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We are the roots: Black Settlers and their Experiences of Discrimination on the Canadian Prairies by Dr. Jenna Bailey and Dr. David Este (review) 《我们是根源:加拿大大草原上的黑人定居者及其歧视经历》,作者:詹娜·贝利博士、大卫·埃斯特博士
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2019-08-01 DOI: 10.1093/OHR/OHZ014
Anna F. Kaplan
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引用次数: 1
Women of Rock Oral History Project. Sofia Smith Collection of Women's History, Smith College, Northampton, MA. 摇滚女性口述历史项目。索菲亚·史密斯收集妇女的历史,史密斯学院,北安普顿,马萨诸塞州。
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2019-03-01 DOI: 10.1093/ohr/ohy094
R. D. Gatchet
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引用次数: 0
Good Intentions: Grappling with Legacies of Conflict and Distrust Surrounding a Native American Oral History Project One Generation Later 良好的意图:在一代人之后,与围绕美国原住民口述历史项目的冲突和不信任的遗产作斗争
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2019-03-01 DOI: 10.1093/OHR/OHZ004
Melanie Shell-Weiss
Abstract This article focuses on an urban Native American oral history project the Grand Rapids Public Library carried out in Michigan between 1974 and 1978. Although the project itself lasted just four years, it cast a long shadow on West Michigan’s Native Americans and the city’s public library and public museum, and it shaped the lifework of several key individuals who went on to hold positions in federal agencies. Drawing heavily on information gleaned from preserved project records, this case study aims to deepen our understanding of community engagement and ethics and why community-based efforts launched with the best of intentions often fail. It also suggests considerations of sustaining value for kindred oral history efforts today, including not only the imperative of intercultural understanding but also the abiding need for researchers to think critically and intentionally about our own subjectivities, to demonstrate willingness not just to accept but to embrace conflict and to recognize our institutional obligations and the limits on our own decision-making powers.
摘要:本文主要关注1974年至1978年期间密歇根州大急流城公共图书馆开展的城市美洲原住民口述历史项目。虽然这个项目本身只持续了四年,但它给西密歇根州的印第安人、该市的公共图书馆和公共博物馆投下了长长的阴影,并影响了几位后来在联邦机构任职的关键人物的一生。本案例研究主要利用从保存完好的项目记录中收集到的信息,旨在加深我们对社区参与和道德的理解,以及为什么怀着最好的意图发起的以社区为基础的努力往往失败。它还建议考虑维持今天同类口述历史努力的价值,不仅包括跨文化理解的必要性,还包括研究人员对我们自己的主体性进行批判性和有意性思考的持久需求,表明不仅愿意接受而且愿意接受冲突,并认识到我们的制度义务和我们自己的决策权的限制。
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引用次数: 2
Faxed: The Rise and Fall of the Fax Machine by Jonathan Coopersmith (review) 传真:传真机的兴衰乔纳森·库珀史密斯(评论)
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2019-03-01 DOI: 10.1093/OHR/OHY091
David A. Olson
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引用次数: 0
Encounters with the People: Written and Oral Accounts of Nez Perce Life to 1858 eds. by Dennis Baird, Diane Mallickan, and William R. Swagerty (review) 《与人民的相遇:内兹珀斯人1858年生活的书面和口头记述》,作者:Dennis Baird、Diane Mallickan和William R.Swagerty(评论)
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2018-09-12 DOI: 10.5860/choice.195359
Debbiesiu L. Lee
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引用次数: 0
Updates in the systemic treatment of hepatocellular carcinoma 肝细胞癌全身治疗的最新进展
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2018-01-01 DOI: 10.17925/OHR.2018.14.2.76
E. Chen, C. Lopez, G. Vaccaro
Support: No funding was received for the publication of this article. Liver cancer has contributed to an annual 30,200 deaths in the US so far in 2018. An overwhelming majority is due to hepatocellular carcinoma (HCC) in the setting of advanced liver disease. While chronic hepatitis C and alcoholic liver disease traditionally have been the most common etiologies of cirrhosis in the US, the prevalence of non-alcoholic fatty liver disease is on the rise. Chronic hepatitis B is also important among patients who have emigrated from high-risk areas, such as east and southeast Asia, Africa, and South America.
