Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ali M. Assiri"'
Publikováno v:
Leukemia Research Reports, Vol 14, Iss , Pp 100220- (2020)
Pro-myelocytic acute leukemia (APL) is characterized by the proliferation of cells blocked at promyelocytic stage and ATRA is the choice of initial treatment because of the APL sensitivity to this compound. In this case study we report a 28-year-old
Externí odkaz:
https://doaj.org/article/0e07049d2efe4ee8b66bca726abfd138
Autor:
Tusneem Elhassan, Alfadel Alshaibani, Riad El Fakih, Anas Alhakim, Hazzaa Alzahrani, Fahad Alsharif, Fahad Almohareb, Emad Ghabashi, Ahmed Balbaid, Fatima Babiker, Ahmad Alshomar, Mahmoud Aljurf, Naeem Chaudhri, Husam Alsadi, Ahmed Kotb, Syed Osman Ahmed, Walid Rasheed, Saud Alhayli, Amr Hanbali, Ali M. Assiri, Ali Al-Ahmari, Feras Alfraih, Marwan Shaheen, Hadeel Samarkandi
Publikováno v:
Transplantation and cellular therapy. 27(10)
The recommended therapy for severe aplastic anemia (SAA) in younger patients with a matched sibling donor (MSD) is allogeneic hematopoietic cell transplantation (allo-HCT). A number of conditioning regimens and protocols have been used for these pati
Publikováno v:
Leukemia Research Reports, Vol 14, Iss, Pp 100220-(2020)
Leukemia Research Reports
Leukemia Research Reports
Pro-myelocytic acute leukemia (APL) is characterized by the proliferation of cells blocked at promyelocytic stage and ATRA is the choice of initial treatment because of the APL sensitivity to this compound. In this case study we report a 28-year-old
Publikováno v:
European Journal of Molecular and Clinical Medicine, Vol 5, Iss 1, Pp 37-40 (2018)
Evans syndrome is a rare autoimmune disorder with an unknown etiology. In this paper, we report the case of a 32-year-old Saudi woman living with Evans syndrome for more than 8 years (post-splenectomy) who was also diagnosed with systemic lupus eryth
Autor:
Daniel M. Griffith, Kimberly A. Casey, Florian M. Schwandner, Frank E. Muller-Karger, Vincent Realmuto, Christopher R. Hakkenberg, Qingyuan Zhang, Philip E. Dennison, J. L. Torres-Perez, Dar A. Roberts, Thomas R. H. Holmes, Alexey N. Shiklomanov, Robert Frouin, Maria Fabrizia Buongiorno, Nima Pahlevan, Hamid Dashti, Roberta E. Martin, Christine Lee, Fabian D. Schneider, Kyla M. Dahlin, Chuanmin Hu, Yi Qi, Pamela L. Blake, Ali M. Assiri, Yusri Yusup, Michael E. Schaepman, Kevin R. Turpie, Nimrod Carmon, Adam Erickson, David S. Schimel, Joseph D. Ortiz, Nancy F. Glenn, Michelle M. Gierach, Maria Tzortziou, Susan L. Ustin, Hamed Gholizadeh, Heidi M. Dierssen, David R. Thompson, E. Natasha Stavros, Joshua B. Fisher, Raymond F. Kokaly, D. B. Otis, Petya K. E. Campbell, Kerry Cawse-Nicholson, Philip A. Townsend, Raphael M. Kudela, James A. Goodman, Karl F. Huemmrich, Wesley J. Moses, T. H. Painter, Ben Poulter, Qian Yu, Glynn Hulley, Charles K. Gatebe, Eric J. Hochberg, Ryan Pavlick, Charles E. Miller, Shawn P. Serbin, Liane S. Guild, Rosa Elvira Correa-Pabón
Publikováno v:
Remote Sensing of Environment. 257:112349
The 2017–2027 National Academies' Decadal Survey, Thriving on Our Changing Planet, recommended Surface Biology and Geology (SBG) as a “Designated Targeted Observable” (DO). The SBG DO is based on the need for capabilities to acquire global, hig
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 17(5)
Refractory antiphospholipid syndrome represents a challenge for preventing thrombosis that may occur despite adequate anticoagulation and immunomodulation therapy. Here, we report a 35-year-old male patient who presented with variable venous thromboe
Autor:
Amr Hanbali, Wedian Mustafa Rawas, Tusneem Elhassan, Saud Alhayli, Imad Ghabashi, Mona Hassanein, Riad El Fakih, Fahd Almohareb, Walid Rasheed, Shahrukh K. Hashmi, Ahmed Alshomer, Marwan Shaheen, Hazzaa Alzharani, Anas Alhakim, Feras Alfraih, Naeem Chaudhri, Ali M. Assiri, Ahmed Kotb, Husam Alsadi, Mahmoud Aljurf, Mohammed A. Assiri, Fahad Alsharif, Ahmed Balbaid, Syed Sayeed Ahmed
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 18:S305
Publikováno v:
International Research Journal of Medicine and Medical Sciences.
Pericarditis is a rare but potentially serious comp lication of tuberculosis. The clinical features of Tuberculous pericarditis are often subtle and nonspecific, leading to delayed or missed diagnosis. As a result, patients of Tuberculous pericarditi
Autor:
Ali M. Assiri, Abdullah M. Alshehri, Sabah N. Nemri, Saif Aboud Alqahtani, Mohammed A. Alzahrani
Publikováno v:
The Open Gastroenterology Journal. 6:31-33
Eosinophilic gastroenteritis (EGE) is a rare disease of the gastrointestinal tract characterized by eosinophilic in- filtration of the bowel wall and variable gastrointestinal manifestation. The signs and symptoms of EGE are related to the extent of
Assessment of knowledge, attitude and practice of diabetic people in Najran, Kingdom of Saudi Arabia
Autor:
Mohammed Yahia Alasmary, Abdullah I. Aedh, Ali M. Assiri, Walid G Babikr, Awad Mohamed Ahmed, Ahmed Abdelraheem, Hamdan Alshehri, Amar B. Elhussein, Awad Mohammed Al-Qahtani, Anas R. Alijla, Hatem Mohamed, Abubaker A. Younis, Mutaz M. Ahmed
Publikováno v:
International Journal of Research in Medical Sciences. 5:2150
Background: This cross-sectional hospital based study aimed at determining the level of knowledge, attitude and practice of diabetes among local people of Najran, Saudi Arabia.Methods: We aimed to investigate the levels of knowledge, attitude and pra