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6. The effect of copper on red cell enzyme activities. Boulard M; Blume KG; Beutler E J Clin Invest; 1972 Feb; 51(2):459-61. PubMed ID: 4257805 [TBL] [Abstract][Full Text] [Related]
7. [Hemolytic anemias caused by genetic disorders in human red cells]. Benöhr HC Arztl Forsch; 1970 Jan; 24(1):19-29. PubMed ID: 4398687 [No Abstract] [Full Text] [Related]
8. Recent advances in knowledge of the hereditary haemolytic anaemias. Dacie JV Schweiz Med Wochenschr; 1968 Oct; 98(42):1624-9. PubMed ID: 4884035 [No Abstract] [Full Text] [Related]
9. [Trisomy-21 with deficiency of erythrocyte-phosphofructokinase]. Schwarzmeier J; Moser K; Zimprich H; Weiss I Z Kinderheilkd; 1970; 108(4):325-30. PubMed ID: 4252955 [No Abstract] [Full Text] [Related]
10. Study of the blood. N Engl J Med; 1969 Mar; 280(10):559-60. PubMed ID: 5764457 [No Abstract] [Full Text] [Related]
11. [Classification and screening of erythrocyte enzyme deficiencies]. Takagi K Nihon Rinsho; 1979 Jun; Suppl():2169-73. PubMed ID: 491101 [No Abstract] [Full Text] [Related]
12. Congenital hemolytic anemias and red cell enzyme deficiencies. Oski FA; Stockman JA Curr Probl Pediatr; 1973 Dec; 4(2):1-40. PubMed ID: 4272089 [No Abstract] [Full Text] [Related]
13. Molecular basis of red cell enzymopathies associated with hereditary nonspherocytic hemolytic anemia. Miwa S Haematologia (Budap); 1989; 22(4):215-31. PubMed ID: 2560452 [TBL] [Abstract][Full Text] [Related]
18. Red cell enzymopathies in the newborn. II. Inherited deficiencies of red cell enzymes. Travis SF Ann Clin Lab Sci; 1982; 12(3):163-77. PubMed ID: 6284015 [No Abstract] [Full Text] [Related]