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Items: 6

1.

Pulmonary artery-focused contrast echocardiography with supplemental oxygen(PCESO) for echocardiographic diagnosis of anomalous origin of left coronary artery from pulmonary artery: Novel use of an old technique.

Malakan Rad E, Aghaei-Moghadam E, Mirzaaghayan MR, Pouraliakbar HR.

Clin Case Rep. 2019 Aug 13;7(9):1777-1781. doi: 10.1002/ccr3.2354. eCollection 2019 Sep.

2.

Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.

Mohammadzadeh A, Akbaroghli S, Aghaei-Moghadam E, Mahdieh N, Badv RS, Jamali P, Kariminejad R, Chavoshzadeh Z, Ghasemi Firouzabadi S, Mansour Ghanaie R, Nozari A, Banihashemi S, Hadipour F, Hadipour Z, Kariminejad A, Najmabadi H, Shafeghati Y, Behjati F.

Cell J. 2019 Oct;21(3):337-349. doi: 10.22074/ cellj.2019.6053. Epub 2019 Jun 15.

3.

Truncus arteriosus associated with double aortic arch in a patient with DiGeorge syndrome: A rare case report.

Moghadam EA, Mirzaaghayan MR, Zeinaloo A, Mohebbi A, Ghamari A.

Ann Pediatr Cardiol. 2019 May-Aug;12(2):185-186. doi: 10.4103/apc.APC_80_18. No abstract available.

4.

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family.

Nozari A, Aghaei-Moghadam E, Zeinaloo A, Alavi A, Ghasemi Firouzabdi S, Minaee S, Eskandari Hesari M, Behjati F.

Cell J. 2019 Apr;21(1):70-77. doi: 10.22074/cellj.2019.5734. Epub 2018 Nov 18.

5.

A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family.

Nozari A, Aghaei-Moghadam E, Zeinaloo A, Mollazadeh R, Majnoon MT, Alavi A, Ghasemi Firouzabadi S, Mohammadzadeh A, Banihashemi S, Nikzaban M, Najmabadi H, Behjati F.

Gene. 2018 Jun 15;659:160-167. doi: 10.1016/j.gene.2018.03.044. Epub 2018 Mar 15.

PMID:
29551499
6.

Patent ductus arteriousus device closure in an infant with rubinstein-taybi syndrome.

Aghaei-Moghadam E, Zanjani KS, Ghandi Y.

Iran J Pediatr. 2013 Dec;23(6):708-9. No abstract available.

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