Archives of hematology and blood diseases最新文献

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The Role of Magnesium as Immunomodulator and Mediator between Immune and Colon Cancer Cells 镁在免疫和结肠癌细胞间的免疫调节剂和中介作用
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0202002
C. Leibovitch, Esther Ganelin Cohen, M. Djaldetti, H. Bessler
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引用次数: 1
Day-Per-Day Maintenance and Six Sigma of the Landwind LW D3600 Hematological Analyzer: Clinical Aspects and Quality Verification 陆风LW D3600血液分析仪的日常维护和六西格玛:临床方面和质量验证
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0201004
Jeel Moya-Salazar
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引用次数: 1
Heavy Metal Bioaccumulation, Urinary Microalbumin and Some Haematological Variables among Artisans in Jos Metropolis 乔斯市工匠重金属生物积累、尿微量白蛋白及一些血液学变量
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0201005
Bot Yakubu S, Nwanjo Harrison U, Nwosu Dennis C, Lugos Moses D
{"title":"Heavy Metal Bioaccumulation, Urinary Microalbumin and Some Haematological Variables among Artisans in Jos Metropolis","authors":"Bot Yakubu S, Nwanjo Harrison U, Nwosu Dennis C, Lugos Moses D","doi":"10.22259/2639-3581.0201005","DOIUrl":"https://doi.org/10.22259/2639-3581.0201005","url":null,"abstract":"","PeriodicalId":93414,"journal":{"name":"Archives of hematology and blood diseases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68287756","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Maternal Genetics, Health and Hematological Profile of Pregnant Women in Madhya Pradesh, India 印度中央邦孕妇的母体遗传、健康和血液学概况
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0202003
R. Balgir
{"title":"Maternal Genetics, Health and Hematological Profile of Pregnant Women in Madhya Pradesh, India","authors":"R. Balgir","doi":"10.22259/2639-3581.0202003","DOIUrl":"https://doi.org/10.22259/2639-3581.0202003","url":null,"abstract":"","PeriodicalId":93414,"journal":{"name":"Archives of hematology and blood diseases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68287857","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary Large B Cell Lymphoma in the Tibia of an Old Individual Relapsing at an Uncommon Location 老年人胫骨原发性大B细胞淋巴瘤在不常见部位复发
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0202001
Meir Djaldetti M.D
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引用次数: 0
Amino Acids in the Diagnosis and Treatment of Liver Damage (Review) 氨基酸在肝损伤诊断和治疗中的应用(综述)
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0202005
I. I. Nefyodov, A. J. Karakosh, M. A. Alufaini, P. Karavay, N. Karavay
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引用次数: 0
Improved Treatment Related Mortality in Patients with Primary Systemic Amyloidosis (AL Amyloidosis) undergoing Autologous Hematopoietic Stem Cell Transplant (aHSCT). 自体造血干细胞移植(aHSCT)改善原发性系统性淀粉样变性(AL淀粉样变性)患者的治疗相关死亡率
Akshata Pandit, Lai Wei, Luis Bustamante, Patrick Elder, William B S Falk, Megan Sell, Ashley Rosko, Don M Benson, Steven M Devine, Craig C Hofmeister, Yvonne A Efebera
{"title":"Improved Treatment Related Mortality in Patients with Primary Systemic Amyloidosis (AL Amyloidosis) undergoing Autologous Hematopoietic Stem Cell Transplant (aHSCT).","authors":"Akshata Pandit,&nbsp;Lai Wei,&nbsp;Luis Bustamante,&nbsp;Patrick Elder,&nbsp;William B S Falk,&nbsp;Megan Sell,&nbsp;Ashley Rosko,&nbsp;Don M Benson,&nbsp;Steven M Devine,&nbsp;Craig C Hofmeister,&nbsp;Yvonne A Efebera","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>To date, there is no standard of care for patients with newly diagnosed Primary (AL) amyloidosis. Autologous hematopoietic stem cell transplant (aHSCT) is a reasonable option, but has been limited in its use due to increase in treatment-related mortality (TRM). We retrospectively analyzed the outcomes of 42 newly diagnosed consecutive AL amyloidosis patients transplanted at our center. The median age at aHSCT was 57.5 (range 26-71). Twenty one (50%) had involvement of at least two organs and 40 (97%) patients had cardiac stage I or II. Patients received high dose Melphalan 140(n=4) or 200(n=38) mg/m<sup>2</sup>. Median times to neutrophil and platelet engraftments were 12 and 18 days, respectively. Three months hematologic response were complete response in 21 patients (50%), very good partial response in 4 (10%), partial response in 5 (12%) and Minimal/Stable disease in 6(15%). The respective 1, 3, and 5 year progression-free survival were 79%, 67% and 57%, and overall survival from Transplant 81%, 73% and 66%. Day 100 and 1 year TRM were 4.8% and 7.1% respectively. Our results show that aHSCT is a safe and reasonable option for patients with AL amyloidosis. Day 100 and 1 year TRM compares favorably to multiple myeloma patients undergoing aHSCT.</p>","PeriodicalId":93414,"journal":{"name":"Archives of hematology and blood diseases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734359/pdf/nihms-1573589.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39804557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Is Screening of Blood Donors for G6PD Deficiency and Hemoglobinopathies a Necessity for Transfusion Medicine in India? 对献血者进行G6PD缺乏症和血红蛋白病筛查是印度输血医学的必要条件吗?
