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7. Ca2+ influx in normal and spherocytic red cells. Johnsson R; Saris NE Clin Chim Acta; 1988 May; 174(2):141-8. PubMed ID: 2454768 [TBL] [Abstract][Full Text] [Related]
8. Phosphorus-31 nuclear magnetic resonance studies of human red blood cells. Tehrani AY; Lam YF; Lin AK; Dosch SF; Ho C Blood Cells; 1982; 8(2):245-61. PubMed ID: 7159749 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. Regeneration of phosphorylated metabolites in stored erythrocytes in an open perfusion system: studies using 31P NMR spectroscopy. Chapman BE; Kuchel PW; Lovric VA; Raftos JE; Stewart IM Br J Haematol; 1985 Nov; 61(3):385-92. PubMed ID: 4063202 [TBL] [Abstract][Full Text] [Related]
11. Abnormal phosphoenolpyruvate transport in erythrocytes of hereditary spherocytosis. Ideguchi H; Hamasaki N; Ikehara Y Blood; 1981 Sep; 58(3):426-30. PubMed ID: 7259833 [TBL] [Abstract][Full Text] [Related]
12. Intracellular calcium: lack of effect on ovine red cells. Eaton JW; Berger E; Nelson D; White JG; Rundquist O Proc Soc Exp Biol Med; 1978 Mar; 157(3):506-10. PubMed ID: 345286 [No Abstract] [Full Text] [Related]
13. Abnormal parachloromercuriphenylsulfonate-sensitive cation channel in the erythrocytes of hereditary spherocytosis. Kitao T; Hattori K; Takeshita M Blood; 1976 Apr; 47(4):651-5. PubMed ID: 177134 [TBL] [Abstract][Full Text] [Related]
14. 31P NMR study of erythrocytes from a patient with hereditary pyrimidine-5'-nucleotidase deficiency. Swanson MS; Angle CR; Stohs SJ; Wu ST; Salhany JM; Eliot RS; Markin RS Proc Natl Acad Sci U S A; 1983 Jan; 80(1):169-72. PubMed ID: 6296865 [TBL] [Abstract][Full Text] [Related]
15. [Analysis of the form and size of erythrocytes in healthy children and those with hereditary spherocytosis by the method of holographic interferometry]. Metelkin AN; Manin VN; Rumiantsev AG Pediatriia; 1980; (5):43-5. PubMed ID: 6994061 [No Abstract] [Full Text] [Related]
16. Hereditary spherocytosis: ionophore treatment of erythrocytes in vitro. Szibor R; Petermann H; Wenz I; Steinbicker V; Till U; Nahrendorf C; Mittler U; Hermann J Acta Biol Med Ger; 1982; 41(9):781-6. PubMed ID: 6299036 [No Abstract] [Full Text] [Related]
17. Atypical spherocytosis, a disease of spleen as well as of red blood-cells. Garwicz S Lancet; 1975 Apr; 1(7913):956-7. PubMed ID: 48127 [TBL] [Abstract][Full Text] [Related]
18. Intra- and extraerythrocyte pH at 37 degrees C and during long term storage at 4 degrees C: 31P NMR measurements and an electrochemical model of the system. Raftos JE; Chapman BE; Kuchel PW; Lovric VA; Stewart IM Haematologia (Budap); 1986; 19(4):251-68. PubMed ID: 3817608 [TBL] [Abstract][Full Text] [Related]
19. Membrane lipid depletion in hyperpermeable red blood cells: its role in the genesis of spherocytes in hereditary spherocytosis. Jacob HS J Clin Invest; 1967 Dec; 46(12):2083-94. PubMed ID: 6074008 [TBL] [Abstract][Full Text] [Related]