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43. [The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia]. Burzyńska B; Adamowicz-Salach A; Płochocka D; Gołaszewska E; Witos I Med Wieku Rozwoj; 2009; 13(2):136-9. PubMed ID: 19837994 [TBL] [Abstract][Full Text] [Related]
44. An erythroid-specific exon is present in the human hexokinase gene. Ruzzo A; Andreoni F; Magnani M Blood; 1998 Jan; 91(1):363-4. PubMed ID: 9414310 [No Abstract] [Full Text] [Related]
45. Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency". Beutler E; Forman L; Rios-Larrain E Am J Med; 1987 Nov; 83(5):899-904. PubMed ID: 3674096 [TBL] [Abstract][Full Text] [Related]
46. [Hereditary nonspherocytic hemolytic anemia caused by a deficiency in erythrocytic hexokinase associated with glycogenosis of muscles]. Badalian OL; Bondarenko ES; Ermil'chenko GV; Idel'son LI; Sitnikov VF; Kharit IO Klin Med (Mosk); 1970 Aug; 48(8):156-63. PubMed ID: 5273487 [No Abstract] [Full Text] [Related]
47. Red blood cell PK deficiency: An update of PK-LR gene mutation database. Canu G; De Bonis M; Minucci A; Capoluongo E Blood Cells Mol Dis; 2016 Mar; 57():100-9. PubMed ID: 26832193 [TBL] [Abstract][Full Text] [Related]
48. Residual pyruvate kinase activity in PKLR-deficient erythroid precursors of a patient suffering from severe haemolytic anaemia. Klei TRL; Kheradmand Kia S; Veldthuis M; Beuger BM; Geissler J; Dehbozorgian J; Karimi M; van Bruggen R; van Zwieten R Eur J Haematol; 2017 Jun; 98(6):584-589. PubMed ID: 28295642 [TBL] [Abstract][Full Text] [Related]
49. Rabbit red blood cell hexokinase. Mechanism of decay during cell life-span. Magnani M; Stocchi V; Dacha M; Fornaini G Biomed Biochim Acta; 1983; 42(11-12):S311-6. PubMed ID: 6675710 [TBL] [Abstract][Full Text] [Related]
50. [Hexokinase isoenzymes in normal erythrocytes of adults and newborns and in various hyperregenerative anemias]. Tillmann W; Schröter W Klin Wochenschr; 1969 Jul; 47(14):772-8. PubMed ID: 5382557 [No Abstract] [Full Text] [Related]
51. The molecular basis of disorders of red cell enzymes. McMullin MF J Clin Pathol; 1999 Apr; 52(4):241-4. PubMed ID: 10474511 [No Abstract] [Full Text] [Related]
57. Functional organization and evolution of mammalian hexokinases: mutations that caused the loss of catalytic activity in N-terminal halves of type I and type III isozymes. Tsai HJ Arch Biochem Biophys; 1999 Sep; 369(1):149-56. PubMed ID: 10462451 [TBL] [Abstract][Full Text] [Related]
58. Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia. Kraus AP; Langston MF; Lynch BL Biochem Biophys Res Commun; 1968 Jan; 30(2):173-7. PubMed ID: 4230542 [No Abstract] [Full Text] [Related]
59. A new glucose-6-phosphate dehydrogenase variant (G6PD Iwate) associated with congenital non-spherocytic hemolytic anemia. Kanno H; Takano T; Fujii H; Tani K; Morisaki T; Hirono A; Kumakawa T; Ogura H; Takahashi K; Tsutsumi H Nihon Ketsueki Gakkai Zasshi; 1988 Jul; 51(4):715-9. PubMed ID: 3201886 [No Abstract] [Full Text] [Related]
60. Study of the molecular defects in pyruvate kinase deficient patients affected by nonspherocytic hemolytic anemia. Baronciani L; Magalhães IQ; Mahoney DH; Westwood B; Adekile AD; Lappin TR; Beutler E Blood Cells Mol Dis; 1995; 21(1):49-55. PubMed ID: 7655861 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]