Hereditary spherocytosis in the neonatal period: Diagnosis, incidence, and treatment
- 31 March 1957
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 50 (3), 308-314
- https://doi.org/10.1016/s0022-3476(57)80028-6
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Icterus neonatorum gravis als Manifestation einer hereditären SphärocytoseEuropean Journal of Pediatrics, 1956
- Splenectomy in Infants and Children*Annals of Surgery, 1955
- Generalized cytomegalic inclusion disease: Report of a case and review of literatureThe Journal of Pediatrics, 1953
- Inclusion Disease in ChildhoodArchives of Disease in Childhood, 1951
- Acholuric Jaundice in a Newborn InfantArchives of Disease in Childhood, 1951
- CONGENITAL HEMOLYTIC JAUNDICE IN A NEGRO FAMILYThe Lancet Healthy Longevity, 1949
- A CLINICOPATHOLOGIC STUDY WITH PRESENTATION OF FIVE CASES AND REVIEW OF THE LITERATUREMedicine, 1946
- Haemolytic Disease and Congenital Syphilis in SiblingsBMJ, 1945
- Congenital haemolytic anaemia with normal fragility of the red blood cellsArchives of Disease in Childhood, 1938
- THE MEAN DIAMETER OF THE ERYTHROCYTES IN ACHOLURIC FAMILY JAUNDICE: AND THE EFFECTS OF SPLENECTOMYThe Lancet, 1934