A Novel Marker for Screening Paroxysmal Nocturnal Hemoglobinuria Using Routine Complete Blood Count and Cell Population Data
Author:
Affiliation:
1. Departments of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea
2. Departments of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea
Publisher
Annals of Laboratory Medicine
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://synapse.koreamed.org/pdf/10.3343/alm.2015.35.1.35
Reference27 articles.
1. Clinical signs and symptoms associated with increased risk for thrombosis in patients with paroxysmal nocturnal hemoglobinuria from a Korean Registry
2. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
3. The molecular basis of paroxysmal nocturnal hemoglobinuria
4. Paroxysmal Nocturnal Hemoglobinuria: An Historical Overview
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The effect of splenectomy on complement regulatory proteins in erythrocytes in β-thalassemia major;Archives of Medical Science;2019
2. Paroxysmal Nocturnal Hemoglobinuria: From Bench to Bed;Indian Journal of Hematology and Blood Transfusion;2016-02-12
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