[Survival of the erythrocytes of patients with congenital methemoglobinemia transfused into normal subjects]. 1960

G MISSALE, and G COCCONI, and S BURBI

UI MeSH Term Description Entries
D008708 Methemoglobinemia The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed) Methemoglobinemias
D004912 Erythrocytes Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. Blood Cells, Red,Blood Corpuscles, Red,Red Blood Cells,Red Blood Corpuscles,Blood Cell, Red,Blood Corpuscle, Red,Erythrocyte,Red Blood Cell,Red Blood Corpuscle
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

G MISSALE, and G COCCONI, and S BURBI
May 1949, Journal of clinical pathology,
G MISSALE, and G COCCONI, and S BURBI
May 1951, Journal of clinical pathology,
G MISSALE, and G COCCONI, and S BURBI
February 1976, The Journal of parasitology,
G MISSALE, and G COCCONI, and S BURBI
June 1952, Klinische Wochenschrift,
G MISSALE, and G COCCONI, and S BURBI
November 1967, Biochemical and biophysical research communications,
G MISSALE, and G COCCONI, and S BURBI
September 1955, Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete,
G MISSALE, and G COCCONI, and S BURBI
September 1965, American journal of veterinary research,
G MISSALE, and G COCCONI, and S BURBI
January 1947, Proceedings [of the] annual meeting. Central Society for Clinical Research (U.S.),
Copied contents to your clipboard!