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Blood Research

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https://www.readbyqxmd.com/read/28698857/ultrasound-guided-sternal-bone-marrow-aspiration
#1
Yusuke Asakura, Maho Kinoshita, Yusuke Kasuya, Shiori Sakuma, Makoto Ozaki
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698856/the-first-case-of-paroxysmal-nocturnal-hemoglobinuria-and-budd-chiari-syndrome-treated-with-complement-inhibitor-eculizumab-in-korea
#2
Hyerim Kim, In-Suk Kim, Su-Hee Cho, Hyun Ji Lee, Chulhun L Chang, Ki Tae Yoon
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698855/the-imbalance-of-procoagulant-and-anticoagulant-factors-in-patients-with-chronic-liver-diseases-in-north-india
#3
Priyanka Saxena, Chhagan Bihari, Roshni Mirza, Ajeet Singh Bhadoria, Shiv K Sarin
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698854/utility-of-an-immunoglobulin-gene-rearrangement-assay-based-on-multiplex-pcr-in-detecting-bone-marrow-involvement-in-b-cell-non-hodgkin-lymphoma
#4
Dong Jin Park, Hyoun Chan Cho, Jung Hye Kwon, Ji-Young Park
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698853/hairy-cell-leukemia-a-case-report-of-atypical-presentation-without-splenomegaly
#5
Mona Alfaraj, Hussain Alsaeed
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698852/acute-megakaryoblastic-blast-crisis-as-a-presentation-manifestation-of-chronic-myelogenous-leukemia
#6
Jenna B Bhattacharya, Richa Gupta, Amit Samadhiya
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698851/impact-of-labile-plasma-iron-and-iron-chelation-on-the-viability-of-cultured-mononuclear-cells-from-patients-undergoing-autologous-hematopoietic-stem-cell-transplantation
#7
Flávio Augusto Naoum, Breno Pannia Espósito, Idiberto José Zotarelli Filho
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698850/comparison-of-the-characteristics-of-two-hemoglobin-variants-hb-d-iran-and-hb-e-eluting-in-the-hb-a2-window
#8
Jasmita Dass, Aastha Gupta, Suchi Mittal, Amrita Saraf, Sabina Langer, Manorama Bhargava
BACKGROUND: Cation exchange-high performance liquid chromatography (CE-HPLC) is most commonly used to evaluate hemoglobin (Hb) variants, which elute in the Hb A2 window. This study aimed to assess prevalence of an uncommon Hb variant, Hb D-Iran, and compare its red cell parameters and peak characteristics with those of Hb E that commonly elutes in the Hb A2 window. METHODS: Generally, we assess abnormal Hb using CE-HPLC as the primary technique along with alkaline and acid electrophoresis...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698849/clinical-characteristics-treatment-and-outcome-of-primary-rectal-lymphoma-a-single-center-experience-of-16-patients
#9
Jae Ho Jeong, Shin Kim, Jeong Eun Kim, Dok Hyun Yoon, Sang-Wook Lee, Jooryung Huh, Cheolwon Suh
BACKGROUND: The rectum is a relatively uncommon site for lymphoma compared with other gastrointestinal sites; no consensus regarding management of primary rectal lymphoma (PRL) has been formed due to its limited frequency. We aimed to investigate clinical characteristics and treatment outcomes in patients with PRL in a single center patient cohort. METHODS: We retrospectively analyzed the results of 16 consecutive patients with PRL, identified and treated at the Asan Medical Center, Seoul, Korea between January 1993 and December 2014...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698848/treatment-and-response-of-autoimmune-cytopenia-occurring-after-allogeneic-hematopoietic-cell-transplantation-in-children
#10
Seok Hwang-Bo, Seong-Koo Kim, Jae Wook Lee, Pil-Sang Jang, Nack-Gyun Chung, Dae-Chul Jeong, Bin Cho, Hack-Ki Kim
BACKGROUND: Autoimmune cytopenia (AIC) is a rare complication of allogeneic hematopoietic cell transplantation (HCT). In this study, we reviewed the diagnosis, treatment and response to therapy for pediatric patients with post-HCT AIC at our institution. METHODS: Of the 292 allogeneic HCTs performed from January, 2011 to December, 2015 at the Department of Pediatrics, The Catholic University of Korea, seven were complicated by post-HCT AIC, resulting in an incidence of 2...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698847/evaluation-of-a-new-flow-cytometry-based-method-for-detection-of-bcr-abl1-fusion-protein-in-chronic-myeloid-leukemia
#11
Swati Dasgupta, Ujjal K Ray, Arpita Ghosh Mitra, Deboshree M Bhattacharyya, Ashis Mukhopadhyay, Priyabrata Das, Sudeshna Gangopadhyay, Sudip Roy, Soma Mukhopadhyay
