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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1995 | 1 |
1996 | 4 |
2024 | 0 |
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5 results
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Page 1
Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
Am J Hematol. 1996 Feb;51(2):122-32. doi: 10.1002/(SICI)1096-8652(199602)51:2<122::AID-AJH5>3.0.CO;2-#.
Am J Hematol. 1996.
PMID: 8579052
Free article.
Review.
Five unknown mutations in the LR pyruvate kinase gene associated with severe hereditary nonspherocytic haemolytic anaemia in France.
Rouger H, Valentin C, Craescu CT, Galactéros F, Cohen-Solal M.
Rouger H, et al.
Br J Haematol. 1996 Mar;92(4):825-30. doi: 10.1046/j.1365-2141.1996.405941.x.
Br J Haematol. 1996.
PMID: 8616073
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Hematologically important mutations: red cell pyruvate kinase.
Baronciani L, Bianchi P, Zanella A.
Baronciani L, et al.
Blood Cells Mol Dis. 1996;22(1):85-9. doi: 10.1006/bcmd.1996.0012.
Blood Cells Mol Dis. 1996.
PMID: 8807089
No abstract available.
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Mutations in pyruvate kinase.
Beutler E, Baronciani L.
Beutler E, et al.
Hum Mutat. 1996;7(1):1-6. doi: 10.1002/(SICI)1098-1004(1996)7:1<1::AID-HUMU1>3.0.CO;2-H.
Hum Mutat. 1996.
PMID: 8664896
Review.
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Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia.
Baronciani L, Beutler E.
Baronciani L, et al.
J Clin Invest. 1995 Apr;95(4):1702-9. doi: 10.1172/JCI117846.
J Clin Invest. 1995.
PMID: 7706479
Free PMC article.
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