Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ophir Gilad"'
Autor:
Sharif Yassin, Noa Sori, Ophir Gilad, Mati Shnell, Relly Richer, Nir Bar, Yishai Ron, Nathaniel Aviv Cohen, Subhi Abu-Abeid, Danit Dayan, Shai Meron Eldar, Shira Zelber-Sagi, Sigal Fishman
Publikováno v:
International Journal of Gastrointestinal Intervention, Vol 13, Iss 1, Pp 16-22 (2024)
Background: Functional bowel disorders (FBDs), including irritable bowel syndrome (IBS), are common worldwide. Recently, increasingly many bariatric surgical procedures have been performed in response to rising obesity rates. However, data on the ass
Externí odkaz:
https://doaj.org/article/32488994cc3a4967a9c94ad4d2c04632
Autor:
Sharif Yassin, Noa Sori, Ophir Gilad, Mati Shnell, Relly Reicher, Nir Bar, Yishai Ron, Nathaniel Aviv Cohen, Subhi Abu-Abeid, Danit Dayan, Shai Meron Eldar, Shira Zelber-Sagi, Sigal Fishman
Publikováno v:
International Journal of Gastrointestinal Intervention, Vol 13, Iss 2, Pp 63-63 (2024)
Externí odkaz:
https://doaj.org/article/bb0afb3c0a1c4001aa509b774fa7b469
Autor:
Ophir Gilad, Guy Rosner, Dana Ivancovsky-Wajcman, Reut Zur, Rina Rosin-Arbesfeld, Nathan Gluck, Hana Strul, Dana Lehavi, Vivien Rolfe, Revital Kariv
Publikováno v:
Genes, Vol 13, Iss 12, p 2182 (2022)
Several studies have demonstrated that curcumin can cause the regression of polyps in familial adenomatous polyposis (FAP), while others have shown negative results. Wholistic turmeric (WT) containing curcumin and additional bioactive compounds may c
Externí odkaz:
https://doaj.org/article/5f07d28de4b346358a146a4a151b4742
Autor:
Guy Rosner, Yael Petel-Galil, Ido Laish, Zohar Levi, Revital Kariv, Hana Strul, Ophir Gilad, Nathan Gluck
Publikováno v:
Clinical and translational gastroenterology. 13(10)
Variants in SMAD4 or BMPR1A cause juvenile polyposis syndrome, a rare autosomal dominant condition characterized by multiple gastrointestinal hamartomatous polyps. A phenotype of attenuated adenomatous polyposis without hamartomatous polyps is rare.W
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Adenomatous polyposis syndromes (APS) patients with ileal pouch anal anastomosis (IPAA) suffer frequent symptoms with scarce signs of inflammation, distinct from ulcerative colitis patients. While the management of pouchitis in ulcerative
Akademický článek
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Autor:
Guy Rosner, Ophir Gilad, Naomi Fliss-Isakov, Sivan Aharon-Kaspi, Revital Kariv, Nathan Gluck, Hana Strul
Publikováno v:
Clinical and Translational Gastroenterology
Introduction Hamartomatous polyposis syndromes (HPS) are rare autosomal-dominant inherited disorders associated with gastrointestinal (GI) tract and other cancers. HPS include Peutz-Jeghers syndrome (PJS), juvenile polyposis syndrome (JPS), and phosp
Publikováno v:
Clinical and Translational Gastroenterology
INTRODUCTION: Total proctocolectomy with ileal pouch anal anastomosis (IPAA) is performed in patients with adenomatous polyposis syndromes (APSs). Data regarding pouch outcomes in APS are scarce. The purposes of this study were to determine the preva
Autor:
Ophir Gilad, Hana Strul, Guy Rosner, Nathan Gluck, Naomi Fliss-Isacov, Joseph Klausner, Ido Wolf, Ofer Merimsky, Yael Goldberg, Zohar Levi, Alona Zer, Revital Kariv
Publikováno v:
Journal of Clinical Oncology. 39:e23544-e23544
e23544 Background: Abdominal desmoid tumors are locally aggressive, non-metastatic tumors that develop mainly in Familial adenomatous polyposis (FAP) patients, within the mesentery or abdominal wall. Understanding and implications of treatment regime
Autor:
Ophir Gilad, Adam Phillips, Sharon Levy, Nir Lubetsky, Yakov Goihkman, Ido Nachmani, Oren Shibolet, Helena Katchman
Publikováno v:
Journal of Hepatology. 73:S263