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Journal Abstract Search
360 related items for PubMed ID: 2677683
1. [Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia]. Schröter W, Eber SW. Monatsschr Kinderheilkd; 1989 Jul; 137(7):368-79. PubMed ID: 2677683 [Abstract] [Full Text] [Related]
2. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]. Eber SW. Klin Padiatr; 1991 Jul; 203(4):284-95. PubMed ID: 1942935 [Abstract] [Full Text] [Related]
3. Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies. Yawata Y, Kanzaki A, Inoue T, Ata K, Wada H, Okamoto N, Higo I, Yawata A, Sugihara T, Yamada O. Int J Hematol; 1994 Jul; 60(1):23-38. PubMed ID: 7919236 [Abstract] [Full Text] [Related]
8. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis. Agre P, Asimos A, Casella JF, McMillan C. N Engl J Med; 1986 Dec 18; 315(25):1579-83. PubMed ID: 3785322 [Abstract] [Full Text] [Related]
10. [Congenital hemolytic anemias]. Schwarzmeier JD, Moser K, Pohl A. Acta Med Austriaca; 1979 Dec 18; 6(5):169-74. PubMed ID: 555211 [Abstract] [Full Text] [Related]
11. [Molecular pathology of the erythrocyte membrane]. Delaunay J. Rev Prat; 1993 Jun 01; 43(11):1392-6. PubMed ID: 8235389 [Abstract] [Full Text] [Related]
12. [Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]. Dhermy D, Féo C, Garbarz M, Bournier O, Dommergues JP, Garcia J, Boivin P, Tchernia G. Nouv Rev Fr Hematol (1978); 1983 Jun 01; 25(1):7-16. PubMed ID: 6835836 [Abstract] [Full Text] [Related]
17. Erythrocyte membrane defects in hemolytic anemias found through derivative thermal analysis of electric impedance. Ivanov IT, Tolekova A, Chakaarova P. J Biochem Biophys Methods; 2007 Jun 10; 70(4):641-8. PubMed ID: 17395266 [Abstract] [Full Text] [Related]
18. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Mariani M, Barcellini W, Vercellati C, Marcello AP, Fermo E, Pedotti P, Boschetti C, Zanella A. Haematologica; 2008 Sep 10; 93(9):1310-7. PubMed ID: 18641031 [Abstract] [Full Text] [Related]