Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Fahed Almhareb"'
Autor:
Abdul Kareem Almomen, Abdul Ghani Al Bakistani, Ahmad Alsaeed, Asma Al Olama, Ayman Hejazi, Christian Awarji, Fahed Almhareb, Faisal Alsayegh, Hazzaa Alzahrani, Mahmoud Almarashly, Mohammad Qari, Mohammad Aslam, Rania Seliem, Salam Al Kindi, Saud Abuharbesh, TareK Owaidah, Wafaa Bassuni
Publikováno v:
Journal of Applied Hematology, Vol 5, Iss 2, Pp 37-44 (2014)
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired, rare clonal blood disorder, characterized by chronic intravascular hemolysis, bone marrow failure, renal failure and pulmonary hypertension, and a heightened risk of thrombotic complications.
Externí odkaz:
https://doaj.org/article/1d3ae7270fca4498a20fca0b3ea5edee
Autor:
Jim A. Connelly, Eden Biltibo, Karina Wilkerson, Adriana Seber, Roseane V Gouveia, Carmem Bonfim, Belinda Pinto Simões, Erfan Nur, Biljana N. Horn, Michael Eckrich, Rabi Hanna, Nathalie Dhedin, Fahed Almhareb, Mahmoud Aljurf, Hemalatha G. Rangarajan, Katie S. Gatwood, Lindsay Orton, Carrie Lynn Kitko, Mohsen Alzahrani, Ali Debsan Alahmari, Josu De La Fuente, Adetola A. Kassim
Publikováno v:
Blood. 140:10462-10464
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abee17870acc0f0e408d86e365788114
https://doi.org/10.1182/blood-2022-170552
https://doi.org/10.1182/blood-2022-170552
Autor:
Adetola A. Kassim, Karina Wilkerson, Josu de la Fuente, Adriana Seber, Roseane V Gouveia, Carmem Bonfim, Belinda Pinto Simões, Erfan Nur, Biljana N. Horn, Michael Eckrich, Rabi Hanna, Nathalie Dhedin, Fahed Almhareb, Mahmoud Aljurf, Hemalatha G. Rangarajan, Katie S. Gatwood, James P Connelly, Mohsen Alzahrani, Ali Alahmari, Mark Rodeghier, Michael R. DeBaun
Publikováno v:
Blood. 140:2383-2385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::341d9168400de6fc71a2b10525448055
https://doi.org/10.1182/blood-2022-165229
https://doi.org/10.1182/blood-2022-165229
Autor:
Ahmed Bin Salman, Syed O. Ahmed, Saleha abdul Rab, Hiba Raheel, Areez Shafqat, Saud Alhayli, Alfadel Alshaibani, Naeem A. Chaudhri, Abdulwahab Albabtain, Feras Abdulaziz Alfraih, Mansour Alfayez, Fahad Alsharif, Marwan Shaheen, Amr Suleiman Hanbali, Ahmad S. Alotaibi, Walid Rasheed, Fahed Almhareb, Ali Alahmari, Hazza Alzahrani, Mahmoud Aljurf, Riad El Fakih
Publikováno v:
Blood. 140:12969-12970
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faf2d28a2fff04631e6b66e7c088fd0c
https://doi.org/10.1182/blood-2022-164820
https://doi.org/10.1182/blood-2022-164820
Autor:
Ali Alsugair, Syed O. Ahmed, Mohamed Isam Sharif, Tusneem Elhassan, Hazza A. Alzahrani, Fahed Almhareb, Naeem A. Chaudhri, Fahad Alsharif, Walid Rasheed, Amr Hanbali, Feras Abdulaziz Alfraih, Marwan Shaheen, Riad El Fakih, Saud Alhayli, Ali Alahmari, Alfadel Alshaibani, Abdulwahab Albabtain, Ahmad S. Alotaibi, Mansour Alfayez, Mahmoud Aljurf
Publikováno v:
Blood. 140:10566-10567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::299a52529044b7ef90d1acd1d7d45d65
https://doi.org/10.1182/blood-2022-167509
https://doi.org/10.1182/blood-2022-167509
Autor:
Ahmad S. Alotaibi, Shad Ahmed, Walid Rasheed, Marwan Shaheen, Nadiah Alobaidi, Ahmad Alnughmush, Amal Hejab, Taimoor Hussain, Ahmed Abdrabou, Haroon Alfadhil, Mostafa Saleh, Ahmed Bin Salman, Majed Altareb, Momen Nassani, Yazeed S Bajuaifer, Mohamed Isam Sharif, Emad Ghabashi, Shaykhah Alotaibi, Riad Youniss, Alfadel Alshaibani, Ali Alahmari, Saud Alhayli, Riad Elfakih, Feras Al Fraih, Amr Suleiman Hanbali, Fahad Alsharif, Naeem A. Chaudhri, Hazza Alzahrani, Fahed Almhareb, Mahmoud Aljurf, Syed O. Ahmed
