Výsledky vyhledávání

HLA-identical related hematopoietic stem cell transplantation in severe sickle cell disease: age is not a barrier to successful outcome

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

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Apheresis platelets transfusion from a COVID-19 positive donor in a hematopoietic stem cell transplantation patient-- case report

Autor: Mohammed F. Essa, Enas Basher, Musaed Alharbi, Khalid Batarfi

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

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Outcome of Hematopoietic Stem Cell Transplantation in Children with Primary Hemophagocytic Lymphohistiocytosis: A Single Institution Experience Using Reduced Intensity Conditioning

Autor: Enas Basher, Abdulrahman Alsultan, Mohammed F. Essa, Rodaina Abujoub

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

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Hematopoietic Stem Cell Transplantation in Children with Sickle Cell Disease: Myeloablative Versus Reduced Intensity Conditioning

Autor: Rodaina Abujoub, Enas Basher, Abdulrahman Alsultan, Mohammed F. Essa

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

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Frequency of Veno-Occlusive Disease in Children with B-Thalassemia Major Who Underwent Hematopoietic Stem Cell Transplantation

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

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Outcome of Age-Adapted Approach to HLA-Identical Related Hematopoietic Stem Cell Transplantation in Severe Sickle Cell Disease: Saudi Experience

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

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Deficiency of ADA2 mimicking autoimmune lymphoproliferative syndrome in the absence of livedo reticularis and vasculitis

Autor: Abdulrahman Alsultan, Enas Basher, Majid Alfadhel, Reem Mohammed, Jubran Theeb Alqanatish

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

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