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Items: 1 to 20 of 102

1.

Intracranial arteries in individuals with the elastin gene hemideletion of Williams syndrome.

Wint DP, Butman JA, Masdeu JC, Meyer-Lindenberg A, Mervis CB, Sarpal D, Morris CA, Berman KF.

AJNR Am J Neuroradiol. 2014 Jan;35(1):90-4. doi: 10.3174/ajnr.A3641. Epub 2013 Jul 18.

2.

Disruption of the elastin gene in adult Williams syndrome is accompanied by a paradoxical reduction in arterial stiffness.

Lacolley P, Boutouyrie P, Glukhova M, Daniel Lamaziere JM, Plouin PF, Bruneval P, Vuong P, Corvol P, Laurent S.

Clin Sci (Lond). 2002 Jul;103(1):21-9.

PMID:
12095400
3.

Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndrome.

Urbán Z, Riazi S, Seidl TL, Katahira J, Smoot LB, Chitayat D, Boyd CD, Hinek A.

Am J Hum Genet. 2002 Jul;71(1):30-44. Epub 2002 May 6.

4.

Ischemic stroke and intracranial multifocal cerebral arteriopathy in Williams syndrome.

Soper R, Chaloupka JC, Fayad PB, Greally JM, Shaywitz BA, Awad IA, Pober BR.

J Pediatr. 1995 Jun;126(6):945-8.

PMID:
7776102
5.

Non-stenotic intracranial arteries have atherosclerotic changes in acute ischemic stroke patients: a 3T MRI study.

Lee WJ, Choi HS, Jang J, Sung J, Kim TW, Koo J, Shin YS, Jung SL, Ahn KJ, Kim BS.

Neuroradiology. 2015 Oct;57(10):1007-13. doi: 10.1007/s00234-015-1566-9. Epub 2015 Jul 22.

PMID:
26198422
6.

FISH analysis in patients with clinical diagnosis of Williams syndrome.

Elçioglu N, Mackie-Ogilvie C, Daker M, Berry AC.

Acta Paediatr. 1998 Jan;87(1):48-53. Review.

PMID:
9510447
7.

Elastin gene deletions in Williams syndrome.

Smoot LB.

Curr Opin Pediatr. 1995 Dec;7(6):698-701. Review.

PMID:
8776022
8.

Spontaneous cervical artery dissection in adult Williams syndrome.

Vanacker P, Thijs V.

Cerebrovasc Dis. 2009;27(3):309-10. doi: 10.1159/000201559. Epub 2009 Feb 11. No abstract available.

9.

Intracranial arterial dolichoectasia in autosomal dominant polycystic kidney disease.

Schievink WI, Torres VE, Wiebers DO, Huston J 3rd.

J Am Soc Nephrol. 1997 Aug;8(8):1298-303.

10.

[Dolichoectatic intracranial arteries. Advances in images and therapeutics].

Casas Parera I, Abruzzi M, Lehkuniec E, Schuster G, Muchnik S.

Medicina (B Aires). 1995;55(1):59-68. Review. Spanish.

PMID:
7565039
11.

[Genetic diagnosis of Williams syndrome].

Urbán Z, Kiss E, Kádár K, Szabolcs J, Csiszár K, Boyd DC, Fekete G.

Orv Hetil. 1997 Jul 6;138(27):1749-52. Review. Hungarian.

PMID:
9273487
13.

Arterial spin labeling perfusion MRI in children and young adults with previous ischemic stroke and unilateral intracranial arteriopathy.

Bulder MM, Bokkers RP, Hendrikse J, Kappelle LJ, Braun KP, Klijn CJ.

Cerebrovasc Dis. 2014;37(1):14-21. doi: 10.1159/000355889. Epub 2013 Dec 17.

PMID:
24355934
14.

Anomalies of the abdominal aorta in Williams-Beuren syndrome--another cause of arterial hypertension.

Rose C, Wessel A, Pankau R, Partsch CJ, Bürsch J.

Eur J Pediatr. 2001 Nov;160(11):655-8.

PMID:
11760021
15.

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.

Doyle TF, Bellugi U, Korenberg JR, Graham J.

Am J Med Genet A. 2004 Jan 30;124A(3):263-73.

PMID:
14708099
16.

[Diagnosis of intracranial occlusive vascular disease and evaluation of extracranial-intracranial (EC/IC) arterial bypass using three-dimensional magnetic resonance angiography].

Aoki T, Houkin K, Kamiyama H, Iwasaki Y, Abe H, Koiwa M, Kawaguchi S, Kashiwaba T.

No To Shinkei. 1993 Jan;45(1):57-62. Japanese.

PMID:
8476655
17.

Williams syndrome and related disorders.

Morris CA, Mervis CB.

Annu Rev Genomics Hum Genet. 2000;1:461-84. Review.

PMID:
11701637
18.

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;34(3):174-7. doi: 10.3109/13816810.2012.739257. Epub 2012 Nov 20.

PMID:
23167938
19.
20.

Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.

Brewer CM, Morrison N, Tolmie JL.

Arch Dis Child. 1996 Jan;74(1):59-61.

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