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Items: 1 to 20 of 71

1.

Sinus of valsalva aneurysm rupture: an unusual presentation of chromosome 22q11.2 deletion: a case report.

Abuchaibe EC, Dobrolet N, Peicher K, Ventura R, Welch E.

Case Rep Pediatr. 2012;2012:387075. doi: 10.1155/2012/387075. Epub 2012 Sep 23.

2.

The four seasons of ruptured sinus of valsalva aneurysms: case presentations and review.

Golzari M, Riebman JB.

Heart Surg Forum. 2004;7(6):E577-83. Review.

PMID:
15769691
3.

Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies.

McElhinney DB, Driscoll DA, Levin ER, Jawad AF, Emanuel BS, Goldmuntz E.

Pediatrics. 2003 Dec;112(6 Pt 1):e472.

PMID:
14654648
4.

Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age.

McElhinney DB, McDonald-McGinn D, Zackai EH, Goldmuntz E.

Pediatrics. 2001 Dec;108(6):E104.

PMID:
11731631
5.

Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.

Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon AP, Keeton BR, Temple IK, Dennis NR.

J Pediatr. 1996 Jul;129(1):26-32.

PMID:
8757559
6.

Ruptured sinus of Valsalva aneurysm with aortic-left atrial fistula.

Davies GJ, Watt J, Muir JR.

Eur J Cardiol. 1975 Oct;3(3):213-8.

PMID:
1183473
7.

[Aneurysm of the sinus of Valsalva in children and young adults. Apropos of 9 cases].

Rey C, Leroy O, Francart C, Marchand X, Ducloux G, Dupuis C.

Arch Mal Coeur Vaiss. 1986 May;79(5):668-75. French.

PMID:
3092766
8.

Anatomic patterns of conotruncal defects associated with deletion 22q11.

Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B.

Genet Med. 2001 Jan-Feb;3(1):45-8.

PMID:
11339377
9.

Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children.

Anilkumar A, Kappanayil M, Thampi MV, Nampoothiri S, Sundaram KR, Vasudevan DM.

Acta Paediatr. 2011 Sep;100(9):e97-100. doi: 10.1111/j.1651-2227.2011.02271.x. Epub 2011 Apr 8.

PMID:
21418101
10.

Chromosomal and cardiovascular anomalies associated with congenital laryngeal web.

McElhinney DB, Jacobs I, McDonald-McGinn DM, Zackai EH, Goldmuntz E.

Int J Pediatr Otorhinolaryngol. 2002 Oct 21;66(1):23-27.

PMID:
12363418
11.

Sinus of Valsalva aneurysm with rupture. Case report and literature review.

Galicia-Tornell MM, Marín-Solís B, Mercado-Astorga O, Espinoza-Anguiano S, Martínez-Martínez M, Villalpando-Mendoza E.

Cir Cir. 2009 Nov-Dec;77(6):441-5. Review. English, Spanish.

PMID:
20433789
12.

Chromosome 22q11 deletion in patients with truncus arteriosus.

McElhinney DB, Driscoll DA, Emanuel BS, Goldmuntz E.

Pediatr Cardiol. 2003 Nov-Dec;24(6):569-73. Epub 2003 Sep 4.

PMID:
12947506
13.

Prenatally diagnosed case of 22q11.2 deletion syndrome associated with pulmonary artery aneurysm.

Ozer L, Lembet A, Uğurlu N, Baltaci V, Balci S.

Turk J Pediatr. 2012 Jan-Feb;54(1):74-6.

PMID:
22397049
14.

Selective IgM deficiency and 22q11.2 deletion syndrome.

Kung SJ, Gripp KW, Stephan MJ, Fairchok MP, McGeady SJ.

Ann Allergy Asthma Immunol. 2007 Jul;99(1):87-92.

PMID:
17650836
15.

Frequency of 22q11 deletions in patients with conotruncal defects.

Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA.

J Am Coll Cardiol. 1998 Aug;32(2):492-8.

16.

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.

McElhinney DB, Clark BJ 3rd, Weinberg PM, Kenton ML, McDonald-McGinn D, Driscoll DA, Zackai EH, Goldmuntz E.

J Am Coll Cardiol. 2001 Jun 15;37(8):2114-9.

17.

[Clinical analysis for 70 sinus of valsalva aneurysm].

Wang ZJ, Fan QX, Zou CW, Li DC, Li HX, Wang AB.

Zhonghua Wai Ke Za Zhi. 2004 Jul 7;42(13):808-11. Chinese.

PMID:
15363302
18.

Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects.

Derbent M, Yilmaz Z, Baltaci V, Saygili A, Varan B, Tokel K.

Am J Med Genet A. 2003 Jan 15;116A(2):129-35.

PMID:
12494430
19.

Outcome of surgery for sinus of Valsalva aneurysm with discrete membranous subaortic stenosis.

Guo HW, Chang Q, Yu CT, Sun XG, Qian XY, Hu SS.

Chin Med J (Engl). 2012 May;125(9):1552-5.

PMID:
22800820
20.

[22q11 deletion syndrome: an expanding phenotype].

Moreno Izco F, Zuazo Zamalloa E, González Alvaredo S, Bereciartu Irastorza P.

Neurologia. 2009 Jan-Feb;24(1):69-71. Spanish.

PMID:
19214819

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