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Items: 17

1.

Autosomal dominant inheritance of left ventricular outflow tract obstruction.

Wessels MW, Berger RM, Frohn-Mulder IM, Roos-Hesselink JW, Hoogeboom JJ, Mancini GS, Bartelings MM, Krijger Rd, Wladimiroff JW, Niermeijer MF, Grossfeld P, Willems PJ.

Am J Med Genet A. 2005 Apr 15;134A(2):171-9.

PMID:
15712195
2.

Management options in neonates and infants with critical left ventricular outflow tract obstruction.

Alsoufi B, Karamlou T, McCrindle BW, Caldarone CA.

Eur J Cardiothorac Surg. 2007 Jun;31(6):1013-21. Epub 2007 Apr 9. Review. Erratum in: Eur J Cardiothorac Surg. 2007 Sep;32(3):558.

PMID:
17416536
3.

Molecular determinants of left and right outflow tract obstruction.

Towbin JA, Belmont J.

Am J Med Genet. 2000 Winter;97(4):297-303. Review.

PMID:
11376441
4.

Left outflow tract anomalies in children.

Loscalzo ML.

Curr Opin Pediatr. 2010 Oct;22(5):593-7. doi: 10.1097/MOP.0b013e32833e130f. Review.

PMID:
20736838
5.

Adams-Oliver syndrome associated with cardiovascular malformations.

Lin AE, Westgate MN, van der Velde ME, Lacro RV, Holmes LB.

Clin Dysmorphol. 1998 Oct;7(4):235-41. Review.

PMID:
9823488
6.
7.

Genetics of left ventricular outflow tract abnormalities.

De Backer J.

Acta Cardiol. 2006 Apr;61(2):202-3. Review. No abstract available.

PMID:
16716025
8.
9.

A family with autosomal dominant oculo-auriculo-vertebral spectrum.

Tasse C, Majewski F, Böhringer S, Fischer S, Lüdecke HJ, Gillessen-Kaesbach G, Wieczorek D.

Clin Dysmorphol. 2007 Jan;16(1):1-7. Review.

PMID:
17159507
11.

Accessory mitral valve tissue: a case report and an updated review of literature.

Yuan SM, Shinfeld A, Mishaly D, Haizler R, Ghosh P, Raanani E.

J Card Surg. 2008 Nov-Dec;23(6):769-72. doi: 10.1111/j.1540-8191.2008.00633.x. Review.

PMID:
19017009
12.
13.

Congenital left heart outflow abnormalities in the newborn.

Suys B, De Groote K, Decaluwe W, Panzer J, Francois K, Bové T, Matthys D, Verhaaren H, De Wolf D.

Acta Cardiol. 2006 Apr;61(2):210-1. Review. No abstract available.

PMID:
16716030
14.

A rare case of aortic coarctation and ventricular septal defect combined with alveolar capillary dysplasia.

Taborosi B, Tödt-Pingel I, Kayser G, Dittrich S.

Pediatr Cardiol. 2007 Jul-Aug;28(4):319-23. Epub 2007 May 25. Review.

PMID:
17530317
15.

Oculoauriculovertebral spectrum: report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature.

Vendramini-Pittoli S, Kokitsu-Nakata NM.

Clin Dysmorphol. 2009 Apr;18(2):67-77. doi: 10.1097/MCD.0b013e328323a7dd. Review.

PMID:
19305190
16.

[Easy echo diagnosis for hypotension and shock].

Otsuji Y.

J UOEH. 2008 Dec 1;30(4):431-42. Review. Japanese.

PMID:
19086701
17.

The molecular basis of vascular disorders.

Towbin JA, Casey B, Belmont J.

Am J Hum Genet. 1999 Mar;64(3):678-84. Review. No abstract available.

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