Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Malek M. El Yaman"'
Publikováno v:
Pediatrics and Neonatology, Vol 57, Iss 3, Pp 236-239 (2016)
Scimitar syndrome is a rare congenital anomaly characterized by partial anomalous pulmonary venous drainage of the right lung to the inferior vena cava (IVC) creating a tubular opacity paralleling the right cardiac border on chest radiography which r
Autor:
Harold M. Burkhart, Nandan S. Anavekar, Paul R. Julsrud, Andrew J. Miller, John A. Miller, Malek M. El Yaman
Publikováno v:
The International Journal of Cardiovascular Imaging. 28:1525-1532
Certain coronary anomalies are associated with high risk features. We sought to determine the diagnostic accuracy of coronary computed tomographic angiography (CTA) in determining high-risk features, particularly intramural segments. Anomalous corona
Publikováno v:
Congenital Heart Disease. 2:446-450
Aorto-left atrial fistula is a rare entity in which the integrity of the aortic root bordering the left atrium is disrupted. The clinical presentation is highly variable, depending predominantly on the size of the fistula and the pressure difference
Publikováno v:
Pediatric cardiology. 36(5)
MRI is a valuable noninvasive tool that helps in predicting the type of cardiac tumors and guiding management decisions. Several reports have described the appearance of cardiac fibromas on MRI, which typically show hyperenhancement on myocardial del
Publikováno v:
Heart Rhythm. 5:472-474
l@ ntroduction ongenital long QT syndrome (LQTS) is a heterogene roup of primary and secondary cardiac channelopath haracterized by delayed myocardial repolarization, Q rolongation, and increased risk of sudden death. Ele QTS-susceptibility genes hav
Autor:
Malek M El Yaman, David J Tester, Argelia Medeiros Domingo, Carla M Haglund, Michael J Ackerman
Publikováno v:
Circulation. 118
Long QT syndrome (LQTS) is a heterogeneous group of channelopathies characterized by increased risk of potentially lethal ventricular arrhythmias. LQT1, LQT2, and LQT3 comprise 95% of genetically proven cases and exhibit a number of established genot
Publikováno v:
Circulation. 116
Background: Although multiple macroreentrant atrial flutters are seen in postoperative patients with congenital heart disease, cavotricuspid isthmus (CVTI) dependent flutter remains a fairly common arrhythmia in this group. When a Fontan or atrial sw
Autor:
Lastinger A; Department of Pediatrics-Internal Medicine, WVU School of Medicine, Morgantown, WV 26505, USA., El Yaman M; Department of Pediatrics, WVU School of Medicine, Morgantown, WV 26505, USA., Gustafson R; Department of Pediatric Cardiovascular and Thoracic Surgery, WVU School of Medicine, Morgantown, WV 26505, USA., Yossuck P; Department of Pediatrics-Internal Medicine, WVU School of Medicine, Morgantown, WV 26505, USA. Electronic address: pyossuck@hsc.wvu.edu.
Publikováno v:
Pediatrics and neonatology [Pediatr Neonatol] 2016 Jun; Vol. 57 (3), pp. 236-9. Date of Electronic Publication: 2013 Oct 23.
Autor:
El Yaman M; Department of Pediatrics/Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN 55905, USA., Perry J, Makielski JC, Ackerman MJ
Publikováno v:
Heart rhythm [Heart Rhythm] 2008 Mar; Vol. 5 (3), pp. 472-4. Date of Electronic Publication: 2007 Oct 18.