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22. [Intra-erythrocyte enzyme activities in normal and pathological states]. Vovan L; Orsini A Poumon Coeur; 1971; 27(7):673-81. PubMed ID: 5144943 [No Abstract] [Full Text] [Related]
23. The Stratton Lecture. Hemolytic anemia and inborn errors of metabolism. Valentine WN Blood; 1979 Sep; 54(3):549-59. PubMed ID: 572716 [No Abstract] [Full Text] [Related]
24. Frequency of enzyme deficiency variants in erythrocytes of newborn infants. Mohrenweiser HW Proc Natl Acad Sci U S A; 1981 Aug; 78(8):5046-50. PubMed ID: 6946452 [TBL] [Abstract][Full Text] [Related]
26. [Enzymes in medical genetics]. Lenz W Wien Klin Wochenschr; 1971 May; 83(20):348-53. PubMed ID: 4398925 [No Abstract] [Full Text] [Related]
27. A single amino acid substitution (Asp leads to Asn) in a phosphoglycerate kinase variant (PGK München) associated with enzyme deficiency. Fujii H; Krietsch WK; Yoshida A J Biol Chem; 1980 Jul; 255(13):6421-3. PubMed ID: 7391028 [TBL] [Abstract][Full Text] [Related]
28. Kinetic evidence for the interaction between rabbit muscle D-glyceraldehyde-3-phosphate dehydrogenase and 3-phosphoglycerate kinase. Sukhodolets MV; Muronetz VI; Nagradova NK Biochem Int; 1987 Aug; 15(2):373-9. PubMed ID: 3435530 [TBL] [Abstract][Full Text] [Related]
29. Crystalline 3-phospho-d-glycerate kinase from horse muscle. Johnson PE; Maister SG; Knowles JR Biochemistry; 1976 Jun; 15(13):2899-901. PubMed ID: 985698 [TBL] [Abstract][Full Text] [Related]
30. Congenital nonspherocytic hemolytic anemia associated with an unusual erythrocyte hexokinase abnormality. Necheles TF; Rai US; Cameron D J Lab Clin Med; 1970 Oct; 76(4):593-602. PubMed ID: 5458022 [No Abstract] [Full Text] [Related]
31. [Erythrocyte enzyme changes in hemophilia A]. Barretto OC; Pinheiro ED; Nonoyama K Rev Paul Med; 1985; 103(1):44-5. PubMed ID: 2994200 [No Abstract] [Full Text] [Related]
32. Deficiencies associated with Embden-Meyerhof pathway and other metabolic pathways. Valentine WN Semin Hematol; 1971 Oct; 8(4):348-66. PubMed ID: 4256808 [No Abstract] [Full Text] [Related]
34. The inherited defects of erythrocyte metabolism. Fornaini G; Bossu M Ital J Biochem; 1969; 18(4):185-326. PubMed ID: 4243574 [No Abstract] [Full Text] [Related]
35. [Erythrocytic enzyme defects in panmyelopathies]. Nowicki L; Behnken L; Biskamp K Verh Dtsch Ges Inn Med; 1971; 77():73-7. PubMed ID: 5155933 [No Abstract] [Full Text] [Related]
36. An evaluation of screening tests for erythrocyte enzyme deficiencies in a general hospital laboratory. Fox AR; Menkes AL J Am Osteopath Assoc; 1969 Nov; 69(3):255-61. PubMed ID: 5201294 [No Abstract] [Full Text] [Related]
37. Phosphoglycerate kinase A polymorphism in the wallaby Macropus parryi: activity of both X chromosomes in muscle. VandeBerg JL; Cooper DW; Sharman GB Nat New Biol; 1973 May; 243(123):47-8. PubMed ID: 17315363 [No Abstract] [Full Text] [Related]
38. [The activity of the enzyme galactokinase in the erythrocytes of healthy children and adults (author's transl)]. Sitzmann FC; Kaloud H; Teubl I; Müller HE Klin Padiatr; 1973 Nov; 185(6):444-8. PubMed ID: 4361008 [No Abstract] [Full Text] [Related]