Peripartum pulmonary embolism in a patient with concomitant hemoglobin newcastle, hemoglobin constant spring, and hereditary spherocytosis
Author:
Publisher
Wiley
Subject
Hematology
Reference5 articles.
1. Enhanced haemolysis with β-thalassaemia trait due to the unstable β chain variant, Hb Gunma, accompanied by hereditary elliptocytosis due to protein 4·1 deficiency in a Japanese family
2. Unstable Hb Newcastle [β92(F8)His→Pro], First Case Discovered in a Russian Patient
3. Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family
4. Pregnancy and hereditary spherocytosis
5. Postoperative Pulmonary Embolism in a Young Female Accompanying with Factor V Leiden Mutation and Hereditary Sypherocytosis
Cited by 3 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. A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next‐generation sequencing in a Chinese family;International Journal of Laboratory Hematology;2021-05-11
2. Hemoglobinopatía Newcastle: utilidad de la cromatografía y descripción del primer caso en España;Medicina Clínica;2008-04
3. Hyperbilirubinemia and cholelithiasis in Chinese patients with hemoglobin H disease;Annals of Hematology;2005-07-26
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