Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Enas Basher"'
Autor:
Mohsen Alzahrani, Samer Ghazi, Ayman Hejazi, Abdulrahman Alsultan, Giamal Gmati, Khadega A. Abuelgasim, Hind Salama, Rodaina Abujoub, Mohammed Sh. Essa, Heba Alshobaki, Enas Basher, Husam Mazin Alsadi, Mazin Ahmed, Bader Alahmari, Moussab Damlaj, Ahmed Alaskar
Publikováno v:
Bone marrow transplantation. 57(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21da874880c8b0035bfb453e0d815f31
https://pubmed.ncbi.nlm.nih.gov/34743184
https://pubmed.ncbi.nlm.nih.gov/34743184
Coronavirus pandemic is the present concern worldwide. The virus is transmitted via a droplet route; however, transmission through blood products had not been reported. We present a 22-month-old boy with leukemia who developed fever and liver veno-oc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e6ef27d1184110eeb4767fc257bcd7e
https://doi.org/10.22541/au.159359235.55717503
https://doi.org/10.22541/au.159359235.55717503
Publikováno v:
Blood. 136:43-44
Hematopoietic stem cell transplantation (HSCT) is the only curative therapy for primary hemophagocytic lymphohistiocytosis (HLH). Conventional myeloablative conditioning regimen using busulfan, cyclophosphamide with or without etoposide was associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b9ea784bad2ad4cebf64bbaa2ebe370
https://doi.org/10.1182/blood-2020-142988
https://doi.org/10.1182/blood-2020-142988
Publikováno v:
Biology of Blood and Marrow Transplantation. 26:S222-S223
Background Sickle cell disease (SCD) is prevalent in Saudi Arabia. We reviewed transplant outcome among SCD patients who underwent HLA-matched related donor HSCT at our institution using either myeloablative or reduced intensity conditioning (RIC) Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbc5fa19b381979c2760064c66cdce8e
https://doi.org/10.1016/j.bbmt.2019.12.542
https://doi.org/10.1016/j.bbmt.2019.12.542
Autor:
Reem Al Sudairy, Ali Alomari, Talal Alharbi, Khaled Aljamaan, Mohammed F. Essa, Abdulrahman Alsultan, Enas Basher
Publikováno v:
Biology of Blood and Marrow Transplantation. 24:S441-S442
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0b3eafd8a96860e03df28bd61d45f16
https://doi.org/10.1016/j.bbmt.2017.12.533
https://doi.org/10.1016/j.bbmt.2017.12.533
Autor:
Ahmed Alaskar, Giamal Gmati, Hind Salama, Mohsen Alzahrani, Khadega A. Abuelgasim, Abdulrahman Alsultan, Ayman Hejazi, Rodaina Abujoub, Bader Alahmari, Enas Basher, Samer Ghazi, Moussab Damlaj, Mohammed F. Essa
Publikováno v:
Blood. 132:3468-3468
Sickle cell disease (SCD) is one of the most common inherited disorders in Saudi Arabia with nearly 60,000 affected individuals (Alsultan et al. Ped. Transplant. 2016). Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21cf53633e8528e11f7b21e0ab65e615
https://doi.org/10.1182/blood-2018-99-115800
https://doi.org/10.1182/blood-2018-99-115800
Publikováno v:
Pediatric Blood & Cancer. 65:e26912
Adenosine deaminase-2 (ADA2) deficiency (DADA2) is associated with early onset polyarteritis nodosa and vasculopathy. Classic presentation includes livedo reticularis, vasculitis, and stroke. However, the phenotype and disease severity are variable.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c53e965ab7e501e8acb7425cff0c057
https://doi.org/10.1002/pbc.26912
https://doi.org/10.1002/pbc.26912
Publikováno v:
Pediatric Blood & Cancer; Apr2018, Vol. 65 Issue 4, p1-1, 4p