Spherocytosis, Hereditary
This graph shows the total number of publications written about "Spherocytosis, Hereditary" by people in the URMC Research Network by year, and whether "Spherocytosis, Hereditary" was a major or minor topic of these publication.
Below are the most recent publications written about "Spherocytosis, Hereditary" by people in Profiles.
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Gallagher PG, Steiner LA, Liem RI, Owen AN, Cline AP, Seidel NE, Garrett LJ, Bodine DM. Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis. J Clin Invest. 2010 Dec 1; 120(12):4453-65.
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Segel GB, Hirsh MG, Feig SA. Managing anemia in pediatric office practice: Part 1. Pediatr Rev. 2002 Mar; 23(3):75-84.
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Korones D, Pearson HA. Normal erythrocyte osmotic fragility in hereditary spherocytosis. J Pediatr. 1989 Feb; 114(2):264-6.
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Waugh RE, Agre P. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis. J Clin Invest. 1988 Jan; 81(1):133-41.
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Waugh RE. Effects of inherited membrane abnormalities on the viscoelastic properties of erythrocyte membrane. Biophys J. 1987 Mar; 51(3):363-9.
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Waugh RE. Effects of abnormal cytoskeletal structure on erythrocyte membrane mechanical properties. Cell Motil. 1983; 3(5-6):609-22.
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Waugh RE, La Celle PL. Abnormalities in the membrane material properties of hereditary spherocytes. J Biomech Eng. 1980 Aug; 102(3):240.
