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Journal Abstract Search
226 related items for PubMed ID: 2170705
21. [A case of hemolytic anemia with stomatocytosis]. Turpin F, Lortholary P, Lejeune F, Claer R. Nouv Rev Fr Hematol; 1971; 11(4):585-94. PubMed ID: 4257433 [No Abstract] [Full Text] [Related]
22. Dehydrated hereditary stomatocytosis is associated with neonatal hepatitis. Rees DC, Portmann B, Ball C, Mieli-Vergani G, Nicolaou A, Chetty MC, Stewart GW. Br J Haematol; 2004 Jul; 126(2):272-6. PubMed ID: 15238150 [Abstract] [Full Text] [Related]
23. Study of erythrocytes in a hereditary hemolytic syndrome (HHS): comparison with erythrocytes in lecithin:cholesterol acyltransferase (LCAT) deficiency. Godin DV, Gray GR, Frohlich J. Scand J Haematol; 1980 Feb; 24(2):122-30. PubMed ID: 6246569 [Abstract] [Full Text] [Related]
24. Correction of the permeability defect in hereditary stomatocytosis by dimethyl adipimidate. Mentzer WC, Lubin BH, Emmons S. N Engl J Med; 1976 May 27; 294(22):1200-4. PubMed ID: 1264135 [Abstract] [Full Text] [Related]
25. A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosis. Marcello AP, Vercellati C, Fermo E, Bianchi P, Zaninoni A, Barcellini W, Zanella A. Blood Cells Mol Dis; 2008 May 27; 41(3):261-2. PubMed ID: 18708292 [No Abstract] [Full Text] [Related]
26. [Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia]. Schröter W, Eber SW. Monatsschr Kinderheilkd; 1989 Jul 27; 137(7):368-79. PubMed ID: 2677683 [Abstract] [Full Text] [Related]
27. [Five cases of hereditary high red cell membrane phosphatidylcholine hemolytic anemia in three families]. Wakita M, Matsui T, Tsuzuki M, Nomura T, Miyazaki H, Kojima H, Maruyama F, Okamoto M, Ino T, Ezaki K, Sugihara T, Kanzaki A, Yawata Y, Hirano M. Rinsho Ketsueki; 1996 Mar 27; 37(3):265-70. PubMed ID: 8727354 [Abstract] [Full Text] [Related]
28. Hereditary stomatocytosis: association of low 2,3-diphosphoglycerate with increased cation pumping by the red cell. Wiley JS, Cooper RA, Adachi K, Asakura T. Br J Haematol; 1979 Jan 27; 41(1):133-41. PubMed ID: 420735 [Abstract] [Full Text] [Related]
29. [Congenital stomatocytosis associated with decreased sodium content in red cells]. Masuda M, Kokago H, Oshimi K, Mizoguchi H, Hashimoto M, Kanzaki A, Yawata Y. Rinsho Ketsueki; 1987 Jun 27; 28(6):872-5. PubMed ID: 3669325 [No Abstract] [Full Text] [Related]
30. [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 27; 25(1):7-16. PubMed ID: 6835836 [Abstract] [Full Text] [Related]
31. Hereditary dehydrated and overhydrated stomatocytosis: recent advances. Delaunay J, Stewart G, Iolascon A. Curr Opin Hematol; 1999 Mar 27; 6(2):110-4. PubMed ID: 10088641 [Abstract] [Full Text] [Related]
32. The Japanese family of congenital hemolytic anemia with high red cell membrane phosphatidyl choline and increased sodium transport. Yawata Y, Takemoto Y, Yoshimoto M, Miyashima K, Koresawa S, Mori M, Miwa T, Murai Y. Nihon Ketsueki Gakkai Zasshi; 1982 Jul 27; 45(4):672-81. PubMed ID: 7136463 [No Abstract] [Full Text] [Related]
33. Osmotic fragility and Na+-K+ ATPase activity of erythrocytes of HIV/AIDS patients. Ebuehi OA, Balogun MO, Audu RA, Idigbe EO. Saudi Med J; 2003 Dec 27; 24(12):1412-4. PubMed ID: 14710299 [No Abstract] [Full Text] [Related]
34. [Na and K cation levels and exchange across the membrane of the erythrocyte. II. Results obtained in the erythrocytes of 20 patients with congenital hemolytic anemia]. Bernard JF, Afifi F, Boivin P. Pathol Biol (Paris); 1974 Jan 27; 22(1):51-60. PubMed ID: 4592413 [No Abstract] [Full Text] [Related]
35. Beneficial influence of dietary curcumin, capsaicin and garlic on erythrocyte integrity in high-fat fed rats. Kempaiah RK, Srinivasan K. J Nutr Biochem; 2006 Jul 27; 17(7):471-8. PubMed ID: 16263255 [Abstract] [Full Text] [Related]
36. Antiphospholipid antibodies in a family with dehydrated hereditary stomatocytosis. Martinaud C, Gisserot O, Graffin B, Gaillard T, Brisou P, Cynober T, de Jaureguiberry JP, Delaunay J, Aguilon P. Thromb Res; 2008 Jul 27; 122(4):572-5. PubMed ID: 18377960 [No Abstract] [Full Text] [Related]
37. The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations. Delaunay J. Semin Hematol; 2004 Apr 27; 41(2):165-72. PubMed ID: 15071792 [Abstract] [Full Text] [Related]
38. Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells. Rivera A, Vandorpe DH, Shmukler BE, Andolfo I, Iolascon A, Archer NM, Shabani E, Auerbach M, Hamerschlak N, Morton J, Wohlgemuth JG, Brugnara C, Snyder LM, Alper SL. Am J Physiol Cell Physiol; 2019 Aug 01; 317(2):C287-C302. PubMed ID: 31091145 [Abstract] [Full Text] [Related]
39. Hereditary stomatocytosis: membrane and metabolism studies. Mentzer WC, Smith WB, Goldstone J, Shohet SB. Blood; 1975 Nov 01; 46(5):659-69. PubMed ID: 1174702 [Abstract] [Full Text] [Related]
40. Advances in understanding the pathogenesis of red cell membrane disorders. Iolascon A, Andolfo I, Russo R. Br J Haematol; 2019 Oct 01; 187(1):13-24. PubMed ID: 31364155 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]