Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Fahad AlMohareb"'
Autor:
Hussain A. BinAmir, Ali AlAhmari, AlWaleed AlQahtani, Gamal Mohamed, Fawaz Alotaibi, Mohamed AlShamrani, Ali AlSaeed, Suwaidi AlGhanmi, Alaa Heji, Abdulrahman Alreshaid, Ammar AlKawi, Adel AlHazzani, Mohamed AlZawahmah, Ashfaq Shuaib, Fahad Al-Ajlan, Fahad AlMohareb
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionPosterior reversible encephalopathy syndrome (PRES) is a serious neurological syndrome that may develop following immunosuppressive therapy for stem cell transplantation (SCT). We report 8 patients with sickle cell disease (SCD) who devel
Externí odkaz:
https://doaj.org/article/4cfee35c3ba44630a71b4741e26f06ae
Autor:
Alfadil Haroon, Syed Osman Ahmed Ahmed, Hazzaa Alzahrani, Riad El Fakih, Ali Alahmari, Alfadel Alshaibani, Naeem Chaudhri, Fahad Almohareb, Saud Alhayli, Marwan Shaheen, Abdulwahab Albabtain, Fahad Alsharif, Feras Alfraih, Walid Rasheed, Mahmoud Aljurf
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S19-S20 (2023)
Objective Background: Aplastic anemia is pancytopenia with a hypocellular bone marrow [
Externí odkaz:
https://doaj.org/article/b7ebc9153dc04124ab792ca949de7f81
Autor:
Samar Alfaqawi, Mostafa Mohammed Saleh, Ahmed Kotb, Ghada Abdallah, Leena Ali, Reem Alasbali, Taimor Hussain, Haroon Alfadhil, Ahmed Bin Salman, Momen Nassani, Yazeed Baujaifer, Mohammed I. Sharif, Marwa Nassar, Sarah Samarkandi, Heba Madien, Amal Hejab, Ruah Alyamany, Ahmed Alnughmush, Abdullah Alamer, Ayman Saad, Mansour Alfayez, Abdelwahab Albabtain, Alfadel Alshaibani, Ahmad Alotaibi, Saud Alhayli, Marwan Shaheen, Syed O. Ahmed, Riad Elfakih, Amr Hanbali, Feras Alfraih, Walid Rasheed, Fahad Alsharif, Naeem Chaudhri, Hazza Alzahrani, Fahad Almohareb, Mahmoud Aljurf, Ali Alahmari
Publikováno v:
HemaSphere, Vol 7, p e06488d6 (2023)
Externí odkaz:
https://doaj.org/article/a0b321b6475b4ca8b1e7c3944e1ad24a
Autor:
Mona Hassanein, Riad El Fakih, Walid Rasheed, Syed Ahmed, Marwan Shaheen, Naeem Chaudhri, Fahad Alsharif, Shad Ahmed, Amr Hanbali, Alfadel AlShaibani, Feras Alfraih, Saud Alhayli, Tusneem Elhassan, Ali Alahmari, Hazzaa Alzahrani, Fahad Almohareb, Mahmoud Aljurf, Shahrukh Hashmi
Publikováno v:
eJHaem, Vol 2, Iss 2, Pp 249-256 (2021)
Abstract Secondary acute myeloid leukemia (sAML) includes AML as a complication of an antecedent hematological disorder or a therapy‐related AML. Large registry‐based data identified sAML as an independent poor‐outcome type of AML post allogene
Externí odkaz:
https://doaj.org/article/c864142de1904dff964406052a91be60
Publikováno v:
Blood Advances, Vol 4, Iss 1, Pp 229-238 (2020)
Abstract: Acute myeloid leukemia (AML) with t(8;21)(q22;q22.1);RUNX1-RUNX1T1, one of the core-binding factor leukemias, is one of the most common subtypes of AML with recurrent genetic abnormalities and is associated with a favorable outcome. The tra
Externí odkaz:
https://doaj.org/article/f58f95da71a84a558df7b318ca597a6f
Autor:
