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.
9. [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]
10. Abnormalities of the erythrocyte membrane. Gallagher PG Pediatr Clin North Am; 2013 Dec; 60(6):1349-62. PubMed ID: 24237975 [TBL] [Abstract][Full Text] [Related]
11. Grandeur in the red blood cell. Young LE Hosp Pract (Off Ed); 1984 Oct; 19(10):16-7, 20, 22. PubMed ID: 6434556 [No Abstract] [Full Text] [Related]
12. Hemolytic anemias associated with deficient or dysfunctional spectrin. Lux SE; Pease B; Tomaselli MB; John KM; Bernstein SE Prog Clin Biol Res; 1979; 30():463-9. PubMed ID: 531037 [TBL] [Abstract][Full Text] [Related]
13. [Hereditary diseases of the human erythrocyte membrane skeleton (author's transl)]. Boivin P Nouv Presse Med; 1982 Jul; 11(31):2347-51. PubMed ID: 7111000 [TBL] [Abstract][Full Text] [Related]
14. The topology of red cell membrane lipids in hereditary spherocytosis. Zail SS; van den Hoek AK S Afr J Med Sci; 1975; 40(3):67-72. PubMed ID: 1198205 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Disorders of red cell membrane. An X; Mohandas N Br J Haematol; 2008 May; 141(3):367-75. PubMed ID: 18341630 [TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton. Gallagher PG; Tse WT; Forget BG Semin Perinatol; 1990 Oct; 14(5):351-67. PubMed ID: 2287951 [No Abstract] [Full Text] [Related]
19. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias? Giorgi M; Cianci CD; Gallagher PG; Morrow JS Exp Mol Pathol; 2001 Jun; 70(3):215-30. PubMed ID: 11418000 [TBL] [Abstract][Full Text] [Related]
20. [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; 203(4):284-95. PubMed ID: 1942935 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]