Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis-Reference-Cited by-同舟云学术

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Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis

Published:2017-10 Issue: Volume:16 Page:4-7
ISSN:2214-9112
Container-title:Case Reports in Women's Health
language:en
Short-container-title:Case Reports in Women's Health

Author:

Hannah Dawn M.,Tressler Terry B.,Taboada Claudia D.

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference8 articles.

1. Anemia and Pregnancy;Kilpatrick,2014

2. Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis;Yetgin;J. Perinatol.,2007

3. Deficiency of α-spectrin synthesis in burst forming units-erythroid in lethal hereditary spherocytosis;Whitfield;Blood,1991

4. Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene;Gallagher;J. Clin. Invest.,1995

Cited by 8 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. Homozygous SPTA1‐associated hereditary pyropoikilocytosis presenting as hydrops fetalis;Transfusion;2023-11-29

2. How do we perform intrauterine transfusions?;Transfusion;2023-10-27

3. Red cell disorders: anaemia, jaundice, polycythaemia and cyanosis;Neonatal Haematology;2022-06-10

4. Erythroblastosis Fetalis, Hydrops Fetalis, and Transplacental Hemorrhage;Benirschke's Pathology of the Human Placenta;2021-12-08

5. Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis;Medicine;2021-03-26

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