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https://www.readbyqxmd.com/read/24908348/maximized-left-atrial-dome-approach-for-left-atrial-tumor-resection
#1
Syed T Hussain, Mazin Alsalihi, Eugene H Blackstone, Gösta B Pettersson
No abstract text is available yet for this article.
August 2014: Journal of Thoracic and Cardiovascular Surgery
https://www.readbyqxmd.com/read/24876984/troubling-toys-rare-earth-magnet-ingestion-in-children-causing-bowel-perforations
#2
Parkash Mandhan, Muthana Alsalihi, Saleem Mammoo, Mansour J Ali
Ingestion of foreign bodies in the pediatric population is common and magnet ingestion is known to cause a significant morbidity. Rare-earth magnets are small 3-6 mm diameter spherical powerful magnets that are sold as popular desk toys for adults and were previously found in construction toys in attractive colors for children to play with. We describe 2 young healthy children who ingested rare-earth magnets Buckyballs while playing with these magnetic toys and later presented in emergency with acute abdomen...
2014: Case Reports in Pediatrics
https://www.readbyqxmd.com/read/23286971/midterm-results-of-david-reimplantation-in-patients-with-connective-tissue-disorder
#3
Lars G Svensson, Eugene H Blackstone, Mazin Alsalihi, Lillian H Batizy, Eric E Roselli, Rebecca McCullough, Alessandro Vivacqua, Rocio T Moran, A Marc Gillinov, Maran Thamilarasan, Brian Griffin, Donald F Hammer, William J Stewart, Joseph F Sabik, Bruce W Lytle
BACKGROUND: Few series have examined follow-up risks of the David reimplantation operation in patients with connective tissue disorder. Hence, we assessed its midterm safety and effectiveness for Marfan syndrome and other connective tissue disorders, such as Ehlers-Danlos, Loeys-Dietz, and marfanoid syndromes. METHODS: Of 313 patients who underwent modified David reimplantation, 178 identified as having connective tissue disorders underwent operation from January 1, 1991, to December 31, 2010...
February 2013: Annals of Thoracic Surgery
https://www.readbyqxmd.com/read/22901940/female-double-urethra-a-case-report
#4
Adel Ismail, Talal Al Rayes, Muthana Alsalihi, Tariq Abbas
Female double urethra is a very rare anomaly, with less than 40 cases reported since 1970. Most reported cases of double urethra are in the sagittal plane and tend to be stenotic. We describe a 4-year-old girl with double urethra, which was not stenotic and was in the coronal plane. Double urethra should be excluded among other causes in any girl who is incontinent beyond the continence age.
August 2012: Journal of Pediatric Surgery
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