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Journal Abstract Search
154 related items for PubMed ID: 647119
1. Marked reduction of spectrinin hereditary spherocytosis in the common house mouse. Greenquist AC, Shohet SB, Bernstein SE. Blood; 1978 Jun; 51(6):1149-55. PubMed ID: 647119 [Abstract] [Full Text] [Related]
2. Deficient red-cell spectrin in severe, recessively inherited spherocytosis. Agre P, Orringer EP, Bennett V. N Engl J Med; 1982 May 13; 306(19):1155-61. PubMed ID: 7070419 [No Abstract] [Full Text] [Related]
3. Spectrin and spherocytosis. Shohet SB. N Engl J Med; 1982 May 13; 306(19):1170-1. PubMed ID: 7070421 [No Abstract] [Full Text] [Related]
4. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil. Saad ST, Costa FF, Vicentim DL, Salles TS, Pranke PH. Br J Haematol; 1994 Oct 13; 88(2):295-9. PubMed ID: 7803273 [Abstract] [Full Text] [Related]
5. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis]. Ferrándiz F, Ródenas S, Villegas A. Sangre (Barc); 1993 Oct 13; 38(5):393-7. PubMed ID: 8140503 [Abstract] [Full Text] [Related]
6. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis. Waugh RE, Agre P. J Clin Invest; 1988 Jan 13; 81(1):133-41. PubMed ID: 3335631 [Abstract] [Full Text] [Related]
7. Lipid loss in spectrin deficient mouse erythrocytes. Shohet SB. Prog Clin Biol Res; 1979 Jan 13; 30():471-4. PubMed ID: 531038 [No Abstract] [Full Text] [Related]
8. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis. Coetzer TL, Lawler J, Liu SC, Prchal JT, Gualtieri RJ, Brain MC, Dacie JV, Palek J. N Engl J Med; 1988 Jan 28; 318(4):230-4. PubMed ID: 2961992 [No Abstract] [Full Text] [Related]
9. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins]. Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B. Rev Med Brux; 1998 Oct 28; 19(5 Pt 1):417-23. PubMed ID: 9844481 [Abstract] [Full Text] [Related]
10. A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency. Yaish HM, Christensen RD, Agarwal A. J Perinatol; 2013 May 28; 33(5):404-6. PubMed ID: 23624969 [Abstract] [Full Text] [Related]
11. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis. Liu SC, Derick LH, Agre P, Palek J. Blood; 1990 Jul 01; 76(1):198-205. PubMed ID: 2364170 [Abstract] [Full Text] [Related]
12. Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis. Chasis JA, Agre P, Mohandas N. J Clin Invest; 1988 Aug 01; 82(2):617-23. PubMed ID: 3403720 [Abstract] [Full Text] [Related]
13. Combined ankyrin and spectrin deficiency in hereditary spherocytosis. Pekrun A, Eber SW, Kuhlmey A, Schröter W. Ann Hematol; 1993 Aug 01; 67(2):89-93. PubMed ID: 8347735 [Abstract] [Full Text] [Related]
14. Phosphorylation in erythrocyte membranes from abnormally shaped cells. Greenquist AC, Shohet SB. Blood; 1976 Dec 01; 48(6):877-86. PubMed ID: 187264 [Abstract] [Full Text] [Related]
15. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases. Iolascon A, Miraglia del Giudice E, Camaschella C, Pinto L, Nobili B, Perrotta S, Cutillo S. Br J Haematol; 1991 Aug 01; 78(4):551-4. PubMed ID: 1832935 [Abstract] [Full Text] [Related]
16. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis. Goodman SR, Shiffer KA, Casoria LA, Eyster ME. Blood; 1982 Sep 01; 60(3):772-84. PubMed ID: 7104494 [Abstract] [Full Text] [Related]