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Results: 1 to 20 of 97

1.

Williams-Beuren syndrome: historical aspects.

Berdon WE, Clarkson PM, Teele RL.

Pediatr Radiol. 2011 Feb;41(2):262-6. doi: 10.1007/s00247-010-1908-z. Epub 2010 Dec 1.

PMID:
21120465
[PubMed - indexed for MEDLINE]
2.

John C. P. Williams of Williams-Beuren syndrome.

Lenhoff HM, Teele RL, Clarkson PM, Berdon WE.

Pediatr Radiol. 2011 Feb;41(2):267-9. doi: 10.1007/s00247-010-1909-y. Epub 2010 Nov 25.

PMID:
21107555
[PubMed - indexed for MEDLINE]
3.

The genomic basis of the Williams-Beuren syndrome.

Schubert C.

Cell Mol Life Sci. 2009 Apr;66(7):1178-97. doi: 10.1007/s00018-008-8401-y. Review.

PMID:
19039520
[PubMed - indexed for MEDLINE]
4.

[The mistery of J.C.P. Williams].

Kotsias BA.

Medicina (B Aires). 2013;73(1):81-2. Spanish. No abstract available.

PMID:
23335713
[PubMed - indexed for MEDLINE]
Free Article
5.

Williams syndrome: 15 years of psychological research.

Mervis CB.

Dev Neuropsychol. 2003;23(1-2):1-12. Review.

PMID:
12730017
[PubMed - indexed for MEDLINE]
6.

Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.

Yau EK, Lo IF, Lam ST.

Hong Kong Med J. 2004 Feb;10(1):22-7.

PMID:
14967851
[PubMed - indexed for MEDLINE]
Free Article
7.

Williams-Beuren syndrome diagnosis using fluorescence in situ hybridization.

Osborne LR, Joseph-George AM, Scherer SW.

Methods Mol Med. 2006;126:113-28.

PMID:
16930009
[PubMed - indexed for MEDLINE]
8.

[Clinical aspects and genetics of Williams-Beuren syndrome. Clinical and molecular genetic study of 44 patients with suspected Williams-Beuren syndrome].

von Beust G, Laccone FA, del Pilar Andrino M, Wessel A.

Klin Padiatr. 2000 Nov-Dec;212(6):299-307. German.

PMID:
11190824
[PubMed - indexed for MEDLINE]
9.

Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH).

Sugayama SM, Koch VH, Furusawa EA, Leone C, Kim CA.

Rev Hosp Clin Fac Med Sao Paulo. 2004 Oct;59(5):266-72. Epub 2004 Oct 29.

PMID:
15543398
[PubMed - indexed for MEDLINE]
Free Article
10.

[History of Williams syndrome].

Bzdúch V, Jariabková K.

Cas Lek Cesk. 2002 Oct 11;141(20):651-5. Slovak.

PMID:
12515042
[PubMed - indexed for MEDLINE]
11.

Williams-Beuren syndrome: genes and mechanisms.

Francke U.

Hum Mol Genet. 1999;8(10):1947-54. Review.

PMID:
10469848
[PubMed - indexed for MEDLINE]
Free Article
12.

Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.

Osborne LR, Campbell T, Daradich A, Scherer SW, Tsui LC.

Genomics. 1999 Apr 15;57(2):279-84.

PMID:
10198167
[PubMed - indexed for MEDLINE]
13.

Transcriptome profile in Williams-Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficits.

Antonell A, Vilardell M, Pérez Jurado LA.

Hum Genet. 2010 Jul;128(1):27-37. doi: 10.1007/s00439-010-0817-4. Epub 2010 Apr 17.

PMID:
20401492
[PubMed - indexed for MEDLINE]
14.

[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. doi: 10.1016/j.arcped.2008.11.011. Epub 2008 Dec 18. Review. French.

PMID:
19097873
[PubMed - indexed for MEDLINE]
15.

Familial Williams-Beuren syndrome showing varying clinical expression.

Pankau R, Siebert R, Kautza M, Schneppenheim R, Gosch A, Wessel A, Partsch CJ.

Am J Med Genet. 2001 Feb 1;98(4):324-9. Review.

PMID:
11170076
[PubMed - indexed for MEDLINE]
16.

[The supremacy of vision in medical diagnostics : Prof. Stefan Feuerbach's 65th birthday].

Dietl B.

Radiologe. 2011 Jan;51(1):56-8. doi: 10.1007/s00117-010-2111-9. German. No abstract available.

PMID:
21174072
[PubMed - indexed for MEDLINE]
17.

Arterial hypertension in a child with Williams-Beuren syndrome (7q11.23 chromosomal deletion).

Sylos Cd, Pereira AC, Azeka E, Miura N, Mesquita SM, Ebaid M.

Arq Bras Cardiol. 2002 Aug;79(2):173-80. English, Portuguese.

PMID:
12219191
[PubMed - indexed for MEDLINE]
Free Article
18.

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.

PMID:
11730039
[PubMed - indexed for MEDLINE]
19.

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. No abstract available.

PMID:
16523213
[PubMed - indexed for MEDLINE]
Free Article
20.

[25 years of progress in neurology: an indispensable part of emergency medical care today].

Straube A.

MMW Fortschr Med. 2008 Nov 27;150(48):154, 156, 158. German. No abstract available.

PMID:
19125527
[PubMed - indexed for MEDLINE]

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