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0202004
R. Balgir
{"title":"Is Screening of Blood Donors for G6PD Deficiency and Hemoglobinopathies a Necessity for Transfusion Medicine in India?","authors":"R. Balgir","doi":"10.22259/2639-3581.0202004","DOIUrl":"https://doi.org/10.22259/2639-3581.0202004","url":null,"abstract":"","PeriodicalId":93414,"journal":{"name":"Archives of hematology and blood diseases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68287873","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lp-PLA2 Activity During Iron Depletion Treatment in Primary IO Patients 原发性IO患者缺铁治疗期间Lp-PLA2活性
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0201002
Tetzlaff Walter F, Martin Maximiliano E, Botta Eliana E, Saez Maria S, Ferraro Florencia M, Boero Laura E, Sorroche Patricia B, Arbelbide Jorge, Brites Fernando, Merono Tomas
{"title":"Lp-PLA2 Activity During Iron Depletion Treatment in Primary IO Patients","authors":"Tetzlaff Walter F, Martin Maximiliano E, Botta Eliana E, Saez Maria S, Ferraro Florencia M, Boero Laura E, Sorroche Patricia B, Arbelbide Jorge, Brites Fernando, Merono Tomas","doi":"10.22259/2639-3581.0201002","DOIUrl":"https://doi.org/10.22259/2639-3581.0201002","url":null,"abstract":"","PeriodicalId":93414,"journal":{"name":"Archives of hematology and blood diseases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68287590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improved Treatment Related Mortality in Patients with Primary Systemic Amyloidosis (AL Amyloidosis) undergoing Autologous Hematopoietic Stem Cell Transplant (aHSCT). 自体造血干细胞移植(aHSCT)改善原发性系统性淀粉样变性(AL淀粉样变性)患者的治疗相关死亡率
Archives of hematology and blood diseases Pub Date : 2019-01-01 DOI: 10.22259/2639-3581.0201003
A. Pandit, Lai Wei, Luis Bustamante, P. Elder, W. Falk, M. Sell, A. Rosko, D. Benson, S. Devine, C. Hofmeister, Y. Efebera
{"title":"Improved Treatment Related Mortality in Patients with Primary Systemic Amyloidosis (AL Amyloidosis) undergoing Autologous Hematopoietic Stem Cell Transplant (aHSCT).","authors":"A. Pandit, Lai Wei, Luis Bustamante, P. Elder, W. Falk, M. Sell, A. Rosko, D. Benson, S. Devine, C. Hofmeister, Y. Efebera","doi":"10.22259/2639-3581.0201003","DOIUrl":"https://doi.org/10.22259/2639-3581.0201003","url":null,"abstract":"To date, there is no standard of care for patients with newly diagnosed Primary (AL) amyloidosis. Autologous hematopoietic stem cell transplant (aHSCT) is a reasonable option, but has been limited in its use due to increase in treatment-related mortality (TRM). We retrospectively analyzed the outcomes of 42 newly diagnosed consecutive AL amyloidosis patients transplanted at our center. The median age at aHSCT was 57.5 (range 26-71). Twenty one (50%) had involvement of at least two organs and 40 (97%) patients had cardiac stage I or II. Patients received high dose Melphalan 140(n=4) or 200(n=38) mg/m2. Median times to neutrophil and platelet engraftments were 12 and 18 days, respectively. Three months hematologic response were complete response in 21 patients (50%), very good partial response in 4 (10%), partial response in 5 (12%) and Minimal/Stable disease in 6(15%). The respective 1, 3, and 5 year progression-free survival were 79%, 67% and 57%, and overall survival from Transplant 81%, 73% and 66%. Day 100 and 1 year TRM were 4.8% and 7.1% respectively. Our results show that aHSCT is a safe and reasonable option for patients with AL amyloidosis. Day 100 and 1 year TRM compares favorably to multiple myeloma patients undergoing aHSCT.","PeriodicalId":93414,"journal":{"name":"Archives of hematology and blood diseases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68287604","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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