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3. Sodium transport across the surface membrane of red blood cells in hereditary spherocytosis. BERTLES JF J Clin Invest; 1957 Jun; 36(6 Part 1):816-24. PubMed ID: 13439021 [No Abstract] [Full Text] [Related]
4. THE PHOSPHORYLATED CARBOHYDRATE INTERMEDIATES FROM ERYTHROCYTES IN HEREDITARY SPHEROCYTOSIS. SHAFER AW Blood; 1964 Apr; 23():417-26. PubMed ID: 14138234 [No Abstract] [Full Text] [Related]
5. CHANGES IN THE CONTENT AND 32P INCORPORATION OF GLYCOLYTIC INTERMEDIATES DURING INCUBATION OF NORMAL AND HEREDITARY SPHEROCYTOSIS ERYTHROCYTES. KEITT AS Br J Haematol; 1965 Mar; 11():177-87. PubMed ID: 14262176 [No Abstract] [Full Text] [Related]
6. Inhibition of P32-orthophosphate exchange by sodium fluoride in erythrocytes from patients with hereditary spherocytosis. ALTMAN KI; TABECHIAN H; YOUNG LE Proc Soc Exp Biol Med; 1956; 92(4):712-3. PubMed ID: 13370503 [No Abstract] [Full Text] [Related]
7. Studies on the pathogenesis of haemolysis in hereditary spherocytosis. PRANKERD TA Q J Med; 1960 Apr; 29():199-208. PubMed ID: 14434645 [No Abstract] [Full Text] [Related]
8. Studies on the survival of transfused erythrocytes in hereditary spherocytosis and acquired hemolytic anemia. WRIGHT CS; BOURONCLE BA; BUBIS SR; DOAN CA J Lab Clin Med; 1950 Dec; 36(6):1006-7. PubMed ID: 14795106 [No Abstract] [Full Text] [Related]
9. STUDIES ON THE ANTIGENS OF HUMAN RED CELL GHOSTS. DIFFERENCES IN ANTIGENIC SPECIFICITY OF HUMAN NORMAL ADULT, HEREDITARY SPHEROCYTOSIS AND AUTO-IMMUNE HAEMOLYTIC ANAEMIA S PROTEIN. VULPIS N Acta Haematol; 1963 Nov; 30():280-7. PubMed ID: 14073429 [No Abstract] [Full Text] [Related]
10. Megaloblastic anaemia in congenital spherocytosis. DELAMORE IW; RICHMOND J; DAVIES SH Br Med J; 1961 Feb; 1(5225):543-5. PubMed ID: 13721430 [No Abstract] [Full Text] [Related]
11. Intraerythrocytic metabolic failure in the hereditary spherocytosis as reflected by the shape of the frequency distribution curve of resistance to hypotonicity in the erythrocyte population. TEITEL P Folia Haematol Int Mag Klin Morphol Blutforsch; 1960; 77():212-3. PubMed ID: 13837297 [No Abstract] [Full Text] [Related]
12. Multiple inherited erythrocyte abnormalities in an American Negro family: hereditary spherocytosis, sickling and thalassemia. COHEN F; ZUELZER WW; NEEL JV; ROBINSON AR Blood; 1959 Jul; 14(7):816-27. PubMed ID: 13662326 [No Abstract] [Full Text] [Related]
13. Some aspects of porphyrin metabolism in hereditary spherocytosis and in acquired haemolytic anaemias. PRATO V; RUBINO GF; MAZZA U; RASETTI L Panminerva Med; 1962 Sep; 4():391-3. PubMed ID: 13985968 [No Abstract] [Full Text] [Related]
14. THREE INHERITED INTRA-ERYTHROCYTIC DEFECTS: HEREDITARY SPHEROCYTOSIS, HB S AND HB C. THOMPSON RB; ROBERTSON MG Acta Haematol; 1964 Oct; 32():233-8. PubMed ID: 14252557 [No Abstract] [Full Text] [Related]
15. Abnormal phosphoenolpyruvate transport in erythrocytes of hereditary spherocytosis. Ideguchi H; Hamasaki N; Ikehara Y Acta Biol Med Ger; 1981; 40(4-5):555-8. PubMed ID: 7315102 [TBL] [Abstract][Full Text] [Related]
16. Hereditary spherocytosis. I. Clinical, hematologic and genetic features in 28 cases, with particular reference to the osmotic and mechanical fragility of incubated erythrocytes. YOUNG LE; IZZO MJ; PLATZER RF Blood; 1951 Nov; 6(11):1073-98. PubMed ID: 14869368 [No Abstract] [Full Text] [Related]
17. Megaloblastic erythropoiesis in congenital spherocytic anaemia. BARR JB; NICOLL WD Scott Med J; 1959 Dec; 4():563-6. PubMed ID: 13797008 [No Abstract] [Full Text] [Related]
18. [Hereditary spherocytic anemia with hypersplenomegaly, crural ulcer and biliary lithiasis. Steroid-splenectomy treatment. Clinical, hematological and erythrokinetic observations]. MARMONT A; BIASSONI P; NEGRINI A Minerva Med; 1961 May; 52():1764-77. PubMed ID: 13767011 [No Abstract] [Full Text] [Related]