Publikováno v:
Blood. 138:1851-1851
Background A significant proportion of patients with acute myeloid leukemia (AML) will either be refractory to initial chemotherapy or will suffer refractory relapse. The role of allogeneic transplantation (SCT) in active disease is contentious. Ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643e64eb25d241227b0adea304823ae1
https://doi.org/10.1182/blood-2021-152602
https://doi.org/10.1182/blood-2021-152602
Autor:
Marwan Shaheen, Amr Hanbali, Mahmoud Aljurf, Hazza A Alzahrani, Riad Elfakih, Fahed Almhareb, Tarek Owaidah, Shahrukh K. Hashmi, Fahad Alsharif, Zakia Shinwari, Naeem Chaudhri, Syed Osman Ahmed, Feras Al Fraih, Walid Rasheed, Ayodele Alaiya, Saud Alhayli
Publikováno v:
Blood. 132:5434-5434
Clinical and molecular diagnosis of most hematological malignancies including Chronic Myeloid Leukemia (CML) can be accurately made. However, prediction of treatment response and estimation of disease survival period eludes the currently available to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::810096239e10036f67133442e17ea550
https://doi.org/10.1182/blood-2018-99-118754
https://doi.org/10.1182/blood-2018-99-118754
Autor:
Naeem Chaudhri, Mahmoud Aljurf, Syed Osman Ahmed, Claudia Ulrike Walter, Amr Nassar, Mohammad Bakr, Abu Jafar Saleh, Fahed Almhareb, Hazzaa Alzahrani
Publikováno v:
Hematology/Oncology and Stem Cell Therapy, Vol 2, Iss 3, Pp 399-402 (2009)
Acute lymphoblastic leukemia (ALL) is a relatively rare disease during pregnancy, accounting for about 15% of all cases of pregnancy-associated leukemia. Although mixed lineage leukemia gene (MLL) rearrangement is the dominant genetic aberration in i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06a8d05685e040e311bf517d1e46b723
http://www.sciencedirect.com/science/article/pii/S1658387609500088
http://www.sciencedirect.com/science/article/pii/S1658387609500088
Autor:
Hazza A Alzahrani, Amna Gamil, Naeem Chaudhri, Mahmoud Aljurf, Muhamad Hitham Almahayni, Walid Rasheed, Shad Ahmed, Khaled Ibrahim, Ghuzayel Aldawsari, Marwan Shaheen, Fahad Alsharif, Feras Alfraih, Syed Osman Ahmed, Said Y Mohamad, Fahed Almhareb, Amr Hanbali
Publikováno v:
Blood. 126:5482-5482
A Significant Proportion of Young Adult Patients with Post -HCT Relapse Of AML Benefit From Aggressive Salvage And 2nd Cellular Therapy. INTRODUCTION: There is currently no standard of care for patients with AML who relapse following hematopoietic ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::789c59203fc7ae0c693d7e8ad4fbd924
https://doi.org/10.1182/blood.v126.23.5482.5482
https://doi.org/10.1182/blood.v126.23.5482.5482
Autor:
Salam Al Kindi, Hazzaa Alzahrani, Mohammad Qari, Fahed Almhareb, Tarek Owaidah, Asma Al Olama, Abdulkareem Al-Momen, Saud Abuharbesh, Mahmoud Almarashly, Ayman Hejazi, Christian Awarji, Mohammad Aslam, Faisal Alsayegh, Ahmad Alsaeed, Wafaa Bassuni, Rania M. Seliem, Abdul Ghani Al Bakistani
Publikováno v:
Journal of Applied Hematology, Vol 5, Iss 2, Pp 37-44 (2014)
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired, rare clonal blood disorder, characterized by chronic intravascular hemolysis, bone marrow failure, renal failure and pulmonary hypertension, and a heightened risk of thrombotic complications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::644342a2585438357ade9fb471c2551a
https://doi.org/10.4103/1658-5127.137081
https://doi.org/10.4103/1658-5127.137081