支持:未收到用于发表本文的资金。到目前为止,2018年美国每年有30200人死于肝癌。绝大多数是由于肝细胞癌(HCC)在设置晚期肝病。在美国,慢性丙型肝炎和酒精性肝病一直是肝硬化最常见的病因,而非酒精性脂肪性肝病的患病率也在上升。慢性乙型肝炎在从高风险地区(如东亚和东南亚、非洲和南美洲)移民过来的患者中也很重要。
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引用次数: 1
Advances in Cancer Research and Translational Medicine 癌症研究与转化医学进展
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2018-01-01 DOI: 10.17925/OHR.2018.14.1.14
E. Mardis
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引用次数: 0
Pediatric Anaplastic Large Cell Lymphoma—A Review 儿童间变性大细胞淋巴瘤a综述
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2018-01-01 DOI: 10.17925/OHR.2018.14.1.21
Soumitra Tole, Laura Wheaton, S. Alexander
Anaplastic large cell lymphoma (ALCL) is the most common pediatric peripheral T-cell lymphoma, accounting for 10–15% of pediatric non-Hodgkin lymphoma. Patients with pediatric ALCL commonly present at an advanced stage of disease and, unlike adult ALCL, the majority of pediatric cases demonstrate overexpression of anaplastic lymphoma kinase (ALK). Despite a range of treatment strategies, event-free survival has remained stagnant at 65–75%. The role of novel targeted therapies such as ALK inhibitors and anti-CD30 antibody drug conjugates are actively being studied in both the newly diagnosed and relapse setting. This review article will cover the pathology, clinical presentation, and prognostic factors for pediatric ALCL, and will focus on a discussion of the therapeutic strategies for this disease.
间变性大细胞淋巴瘤(ALCL)是最常见的儿童外周t细胞淋巴瘤,占儿童非霍奇金淋巴瘤的10-15%。儿童ALCL患者通常出现在疾病的晚期,与成人ALCL不同,大多数儿童病例表现出间变性淋巴瘤激酶(ALK)的过度表达。尽管有一系列的治疗策略,无事件生存率仍然停滞在65-75%。新的靶向治疗如ALK抑制剂和抗cd30抗体药物偶联物在新诊断和复发环境中的作用正在积极研究中。这篇综述文章将涵盖儿科ALCL的病理、临床表现和预后因素,并将重点讨论这种疾病的治疗策略。
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引用次数: 4
Early Intervention in Multiple Myeloma—Exploring New Frontiers 多发性骨髓瘤的早期干预:探索新领域
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2018-01-01 DOI: 10.17925/OHR.2018.14.1.12
Shaji K. Kumar
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引用次数: 0
Bilateral Obliterative External Otitis in the Context of Chronic Iron Deficiency—Report of Two Cases 慢性缺铁伴双侧闭塞性外耳炎2例报告
IF 1.1 1区 历史学 Q1 HISTORY Pub Date : 2018-01-01 DOI: 10.17925/OHR.2018.14.1.42
M. Kmeid, J. Nehmé
Plummer-Vinson syndrome is a rare disorder consisting of a constellation of signs and symptoms related to a chronic iron deficiency state. Affected patients usually present with dysphagia secondary to esophageal hypomotility or web formation, oral manifestations such as glossitis, stomatitis, and cheilitis, and chronic sideropenic anemia. In this report, we present two cases where, in addition to these diseasedefining features, otologic symptoms were also found. Chronic stenosing external otitis with auditory canal web formation can represent, in this context, the manifestation of an underlying systemic cause and may be triggered by the same etiopathogenic factors that lead to esophageal dysfunction and web formation. As a result, a new perspective on the eponym of Plummer-Vinson disease is presented highlighting the wide and variable spectrum of head and neck manifestations of iron deficiency, a common but frequently overlooked medical condition.
普卢默-文森综合征是一种罕见的疾病,由一系列与慢性缺铁状态相关的体征和症状组成。受影响的患者通常表现为继发于食管低能或网状形成的吞咽困难,口腔表现如舌炎、口炎和口唇炎,以及慢性铁缺乏性贫血。在本报告中,我们报告了两个病例,除了这些疾病特征外,还发现了耳科症状。在这种情况下,慢性狭窄性外耳炎伴听道网形成可能是一种潜在的系统性原因的表现,并且可能由导致食道功能障碍和听道网形成的相同致病因素引发。因此,对普卢默-文森病的名字提出了一个新的观点,强调了铁缺乏的广泛和可变的头颈部表现,这是一种常见但经常被忽视的医学状况。
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引用次数: 2
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Oral History Review
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