Literature DB >> 7677092

Tetralogy of Fallot associated with chromosome 22q11 deletion.

K Momma1, C Kondo, M Ando, R Matsuoka, A Takao.   

Abstract

Mesh：

Year:  1995        PMID： 7677092     DOI： 10.1016/s0002-9149(99)80170-2

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN： 0002-9149            Impact factor:   2.778


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  17 in total

Review 1.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

2.  Ductal stent implantation in tetralogy of fallot with aortic arch abnormality.

Authors:  Hasan Tahsin Tola; Yakup Ergul; Murat Saygi; Isa Ozyilmaz; Alper Guzeltas; Ender Odemis
Journal:  Tex Heart Inst J       Date:  2015-06-01

3.  The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease.

Authors:  K Devriendt; B Eyskens; A Swillen; M Dumoulin; M Gewillig; J P Fryns
Journal:  Eur J Pediatr       Date:  1996-08       Impact factor: 3.183

4.  Congenital isolation of the subclavian artery in adults.

Authors:  J L Reynolds
Journal:  Tex Heart Inst J       Date:  1997

5.  Surgical correction of isolated unilateral absence of right pulmonary artery.

Authors:  Takeshi Hiramatsu; Shigeru Komori; Yoshitaka Okamura; Hiroyuki Suzuki; Takashi Takeuchi; Syoichi Shibuta
Journal:  Heart Vessels       Date:  2010-07-31       Impact factor: 2.037

6.  NRP1 haploinsufficiency predisposes to the development of Tetralogy of Fallot.

Authors:  Ivan Duran; Jessica Tenney; Carmen M Warren; Anna Sarukhanov; Fabiana Csukasi; Mark Skalansky; Maria L Iruela-Arispe; Deborah Krakow
Journal:  Am J Med Genet A       Date:  2018-01-24       Impact factor: 2.802

7.  Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: outflow tract obstruction, coarctation of the aorta, tetralogy of Fallot, Ebstein anomaly and Marfan's syndrome.

Authors:  Candice K Silversides; Marla Kiess; Luc Beauchesne; Timothy Bradley; Michael Connelly; Koichiro Niwa; Barbara Mulder; Gary Webb; Jack Colman; Judith Therrien
Journal:  Can J Cardiol       Date:  2010-03       Impact factor: 5.223

Review 8.  Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Authors:  Marta Unolt; Paolo Versacci; Silvia Anaclerio; Caterina Lambiase; Giulio Calcagni; Matteo Trezzi; Adriano Carotti; Terrence Blaine Crowley; Elaine H Zackai; Elizabeth Goldmuntz; James William Gaynor; Maria Cristina Digilio; Donna M McDonald-McGinn; Bruno Marino
Journal:  Am J Med Genet A       Date:  2018-04-16       Impact factor: 2.802

9.  Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.

Authors:  Lidia Ziolkowska; Wanda Kawalec; Anna Turska-Kmiec; Malgorzata Krajewska-Walasek; Grazyna Brzezinska-Rajszys; Jadwiga Daszkowska; Bogdan Maruszewski; Piotr Burczynski
Journal:  Eur J Pediatr       Date:  2008-01-03       Impact factor: 3.183

10.  Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.

Authors:  Wai Lun Alan Fung; Eva W C Chow; Gary D Webb; Michael A Gatzoulis; Anne S Bassett
Journal:  Int J Cardiol       Date:  2008-01-11       Impact factor: 4.164
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