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Clinical Nutrition ESPEN|July 31, 2021
Food intake and attention-deficit/hyperactivity disorder in children: A case_control studyAtena Jamshidnia, Mehdi Tavallaei, Mahdieh Hosseinzadeh
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|November 3, 2021
Postoperative outcomes of intrasphincteric botox injection during hemorrhoidectomy: A double-blind clinical trialMina Alvandipour, Mehdi Tavallaei, Fatemeh Rezaei, et al.
Clinical Medicine Insights. Case Reports|July 15, 2021
Intentional Ingestion of a Metallic Wire Causing Perforation and Retroperitoneal Abscess: A Case ReportMehdi Tavallaei, Mahsa Bahadorinia, Arsh Haj Mohamad Ebrahim Ketabforoush
Clinical Medicine Insights. Case Reports|April 25, 2022
Multiple Complex Complications After Redo Bariatric Surgery (Infrequent Complication: Fistula Between the Splenic Artery and the Remnant of the Stomach): A Case ReportMohammadreza Abdolhosseini, Arsh Haj Mohamad Ebrahim Ketabforoush, Parynaz Parhizgar, et al.
International Journal of Surgery Case Reports|January 5, 2021
Paratubal endosalpingiosis: a case reportFatemeh Sadat Mahdavi, Mehdi Tavallaei, Arsh Haj Mohamad Ebrahim Ketabforoush, et al.
European Journal of Translational Myology|May 19, 2022
May position of hemodialysis catheter tip have a direct effect on its patency? Positive results of a preliminary study on its rotationMohammad Hassani, Mahdi Mohebbi, Mehdi Tavallaei, et al.
Techniques in Coloproctology|November 13, 2022
Fistulectomy and primary sphincteroplasty in complex anal fistula treatment: a hospital-based long-term follow-up studyFakhrosadat Anaraki, Mohammad Reza Nikshoar, Arsh Haj Mohamad Ebrahim Ketabforoush, et al.
Gastroenterology and Hepatology From Bed to Bench|September 28, 2023
A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case studyBinazir Khanabadi, Diba Najafgholizadeh Seyfi, Leili Rejali, et al.
Cancer Reports (Hoboken, N.J.)|November 3, 2023
Rare single-nucleotide variants of MLH1 and MSH2 genes in patients with Lynch syndromeSeyed Mohsen Mirabdolhosseini, Mohammad Yaghoob Taleghani, Leili Rejali, et al.
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