BACKGROUND: Philadelphia chromosome, a hallmark of chronic myeloid leukemia (CML), plays a key role in disease pathogenesis. It reflects a balanced reciprocal translocation between long arms of chromosomes 9 and 22 involving BCR and ABL1 genes, respectively. An accurate and reliable detection of BCR-ABL fusion gene is necessary for the diagnosis and monitoring of CML. Previously, many technologies, most of which are laborious and time consuming, have been developed to detect BCR-ABL chimeric gene or chromosome...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698846/evaluation-of-the-role-of-tax-hbz-and-htlv-1-proviral-load-on-the-survival-of-atll-patients
#12
Mohammad Mehdi Akbarin, Abbas Shirdel, Alireza Bari, Seyedeh Tahereh Mohaddes, Houshang Rafatpanah, Ehsan Ghayour Karimani, Kobra Etminani, Amin Golabpour, Reza Torshizi
BACKGROUND: Adult T-cell leukemia/lymphoma (ATLL) is an aggressive malignancy with very poor prognosis and short survival, caused by the human T-lymphotropic virus type-1 (HTLV-1). The HTLV-1 biomarkers trans-activator x (TAX) and HTLV-1 basic leucine zipper factor (HBZ) are main oncogenes and life-threatening elements. This study aimed to assess the role of the TAX and HBZ genes and HTLV-1 proviral load (PVL) in the survival of patients with ATLL. METHODS: Forty-three HTLV-1-infected individuals, including 18 asymptomatic carriers (AC) and 25 ATLL patients (ATLL), were evaluated between 2011 and 2015...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698845/intrachromosomal-amplification-of-chromosome-21-in-korean-pediatric-patients-with-b-cell-precursor-acute-lymphoblastic-leukemia-in-a-single-institution
#13
Mina Yang, Eun Sang Yi, Hee Jin Kim, Keon Hee Yoo, Hong Hoe Koo, Sun-Hee Kim
BACKGROUND: Intrachromosomal amplification of chromosome 21 (iAMP21), defined as the presence of three or more RUNX1 signals on one marker chromosome, is a distinct cytogenetic subgroup of childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL) that is known to have a poor prognosis when treated with standard therapy. The aim of this study was to evaluate the clinical characteristics of Korean children with iAMP21. METHODS: The cytogenetic data from BCP-ALL children were reviewed...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698844/dapsone-therapy-for-refractory-immune-thrombocytopenia-patients-a-case-series
#14
Ji Yun Lee, Jeong-Ok Lee, Joo Young Jung, Soo-Mee Bang
BACKGROUND: Dapsone has been recommended as a second-line immunosuppressive agent for patients with immune thrombocytopenia (ITP). METHODS: We retrospectively analyzed the efficacy and safety of dapsone therapy in patients with ITP. RESULTS: Nine ITP patients were treated with dapsone at a dose of 50-100 mg/day between May 2013 and March 2016. All patients were refractory to multiple previous treatments, with a median of 7 agents (range, 4-8), and 3 patients had undergone a previous splenectomy...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698843/diagnostic-approaches-for-inherited-hemolytic-anemia-in-the-genetic-era
#15
REVIEW
Yonggoo Kim, Joonhong Park, Myungshin Kim
Inherited hemolytic anemias (IHAs) are genetic diseases that present with anemia due to the increased destruction of circulating abnormal RBCs. The RBC abnormalities are classified into the three major disorders of membranopathies, hemoglobinopathies, and enzymopathies. Traditional diagnosis of IHA has been performed via a step-wise process combining clinical and laboratory findings. Nowadays, the etiology of IHA accounts for germline mutations of the responsible genes coding for the structural components of RBCs...
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698842/hemophagocytic-lymphohistiocytosis-secondary-to-histoplasmosis
#16
B K Karthik Bommanan, Shano Naseem, Neelam Varma
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698841/granulomatous-bone-marrow-involvement-of-hodgkin-lymphoma-nodular-sclerosis-type
#17
Se-Eun Koo, Chan-Jeoung Park
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698840/hematopoietic-stem-cell-mobilization-current-status-and-future-perspective
#18
Jin Seok Kim
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28698839/dapsone-therapy-for-immune-thrombocytopenic-purpura-old-but-still-unfamiliar
#19
EDITORIAL
Jaewoo Song
No abstract text is available yet for this article.
June 2017: Blood Research
https://www.readbyqxmd.com/read/28401110/the-first-case-report-of-a-patient-with-coexisting-hemophilia-b-and-down-syndrome
#20
Pulkit Rastogi, Narender Kumar, Jasmina Ahluwalia, Reena Das, Inusha Panigrahi
No abstract text is available yet for this article.
March 2017: Blood Research
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