Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants-Reference-Cited by-同舟云学术

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Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants

Published:2014-11-06 Issue:5 Volume:35 Page:357-361
ISSN:0743-8346
Container-title:Journal of Perinatology
language:en
Short-container-title:J Perinatol

Author:

Christensen R D,Agarwal A M,Nussenzveig R H,Heikal N,Liew M A,Yaish H M

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Link

http://www.nature.com/articles/jp2014202.pdf

Reference33 articles.

1. Johnson L, Bhutani VK, Karp K, Sivieri EM, Shapiro SM . Clinical report from the pilot USA kernicterus registry (1992–2004). J Perinatol 2009; 29 (Suppl 1): S25–S45.

2. Christensen RD, Yaish HM, Nussenzveig RH, Reading NS, Agarwal AM, Eggert LD et al. Acute kernicterus in a neonate with O/B blood group incompatibility and a mutation in SLC4A1. Pediatrics 2013; 132 (2): e531–e534.

3. Gallagher PG . Abnormalities of the erythrocyte membrane. Pediatr Clin North Am 2013; 60 (6): 1349–1362.

4. Christensen RD, Henry E . Hereditary spherocytosis in neonates with hyperbilirubinemia. Pediatrics 2010; 125 (1): 120–125.

5. Sheffield MJ, Christensen RD . Evaluating neonatal hyperbilirubinemia in late preterm Hispanic twins led to the diagnosis of hereditary spherocytosis in them, and in their sibling and in their mother. J Perinatol 2011; 31 (9): 625–627.

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2. Neonatal Anemia;Principles of Neonatology;2024

3. Hereditary spherocytosis: review of cases and discussion of hematologic characteristics and updated diagnostic testing;Journal of Advanced Pediatrics and Child Health;2023-03-13

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

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