4.5 Review

Pathophysiology and management of inherited bone marrow failure syndromes

期刊

BLOOD REVIEWS
卷 24, 期 3, 页码 101-122

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.blre.2010.03.002

关键词

Aplastic anemia; Fanconi; Dyskeratosis congenita; Diamond-Blackfan anemia; Shwachman-Diamond syndrome; Inherited bone marrow failure syndromes

资金

  1. National Institutes of Health
  2. National Cancer Institute
  3. National Heart Lung and Blood Institute of the National Institutes of Health
  4. NATIONAL CANCER INSTITUTE [ZIACP010144] Funding Source: NIH RePORTER
  5. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL079582] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R24AI049393] Funding Source: NIH RePORTER

向作者/读者索取更多资源

The inherited marrow failure syndromes are a diverse set of genetic disorders characterized by hematopoietic aplasia and cancer predisposition. The clinical phenotypes are highly variable and much broader than previously recognized. The medical management of the inherited marrow failure syndromes differs from that of acquired aplastic anemia or malignancies arising in the general population. Diagnostic workup, molecular pathogenesis, and clinical treatment are reviewed. (C) 2010 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据