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Hematology (Amsterdam, Netherlands)|September 14, 2007
Rapid transformation of atypical myeloproliferative disorder with consistent t(8;13) to B-cell acute lymphoblastic leukemia: a case reportFahri Sahin, Zeynep Sercan, Yesim Ertan, et al.
Hematology (Amsterdam, Netherlands)|September 14, 2007
Multidrug resistance inhibition by antisense oligonucleotide against MDR1/mRNA in P-glycoprotein expressing leukemic cellsFatemeh Nadali, Ali-Akbar Pourfathollah, Kamran Alimoghaddam, et al.
Hematology (Amsterdam, Netherlands)|September 14, 2007
Therapeutic evaluation and prognostic value of interim hybrid PET/CT with (18)F-FDG after three to four cycles of chemotherapy in non-Hodgkin's lymphomaJinhua Zhao, Wenli Qiao, Chun Wang, et al.
Hematology (Amsterdam, Netherlands)|November 26, 2016
GSTT1 (rs4025935) null genotype is associated with increased risk of sickle cell disease in the populations of Tabuk-Northwestern region of Saudi ArabiaFaisel Abu-Duhier, Rashid Mir
Hematology (Amsterdam, Netherlands)|December 2, 2016
HLA-mismatched haploidentical transplantation using low-dose anti-thymocyte globulin (ATG: thymoglobulin)Shinichi Kako, Yu Akahoshi, Naonori Harada, et al.
Hematology (Amsterdam, Netherlands)|April 10, 2023
A review of treatment options employed in relapsed/refractory AMLMohamed Zakee Mohamed Jiffry, Robert Kloss, Mohammad Ahmed-Khan, et al.
Hematology (Amsterdam, Netherlands)|July 8, 2020
Comprehensive screening for coexisting heterozygous α0-thalassemia in hemoglobin E traitChantana Polprasert, Piroonrut Wongprachar, Amornchai Suksusut, et al.
Hematology (Amsterdam, Netherlands)|July 29, 2020
Analysis of rare thalassemia caused by HS-40 regulatory site deletionShiqiang Luo, Xingyuan Chen, Qingyan Zhong, et al.
Hematology (Amsterdam, Netherlands)|March 12, 2015
Role of blood and bone marrow examination in the diagnosis of mature lymphoid neoplasms in patients presenting with isolated splenomegalySreejesh Sreedharanunni, Man Updesh Singh Sachdeva, Pankaj Malhotra, et al.
Hematology (Amsterdam, Netherlands)|August 19, 2020
A novel EPB41 p.Trp704* mutation in a Korean patient with hereditary elliptocytosis: a case reportSoyoung Shin, Kyung-Ah Hwang, Kyuhyun Paik, et al.
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