A; Reimand T; McMullan D; Oley C; Brueton L; Bongers EM; van Bon BW; Pfund R; Jacquemont S; Ferrarini A; Martinet D; Schrander-Stumpel C; Stegmann AP; Frints SG; de Vries BB; Ceulemans B; Kooy RF
Eur J Med Genet; 2009; 52(2-3):94-100. PubMed ID: 19249392
[TBL] [Abstract][Full Text] [Related]
39. [Williams' and Beuren's syndrome with hypertension and associated renal abnormalities].
Fischbach M; Lutz JD; Tongio J; Sauvage P; Geisert J; Levy JM
Ann Pediatr (Paris); 1978 Dec; 25(10):596-600. PubMed ID: 16114149
[No Abstract] [Full Text] [Related]
40. [History of Williams syndrome].
Bzdúch V; Jariabková K
Cas Lek Cesk; 2002 Oct; 141(20):651-5. PubMed ID: 12515042
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]