These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
195 related items for PubMed ID: 408790
21. [Erythrocyte membrane protein abnormalities and membrane disease]. Yawata Y. Nihon Rinsho; 1979 Dec; 37(12):3885-99. PubMed ID: 395337 [No Abstract] [Full Text] [Related]
22. Proteolytic dissection of band 3 protein from human erythrocyte in congenital dyserythropoietic anemia type II. Sansone G, Scartezzini P, Baldi M, Forni GL, Veneziano G. Pathologica; 1981 Dec; 73(1026):623-8. PubMed ID: 7312435 [No Abstract] [Full Text] [Related]
23. [Case of congenital hemolytic anemia associated with high red cell membrane phosphatidyl choline and enhanced Na+-transport]. Karasawa M, Sawamura M, Okamoto K, Iwata N, Omine M, Maekawa T, Sugihara T, Yoshimoto M, Yawata Y. Rinsho Ketsueki; 1982 Nov; 23(11):1816-22. PubMed ID: 7166815 [No Abstract] [Full Text] [Related]
24. Erythrocyte lipids and vitamin E in type II congenital dyserythropoietic anemia. O'Regan S, Melhorn DK, Newman AJ, Graham RC. J Pediatr; 1974 Mar; 84(3):355-61. PubMed ID: 4811986 [No Abstract] [Full Text] [Related]
25. [Erythrocyte lipids in congenital sperocytosis]. van Gastel C. Folia Med Neerl; 1968 Mar; 11(3):94-5. PubMed ID: 5707014 [No Abstract] [Full Text] [Related]
26. Red cell membrane protein phosphorylation in hemolytic anemias and muscular dystrophies. Tsung PK, Palek J. Muscle Nerve; 1980 Mar; 3(1):55-69. PubMed ID: 6246419 [Abstract] [Full Text] [Related]
29. Hemolytic syndromes and red cell membrane abnormalities in liver disease. Cooper RA. Semin Hematol; 1980 Apr; 17(2):103-12. PubMed ID: 6990496 [No Abstract] [Full Text] [Related]
30. Red cell membrane proteins and lipids in spherocytosis. Johnsson R. Scand J Haematol; 1978 Apr; 20(4):341-50. PubMed ID: 653313 [No Abstract] [Full Text] [Related]
31. Clinical expression and laboratory detection of red blood cell membrane protein mutations. Palek J, Jarolim P. Semin Hematol; 1993 Oct; 30(4):249-83. PubMed ID: 8266114 [No Abstract] [Full Text] [Related]
32. Erythrocyte membrane vacuole formation in hereditary spherocytosis. Schrier SL, Ben-Bassat I, Bensch K, Seeger M, Junga I. Br J Haematol; 1974 Jan; 26(1):59-69. PubMed ID: 4368693 [No Abstract] [Full Text] [Related]
33. [A case of congenital hemolytic anemia with red cell membrane lipid abnormalities (increased phosphatidyl choline and free cholesterol) associated with enhanced sodium transport]. Haneda Y, Takemori H, Chiba Y, Yoshida Y, Saitoh Y, Sugihara T, Shimoda M, Yawata Y. Rinsho Ketsueki; 1984 Oct; 25(10):1692-8. PubMed ID: 6520943 [No Abstract] [Full Text] [Related]
34. Passive cation transport in hereditary xerocytosis. Fairbanks G, Dino JE, Snyder LM. Prog Clin Biol Res; 1984 Oct; 159():205-17. PubMed ID: 6473461 [No Abstract] [Full Text] [Related]