Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Hazzaa, Alzahrani"'
Autor:
Abdulrahman Al Raizah, Fakhr Alayoubi, Galal Hassan Abdelnaby, Hazzaa Alzahrani, Majid Farraj Bakheet, Mohammed A Alskaini, Rasha Buhumaid, Sameer Al Awadhi, Sara Nooruddin Kazim, Thiagarajan Jaiganesh, Zohair Al Asiri
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)
Background: The non-vitamin K antagonist oral anticoagulants (NOACs) have become the mainstay anticoagulation therapy for patients requiring oral anticoagulants (OACs) in the Gulf Council Cooperation (GCC) countries. The frequency of NOAC-associated
Externí odkaz:
https://doaj.org/article/d198c39d166c4dd699ec2815659eaeeb
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:
Alfadil Haroon, Riad El Fakih, Mahmoud Aljurf, Mohammed Isam Sharif, Tusneem Elhassan, Hazzaa Alzahrani
Publikováno v:
HemaSphere, Vol 7, p e73977c2 (2023)
Externí odkaz:
https://doaj.org/article/146da8c98aa84417892275642c997494
Autor:
Tarek Owaidah MD, Salwa Bakr MD, Nouf Al-Numair PhD, Hala AbaAlkhail PhD, Hazzaa Alzahrani MD, Mahasen Saleh MD, Haitham Khogeer MD, Ahmed Tarawah MD, Hadeel Akkad MD, Faisal Al-Allaf PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 29 (2023)
Establishing a national screening program for hemophilia patients is highly encouraged by the World Health Organization and the World Federation of Hemophilia. Hence, this study aimed to analyze the variant spectrum of F8 and F9 genes in Arab hemophi
Externí odkaz:
https://doaj.org/article/a915efd2ecf849689c48cc1393e88a04
Autor:
Momen Nassani, Riad El Fakih, Jakob Passweg, Simone Cesaro, Hazzaa Alzahrani, Ali Alahmari, Carmem Bonfim, Raheel Iftikhar, Amal Albeihany, Constantijn Halkes, Syed Osman Ahmed, Carlo Dufour, Mahmoud Aljurf
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Bone marrow failure syndromes are a heterogeneous group of diseases. With the major advancements in diagnostic tools and sequencing techniques, these diseases may be better classified and therapies may be further tailored. Androgens, a historic group
Externí odkaz:
https://doaj.org/article/363959dddb5e4c4fa7b577fd2a7253ad
Autor:
Ayman AlHejazi, Amal AlBeihany, Hani AlHashmi, Hazzaa Alzahrani, Ibraheem H Motabi, Ihab El-Hemaidi, Khalid Alsaleh, Khaled El Tayeb, Magdy Rabea, Mohamed Khallaf, Mohammad Hasan Qari
Publikováno v:
Journal of Applied Hematology, Vol 13, Iss 3, Pp 111-117 (2022)
Acquired thrombotic thrombocytopenic purpura (aTTP) is a life-threatening microangiopathy usually characterized by microangiopathic hemolytic anemic, thrombocytopenia, and end-organ ischemia associated with disseminated microvascular platelet-rich th
Externí odkaz:
https://doaj.org/article/d7d943ede7514eeea9741445549c181b
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S29-S30 (2022)
Introduction: Factor X (FX) deficiency is an autosomal recessive disorder caused by quantitative or qualitative defects in the FX protein. FX deficiency has an estimated worldwide prevalence of one in 1000000. (1) Pregnancy in women with congenital F
Externí odkaz:
https://doaj.org/article/90f3affbf68b4ea2912149123a089b73
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:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S40-S41 (2021)
Acquired FXIII deficiency has been described in association with malignancies or autoimmune disorders. We report two cases of acquired FXIII deficiency associated with hematologic malignancies. The first patient is a 60-year-old male with CMML who pr
Externí odkaz:
https://doaj.org/article/d9d562f0173246d1a888b085e6744707
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