HEREDITARY METHEMOGLOBINEMIC CYANOSIS IN A MAN WITH ATRIAL SEPTAL DEFECT

Overview

Journal Can Med Assoc J

Specialty General Medicine

Date 1965 Feb 27

PMID 14259339

Citations 1

Authors

J C SPEARS

J L NAIMAN

J R Evans

J H CROOKSTON

Affiliations

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Citing Articles

[Familial deficiency of NADH-dependent methemoglobin-reductase associated with glycerin-1-phosphate-dehydrogenase activity in the erythrocytes].

Kubler W, Kuhn H, Mertens H, Seipel L Klin Wochenschr. 1971; 49(23):1294-8.

PMID: 5135950 DOI: 10.1007/BF01733086.

References

HECK W, Wolf H . [Congenital cardiac defect with cyanosis caused by pathological blood pigment (hemoglobin M)]. Ann Paediatr. 1958; 190(3):135-46. View

Bono G, GAMALERO P . [Further data on the study of constitutional methemoglobinemic cyanosis:2 case reports]. Minerva Pediatr. 1958; 10(41):1076-82. View

ZINKHAM W . An in-vitro abnormality of glutathione metabolism in erythrocytes from normal newborns: mechanism and clinical significance. Pediatrics. 1959; 23(1 Pt 1):18-32. View

HARLEY J, Mauer A . Studies on the formation of Heinz bodies. I. Methemoglobin production and oxyhemoglobin destruction. Blood. 1960; 16:1722-35. View

GERALD P, Efron M . Chemical studies of several varieties of Hb M. Proc Natl Acad Sci U S A. 1961; 47:1758-67. PMC: 223207. DOI: 10.1073/pnas.47.11.1758. View