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Journal Abstract Search
476 related items for PubMed ID: 10846232
1. [Hereditary diseases of erythrocyte membrane: from clinical aspects to underlying genetical and molecular mechanisms]. Bichis M, Huber AR. Ann Biol Clin (Paris); 2000; 58(3):277-89. PubMed ID: 10846232 [Abstract] [Full Text] [Related]
2. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Gallagher PG. Curr Hematol Rep; 2004 Mar; 3(2):85-91. PubMed ID: 14965483 [Abstract] [Full Text] [Related]
6. 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]
7. [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 Oct; 203(4):284-95. PubMed ID: 1942935 [Abstract] [Full Text] [Related]
8. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane]. Boivin P. J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209 [No Abstract] [Full Text] [Related]
9. [Red cell membrane disorders: historical perspectives from dawn to enlightenment (II)]. Yawata Y. Rinsho Ketsueki; 1999 Dec; 40(12):1223-35. PubMed ID: 10658475 [No Abstract] [Full Text] [Related]
10. [Hereditary diseases of the human erythrocyte membrane skeleton (author's transl)]. Boivin P. Nouv Presse Med; 1982 Jul 03; 11(31):2347-51. PubMed ID: 7111000 [Abstract] [Full Text] [Related]