Majed Dasouki, Ayodeele Alaiya, Tanziel ElAmin, Zakia Shinwari, Dorota Monies, Mohamed Abouelhoda, Amjad Jabaan, Feras Almourfi, Zuhair Rahbeeni, Fahad Alsohaibani, Fahad Almohareb, Hazzaa Al-Zahrani, Francisco J. Guzmán Vega, Stefan T. Arold, Mahmoud Aljurf, Syed Osman Ahmed
Publikováno v:
iScience, Vol 24, Iss 3, Pp 102214- (2021)
Summary: Autosomal recessive mutations in G6PC3 cause isolated and syndromic congenital neutropenia which includes congenital heart disease and atypical inflammatory bowel disease (IBD). In a highly consanguineous pedigree with novel mutations in G6P
Externí odkaz:
https://doaj.org/article/e70cc78710c248be86f58e5e90251a2b
Autor:
Amr Hanbali, Ahmed Kotb, Riad El Fakih, Feras Alfraih, Syed Osman Ahmed, Marwan Shaheen, Saud Alhayli, Ali Alahmari, Ahmad Alotaibi, Alfadel Alshaibani, Mahmoud Abu Riash, Farah Deeba, Maryam Asif, Walid Rasheed, Hazzaa Alzahrani, Fahad Alsharif, Naeem Chaudhri, Fahad Almohareb, Mahmoud Aljurf
Publikováno v:
Leukemia Research Reports, Vol 16, Iss , Pp 100270- (2021)
Background: Treating adolescents and young adults (AYA) patients with acute lymphoblastic leukemia (ALL) using pediatric-inspired protocols have shown improvement in outcomes. Most data available in the literature of such protocols is derived from we
Externí odkaz:
https://doaj.org/article/0920ff50755a4213b57bcd981e064517
Autor:
Barbara Cappelli, Fernanda Volt, Karina Tozatto-Maio, Graziana Maria Scigliuolo, Alina Ferster, Sophie Dupont, Belinda Pinto Simões, Amal Al-Seraihy, Mahmoud D. Aljurf, Fahad Almohareb, Cristina Belendez, Susanne Matthes, Nathalie Dhedin, Corinne Pondarre, Jean-Hugues Dalle, Yves Bertrand, Jean Pierre Vannier, Mathieu Kuentz, Patrick Lutz, Gérard Michel, Hanadi Rafii, Benedicte Neven, Marco Zecca, Peter Bader, Marina Cavazzana, Myriam Labopin, Franco Locatelli, Alessandra Magnani, Annalisa Ruggeri, Vanderson Rocha, Françoise Bernaudin, Josu de La Fuente, Selim Corbacioglu, Eliane Gluckman
Publikováno v:
Haematologica, Vol 104, Iss 12 (2019)
Externí odkaz:
https://doaj.org/article/37740344a46448c0bc25c6ada08b8d41
Autor:
Riad El Fakih, Rayid Abdulqawi, Amer Bugnah, Tarek Arabi, Walid Rasheed, Loui Ezzat, Marwan Shaheen, Naeem Chaudhri, Fahad Almohareb, Eid Al Mutairy, Mahmoud D Aljurf
Introduction: Severe pulmonary GvHD after allo-HCT is a significant cause of morbidity and mortality with limited therapeutic options. Selected patients can be lung transplanted, however there are no consensus guidelines on whom to select nor on when
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5722534a6c29998f6a05237f1b198cd
https://doi.org/10.21203/rs.3.rs-2890159/v1
https://doi.org/10.21203/rs.3.rs-2890159/v1
Autor:
Said Dermime, Mahmoud Aljurf, Abdelghani Tbakhi, Hazza Al-Zahrani, Fahad Alsharif, Naeem Chaudhri, Fahad Almohareb, Khaled Al-Hussein, Ghofran Al Qudaihi, Abdullah Al-Sulaiman, Hazem Ghebeh, Cynthia Lehe
Supplement 1 from The Wilms' Tumor Antigen Is a Novel Target for Human CD4+ Regulatory T Cells: Implications for Immunotherapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39199304bc948f43fdd51687bd405417
https://doi.org/10.1158/0008-5472.22374878
https://doi.org/10.1158/0008-5472.22374878