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Journal Abstract Search

193 related items for PubMed ID: 6760258

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  • 2. [Glucosephosphate dehydrogenase deficiency in erythrocytes and leukocytes of patients with congenital nonspherocytic hemolytic anemia and favism].
    Jabłońska-Skwiecińska E, Staniszewska K.
    Pol Tyg Lek; 1988 Feb 15; 43(7):207-9. PubMed ID: 3405890
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  • 3. Membrane lipid components of normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes of asymptomatic and favic subjects.
    De Flora A, Morelli A, Benatti U, Pontremoli S, Melloni E, Salamino F, Sparatore B, Michetti M, Meloni T.
    Acta Biol Med Ger; 1981 Feb 15; 40(4-5):563-70. PubMed ID: 7315104
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  • 4. [Erythrocyte antioxidant enzymatic systems and serum beta-glucuronidase in subjects with favism. Preliminary results].
    Frigerio R, Sole G, Olla N, Lovicu M, Pigheddu D, Sessini AP, Passiu G, Carcassi U.
    Ann Ital Med Int; 1988 Feb 15; 3(2):87-92. PubMed ID: 3152848
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  • 8. [Favism - a familial enzymatic defect of the red blood cells in a 7-year-old girl].
    Pohorecka J, Jabłońska-Skwiecińska E, Powiertowska-Ryszka G.
    Pediatr Pol; 1982 Feb 15; 57(9):731-4. PubMed ID: 7170153
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  • 9. [Glucose-6-phosphate dehydrogenase activity in the erythrocytes of children with favism, during and at various intervals after the hemolytic attack].
    Tunioli AM.
    Boll Soc Ital Biol Sper; 1964 Dec 31; 40(24):1734-7. PubMed ID: 5877918
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  • 11. Haemopexin behaviour in an acute hyperhaemolytic crisis secondary to favism (erythrocyte glucose-6-phosphate dehydrogenase deficiency).
    Atzeni E, Binaghi F, Pitzus F.
    Ric Clin Lab; 1977 Dec 31; 7(1):39-43. PubMed ID: 866908
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  • 15. Evidence for an effect on erythrophilic IgG-globulin coat by the haemolytic process.
    Thomaidis T, Valassi-Adam H, Matsaniotis N.
    Clin Chim Acta; 1974 Dec 02; 57(2):109-14. PubMed ID: 4434634
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  • 16. Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.
    Rozynkowa D, Gebala A, Zagórski Z.
    Pol Med J; 1970 Dec 02; 9(5):1093-9. PubMed ID: 5510280
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  • 20. [Hemolysis in congenital G-6-PD deficiency. Description of 2 cases with different clinical and laboratory findings].
    Norelli MT, Lumare A.
    Minerva Pediatr; 1970 Dec 01; 22(48):2369-81. PubMed ID: 5503295
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