Life-Threatening Severe Thrombocytopenia and Mild Autoimmune Hemolytic Anemia Associated with Brucellosis von Ahmed, Waleed Amsaib M., Ahmed Khalil, Khalid, Azwari, Asma, Ebid, Gamal T. A., Nazir, Imran, Aly, Mohamed Hassan

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Corrigendum to “Life-Threatening Severe Thrombocytopenia and Mild Autoimmune Hemolytic Anemia Associated with Brucellosis” von Ahmed, Waleed Amsaib M., Khalil, Khalid Ahmed, Azwari, Asma, Ebid, Gamal T. A., Nazir, Imran, Aly, Mohamed Hassan

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N-Acetyltransferase 2 (NAT2) polymorphism as a risk modifier of susceptibility to pediatric acute lymphoblastic leukemia von Kamel, Azza M., Ebid, Gamal T. A., Moussa, Heba S.

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Association of insulin gene VNTR INS -23/Hph1 A>T (rs689) polymorphism with type 1 diabetes mellitus in Egyptian children von Kamel, Azza M, Mira, Marwa F, Ebid, Gamal T. A, Kassem, Samar H, Radwan, Eman R, Mamdouh, Mona, Amin, Maha, Badawy, Nora, Bazaraa, Hafez, Ibrahim, Amani, Salah, Nermine

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The impact of cytokine gene polymorphisms on the outcome of HLA matched sibling hematopoietic stem cell transplantation von Kamel, Azza M., Gameel, Abdallah, Ebid, Gamal T.A., Radwan, Eman R., Mohammed Saleh, Mostafa F., Abdelfattah, Raafat

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Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia von SHERBORNE, Amy L, HEMMINKI, Kari, KRAJINOVIC, Maja, HEALY, Jasmine, LANCIOTTI, Marina, DUFOUR, Carlo, INDACO, Stefania, EL-GHOUROURY, Eman A, SAWANGPANICH, Ruchchadol, HONGENG, Suradej, PAKAKASAMA, Samart, GONZALEZ-NEIRA, Anna, KUMAR, Rajiv, UGARTE, Evelia L, LEAL, Valeria P, ESPINOZA, Juan P. M, KAMEL, Azza M, EBID, Gamal T. A, RADWAN, Eman R, YALIN, Serap, YALIN, Erdinc, BERKOZ, Mehmet, SIMPSON, Jill, BARTRAM, Claus R, ROMAN, Eve, LIGHTFOOT, Tracy, HOSKING, Fay J, VIJAYAKRISHNAN, Jayaram, GREAVES, Mel, HOULSTON, Richard S, STANULLA, Martin, SCHRAPPE, Martin, PETRIDOU, Eleni, SEMSEI, Agnes F, SZALAI, Csaba, SINNETT, Daniel

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Association of insulin gene VNTR INS -23/Hph1 AT polymorphism with type 1 diabetes mellitus in Egyptian children von Kamel, Azza M, Mira, Marwa F, Ebid, Gamal T. A, Kassem, Samar H, Radwan, Eman R, Mamdouh, Mona, Amin, Maha

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Impact Of Patient/Donor Cytokine Genotypes On The Development Of Acute Graft Versus Host Disease (aGVHD) After Peripheral Blood Stem Cell Transplantation From An Identical Sibling von Kamel, Azza M, Ebid, Gamal TA, Gamil, Abdullah, El-Fattah Raafat, Abd, Mahmoud, Hossam K, El-Mooti, Mohammed Abd

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Lack of association of CTLA-4 +49 A/G polymorphism with predisposition to type 1 diabetes in a cohort of Egyptian families von Kamel, Azza M., Mira, Marwa F., Mossallam, Ghada I., Ebid, Gamal T.A., Radwan, Eman R., Aly Eldin, Nelly H., Mamdouh, Mona, Amin, Maha, Badawy, Nora, Bazaraa, Hafez, Ibrahim, Amani, Salah, Nermine, Hansen, John

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The possible correlation between miR-762, Hippo signaling pathway, TWIST1, and SMAD3 in lung cancer and chronic inflammatory diseases von Hussein, Neveen A., Ebid, Samia A., Ahmad, Mohammad A., Khedr, Gamal E., Saad, Dina M.

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Association of methylenetetrahydrofolate reductase (MTHFR) C677T, MTHFR A1298C, and CYP3A4 A290G gene polymorphisms with clinical outcomes of HLA-matched sibling allogeneic hematop... von ElFishawi, Sally, Abdelfattah, Raafat, Radwan, Eman R., Rasekh, Eman O, Mohammed Saleh, Mostafa F., El-Beih, Essam A., Herdan, Omar M., Ebid, Gamal T., fahmy, Omar, Askar, Medhat Z., Kamel, Azza M.

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Polymorphisms of the DNA repair genes (APE1, XPD, and RAD51) and the risk of developing cytogenetic abnormalities in a cohort of Egyptian patients with newly diagnosed AML von El-Noshokaty, Essam, Ebid, Gamal, Ayoub, Mahmoud, Gawdat, Rania

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The Prevalence and Antimicrobial Susceptibility of Methicillin-Resistant Staphylococcus aureus Before and After the COVID-19 Pandemic in a Tertiary Saudi Hospital von Ahmed, Omar B, Bahwerth, Fayez S, Alsafi, Radi, Elsebaei, Eman A, Ebid, Gamal T, Theyab, Abdulrhaman, Assaggaf, Hamza

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DNMT3A-448AG nucleotide polymorphism and susceptibility to acute myeloid leukemia in a cohort of Egyptian patients von Elnoshokaty, Essam, Ebid, Gamal, Fahmy, Mohamed, Shikhon, Tarek, Gawdat, Rania

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Polymorphisms of the DNA repair genes von El-Noshokaty, Essam, Ebid, Gamal, Ayoub, Mahmoud, Gawdat, Rania

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DNMT3A-448A>G nucleotide polymorphism and susceptibility to acute myeloid leukemia in a cohort of Egyptian patients von Elnoshokaty, Essam, Ebid, Gamal, Fahmy, Mohamed, Shikhon, Tarek, Gawdat, Rania

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Coagulation Profile in COVID-19 Patients and its Relation to Disease Severity and Overall Survival: A Single-Center Study von Abd El-Lateef, Amal Ezzat, Alghamdi, Saad, Ebid, Gamal, Khalil, Khalid, Kabrah, Saeed, Abdel Ghafar, Muhammad Tarek

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Clinical Effect of Combined Mutations in DNMT3A, FLT3-ITD, and NPM1 Among Egyptian Acute Myeloid Leukemia Patients von El Gammal, Mosaad M., Ebid, Gamal T., Madney, Youssef M., Abo-Elazm, Omnia M., Kelany, Ayda K., Torra, Olga S., Radich, Jerald P.

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Prevalence of the frequency of JAK2 (V617F) mutation in different myeloproliferative disorders in Egyptian patients von Ebid, Gamal T, Ghareeb, Mohamed, Salaheldin, Omina, Kamel, Mahmoud M

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Role of CTLA4-49A polymorphism in the pathogenesis of acute leukemia von Hawass, MahmoudA, Afifi, EssamA, Hazaa, IbrahimH.M, Ebid, GamalT.A

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