- Cord blood 2.0: state of the art and future directions in transplant medicine
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Wagner JE
- KMID: 2451049
- Blood Res.
- 2019 Mar;54(1):7-9.
- doi: 10.5045/br.2019.54.1.7
No abstract available. -
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- Organ-specific considerations for marginal zone lymphomas in Korea, based on Consortium for Improving Survival of Lymphoma (CISL) and Korean clinical studies
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Oh SY, Suh C
- KMID: 2451048
- Blood Res.
- 2019 Mar;54(1):4-6.
- doi: 10.5045/br.2019.54.1.4
No abstract available. -
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- Recurrent bilateral deep vein thrombosis after cava vein resection in a patient with leiomyosarcoma
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Lucia OO, Pablo DR, Sandra PR, Jorge DT
- KMID: 2451045
- Blood Res.
- 2019 Mar;54(1):1-1.
- doi: 10.5045/br.2019.54.1.1
No abstract available. -
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- Hemophagocytosis by blasts in acute lymphoblastic leukemia
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Klein E, Derrieux C, Dulucq S
- KMID: 2451046
- Blood Res.
- 2019 Mar;54(1):2-2.
- doi: 10.5045/br.2019.54.1.2
No abstract available. -
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- Coexistence of BCR/ABL1-positive chronic myeloid leukemia and JAK2 V617F-mutated myelofibrosis successfully treated with dasatinib and ruxolitinib
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Yi JH, Kim HR
- KMID: 2451060
- Blood Res.
- 2019 Mar;54(1):77-79.
- doi: 10.5045/br.2019.54.1.77
No abstract available. -
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- Molecular perspective of iron uptake, related diseases, and treatments
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Shokrgozar N, Golafshan
- KMID: 2451050
- Blood Res.
- 2019 Mar;54(1):10-16.
- doi: 10.5045/br.2019.54.1.10
Iron deficiency anemia and anemia of chronic disorders are the most common types of anemia. Disorders of iron metabolism lead to different clinical scenarios such as iron deficiency anemia, iron... -
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- A case of immune thrombocytopenia associated with invasive thymoma successfully treated with eltrombopag
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Yoon JK, Jang HR, Park JH, Kim KH, Roh EY, Byun JM
- KMID: 2451059
- Blood Res.
- 2019 Mar;54(1):74-79.
- doi: 10.5045/br.2019.54.1.74
No abstract available. -
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- Breast implant-associated anaplastic large cell lymphoma
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Baseggio L, Travers-Glehen A, Bachy E, Laurent C
- KMID: 2451047
- Blood Res.
- 2019 Mar;54(1):3-3.
- doi: 10.5045/br.2019.54.1.3
No abstract available. -
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- Microcytosis in children and adolescents with the sickle cell trait in Basra, Iraq
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Jaber RZ, Hassan MK, Al-Salait
- KMID: 2451054
- Blood Res.
- 2019 Mar;54(1):38-44.
- doi: 10.5045/br.2019.54.1.38
BACKGROUND: Microcytic anemia, the most common form of anemia in children and adolescents, is a heterogeneous group of diseases that is acquired or inherited. We assessed the frequency and causes... -
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- Analysis of hematologic parameters of donors, patients, and granulocyte concentrates to predict successful granulocyte transfusion
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Lee JM, Choi SJ, Kim HS, Yang M, Kim Y, Lee JW, Lim J
- KMID: 2451056
- Blood Res.
- 2019 Mar;54(1):52-56.
- doi: 10.5045/br.2019.54.1.52
BACKGROUND: Granulocyte transfusion (GTx) is performed as a supportive therapy in severe neutropenic patients caused by various conditions. The study aimed to analyze the hematologic parameters of donors, patients, and... -
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- ABCB1 and BMI1 mRNA expression in patients with chronic myeloid leukemia: impact on imatinib efficacy
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Bedewy AM, Elmaghraby SM, Kandil NS
- KMID: 2451057
- Blood Res.
- 2019 Mar;54(1):57-62.
- doi: 10.5045/br.2019.54.1.57
BACKGROUND: ATP-binding cassette transporters are important in the mechanism of multidrug resistance. ABCB1 displays a high affinity for imatinib. BMI1 is a polycomb group protein thought to be overexpressed in... -
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- Biochemical effects and safety of Gum arabic (Acacia Senegal) supplementation in patients with sickle cell anemia
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Kaddam LA, Fdl-Elmula I, Eisawi OA, Abdelrazig HA, Elnimeiri , Saeed AM
- KMID: 2451053
- Blood Res.
- 2019 Mar;54(1):31-37.
- doi: 10.5045/br.2019.54.1.31
BACKGROUND: Sickle cell anemia (SCA) is a hereditary chronic hemolytic anemia with several clinical consequences. Intravascular sickling of red blood cells leads to multi-organ dysfunction. Moreover, several biochemical abnormalities have... -
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- Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology
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Lee YK, Kim HJ, Lee K, Park SH, Song SH, Seong MW, Kim M, Han JY
- KMID: 2451051
- Blood Res.
- 2019 Mar;54(1):17-22.
- doi: 10.5045/br.2019.54.1.17
Genetic hemoglobin disorders are caused by mutations and/or deletions in the α-globin or β-globin genes. Thalassemia is caused by quantitative defects and hemoglobinopathies by structural defect of hemoglobin. The incidence... -
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- Efficacy of parenteral glutamine supplementation in adult hematopoietic stem cell transplantation patients
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Cho YK, Hong SY, Jeon SJ, Namgung HW, Lee E, Lee E, Bang SM
- KMID: 2451052
- Blood Res.
- 2019 Mar;54(1):23-30.
- doi: 10.5045/br.2019.54.1.23
BACKGROUND: Hematopoietic stem cell transplantation (HSCT) patients need parenteral nutrition because of nausea, vomiting, and mucositis caused by conditioning regimens. The demand for glutamine increases during the HSCT period. We... -
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- Biphenotypic acute leukemia or acute leukemia of ambiguous lineage in childhood: clinical characteristics and outcome
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Lee HG, Baek HJ, Kim HS, Park SM, Hwang TJ, Kook H
- KMID: 2451058
- Blood Res.
- 2019 Mar;54(1):63-73.
- doi: 10.5045/br.2019.54.1.63
BACKGROUND: Acute leukemia (AL), not clearly assigned to myeloid, B-lymphoid, or T-lymphoid lineage, is classified as either biphenotypic acute leukemia (BAL) based on the European Group for Immunological Classification of... -
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- Outcome and prognostic factors of children with Philadelphia chromosome-positive acute lymphoblastic leukemia treated with imatinib followed by allogeneic hematopoietic cell transplantation in first remission
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Shin J, Lee NY, Kim S, Lee JW, Jang PS, Chung NG, Cho B
- KMID: 2451055
- Blood Res.
- 2019 Mar;54(1):45-51.
- doi: 10.5045/br.2019.54.1.45
BACKGROUND: Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) is a subset of ALL with poor prognosis. Here, we analyzed the outcomes and prognostic factors of children with Ph+ ALL who... -
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