Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1971 Feb;46(245):121–123. doi: 10.1136/adc.46.245.121

Favism in breast-fed infants.

S Taj-Eldin
PMCID: PMC1647560  PMID: 5555486

Full text

PDF
121

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CASPER J., SHULMAN J. Bilateral cortical necrosis of the kidneys in an infant with favism. Am J Clin Pathol. 1956 Jan;26(1):42–47. doi: 10.1093/ajcp/26.1.42. [DOI] [PubMed] [Google Scholar]
  2. EMANUEL B., SCHOENFELD A. Favism in a nursing infant. J Pediatr. 1961 Feb;58:263–266. doi: 10.1016/s0022-3476(61)80166-2. [DOI] [PubMed] [Google Scholar]
  3. GASSER C. Die hämolytische Frühgeburtenanämie mit spontaner Innènkörperbildung; ein neues Syndrom, beobachtet an 14 Fällen. Helv Paediatr Acta. 1953 Dec;8(6):491–529. [PubMed] [Google Scholar]
  4. HOLT J. M., SLADDEN R. A. FAVISM IN ENGLAND--TWO MORE CASES. Arch Dis Child. 1965 Jun;40:271–273. doi: 10.1136/adc.40.211.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. JOANNIDES C. C. Favism in Cyprus; analysis of 67 cases admitted to Nicosia General Hospital during the last 3 years. Cyprus Med J. 1952 Jan;5(3):795–799. [PubMed] [Google Scholar]
  6. LARKIN V. D. Favism; report of a case and brief review of the literature. J Pediatr. 1953 Apr;42(4):453–456. doi: 10.1016/s0022-3476(53)80460-9. [DOI] [PubMed] [Google Scholar]
  7. MARKS P. A., GROSS R. T. Erythrocyte glucose-6-phosphate dehydrogenase deficiency: evidence of differences between Negroes and Caucasians with respect to this genetically determined trait. J Clin Invest. 1959 Dec;38:2253–2262. doi: 10.1172/JCI104006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. SHAHIDI N. T., DIAMOND L. K. Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia. Pediatrics. 1959 Aug;24(2):245–253. [PubMed] [Google Scholar]
  9. TARLOV A. R., BREWER G. J., CARSON P. E., ALVING A. S. Primaquine sensitivity. Glucose-6-phosphate dehydrogenase deficiency: an inborn error of metabolism of medical and biological significance. Arch Intern Med. 1962 Feb;109:209–234. doi: 10.1001/archinte.1962.03620140081013. [DOI] [PubMed] [Google Scholar]
  10. ZINKHAM W. H. Peripheral blood and bilirubin values in normal full-term primaquine-sensitive Negro infants: effect of vitamin K. Pediatrics. 1963 Jun;31:983–995. [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES