Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Manik Gemilyan"'
Autor:
Daniil Shauer, Ofelya Petrosyan, Manik Gemilyan, Edward M. Kamau, Pruthu Thekkur, Olga Goncharova, Kalmambetova Gulmira, Bolot Kyrbashov, Kylychbek Istamov, Meder Kadyrov, Ewan Wilkinson
Publikováno v:
Tropical Medicine and Infectious Disease, Vol 8, Iss 8, p 416 (2023)
This study evaluated the effectiveness of an electronic system for managing individuals with drug-sensitive pulmonary tuberculosis in the Kyrgyz Republic. This cohort study used programmatic data. The study included people registered on the paper-bas
Externí odkaz:
https://doaj.org/article/8bcdb6c902bb42ffb033f8131bcc2418
Autor:
Manik Gemilyan, Gagik Hakobyan, Lucie Benejat, Bujana Allushi, Davit Melik-Nubaryan, Harutyun Mangoyan, Amandine Laur, Emilie Daguerre, Eduard Grigoryan, Francis Megraud
Publikováno v:
Gut Pathogens, Vol 11, Iss 1, Pp 1-4 (2019)
Abstract Background The prevalence of Helicobacter pylori infection was never assessed in Armenia, nor was the prevalence of H. pylori resistance against the main antibiotics concerned, despite the fact that these data are fundamental to establish ev
Externí odkaz:
https://doaj.org/article/a0019a437c5a41d99d0e0e3e641d90f7
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Abstract Background Familial Mediterranean fever is an autosomal recessive disorder characterized by periodic febrile attacks of aseptic serositis and/or arthritis. The main treatment is colchicine which prevents attacks in the majority of patients e
Externí odkaz:
https://doaj.org/article/5b7a373e9a594100be3dcc0fa7a5fdf9
Autor:
Peter Katelaris, Richard Hunt, Franco Bazzoli, Henry Cohen, Kwong Ming Fock, Manik Gemilyan, Peter Malfertheiner, Francis Mégraud, Alejandro Piscoya, Duc Quach, Nimish Vakil, Louis G. Vaz Coelho, Anton LeMair, Jim Melberg
Publikováno v:
Journal of clinical gastroenterology. 57(2)
Helicobacter pylori remains a major health problem worldwide, causing considerable morbidity and mortality due to peptic ulcer disease and gastric cancer. The burden of disease falls disproportionally on less well-resourced populations. As with most
Autor:
Elena Baghdasaryan, Tigran Poghosyan, Hayk Hovhannisyan, Gagik Hakobyan, Suren Agho Stepanyan, Karen Manukyan, Manik Gemilyan, Hayk Safaryan
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Most intrahepatic arterioportal fistulae (IAPF) are acquired. The few cases of congenital fistulae are diagnosed in infants and children. CASE SUMMARY We report a 31-year-old female patient presenting with haematemesis and melena three wee
Autor:
Armine, Tumanyan1 (AUTHOR), Manik, Gemilyan2 (AUTHOR), Eduard, Hambartsoumian1 (AUTHOR) Hambartsoumiane@mail.ru
Publikováno v:
Gynecological Endocrinology. 2019 Supplement, Vol. 35, p11-14. 4p.
Autor:
Eduard Grigoryan, Gagik Hakobyan, Davit Melik-Nubaryan, Harutyun Mangoyan, Amandine Marine Laur, Lucie Bénéjat, Francis Mégraud, Bujana Allushi, Emilie Daguerre, Manik Gemilyan
Publikováno v:
Gut Pathogens, Vol 11, Iss 1, Pp 1-4 (2019)
Background The prevalence of Helicobacter pylori infection was never assessed in Armenia, nor was the prevalence of H. pylori resistance against the main antibiotics concerned, despite the fact that these data are fundamental to establish evidence-ba
Autor:
Manik, Gemilyan, Gagik, Hakobyan, Lucie, Benejat, Bujana, Allushi, Davit, Melik-Nubaryan, Harutyun, Mangoyan, Amandine, Laur, Emilie, Daguerre, Eduard, Grigoryan, Francis, Megraud
Publikováno v:
Gut Pathogens
Background The prevalence of Helicobacter pylori infection was never assessed in Armenia, nor was the prevalence of H. pylori resistance against the main antibiotics concerned, despite the fact that these data are fundamental to establish evidence-ba
Controversies surrounding the effect of ES on pregnancy outcome in women with RIF are mostly due to the poorly defined target population. We evaluated the effect of ES on clinical outcomes in women with strict criteria of RIF before IVF/ICSI. We also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a659c034b4715ea1f136ba9ded76699
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Background Familial Mediterranean fever is an autosomal recessive disorder characterized by periodic febrile attacks of aseptic serositis and/or arthritis. The main treatment is colchicine which prevents attacks in the majority of patients except for