Diagnosis of hereditary spherocytosis in newborn infants
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference21 articles.
1. Les manifestations néonatales de la maladie de Minkowski-Chauffard;Bernheim;Ann Pediatr (Paris),1960
2. Hemolytic disease in the neonatal period and early infancy;Erlandson;J Pediatr,1959
3. Autohemolysis of cord blood in congenital spherocytosis and ABO incompatibility;Kostinas;J Pediatr,1967
4. Hereditary spherocytosis in the neonatal period;Shapiro;J Pediatr,1957
5. Hemolytic disease of the newborn due to anti-A;Crawford;Blood,1953
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1. Red cell disorders: anaemia, jaundice, polycythaemia and cyanosis;Neonatal Haematology;2022-06-10
2. Difficulty in Diagnosis of Hereditary Spherocytosis in the Neonate;Pediatrics;2021-09-01
3. Neonatal anemia: Revisiting the enigmatic pyknocyte;American Journal of Hematology;2017-05-26
4. Developmental Erythropoiesis;Fetal and Neonatal Physiology;2017
5. Early postnatal diagnosis of hereditary spherocytosis by combining light microscopy, acidified glycerol lysis test and eosin-5′-maleimide binding assay;Annals of Hematology;2015-09-04
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