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PUBMED FOR HANDHELDS

Journal Abstract Search


219 related items for PubMed ID: 5969464

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  • 3. [Favism (study of 8 families)].
    Cintado Bueno C, Sosa Alamo R, Plaza Delgado E, Toro Ortega J, Santos Soto J, Fernández Palacios F.
    An Esp Pediatr; 1978 May; 11(5):419-26. PubMed ID: 697214
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  • 4. [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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  • 10. Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.
    Rozynkowa D, Gebala A, Zagórski Z.
    Pol Med J; 1970 Feb 15; 9(5):1093-9. PubMed ID: 5510280
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  • 11. Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Poland--a study on the 563 and 1311 mutations of the G6PD gene.
    Jabłońska-Skwiecińska E, Zimowski JG, Kłopocka J, Bisko M, Hoffman-Zacharska D, Zaremba J.
    Eur J Hum Genet; 1997 Feb 15; 5(1):22-4. PubMed ID: 9156317
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  • 12. Hemolytic crises of favism in Sicilian females heterozygous for G-6-PD deficiency.
    Russo G, Mollica F, Pavone L, Schilirò G.
    Pediatrics; 1972 Jun 15; 49(6):854-9. PubMed ID: 5041319
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  • 14. Electrophoretic heterogeneity of erythrocyte and leucocyte glucose-6-phosphate dehydrogenase in Italians from various ethnic groups.
    Bonsignore A, Fornaini G, Leoncini G, Fantoni A.
    Nature; 1966 Aug 20; 211(5051):876-7. PubMed ID: 5968777
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  • 15. [Favism: hemolytic crisis due to glucose-6-phosphate dehydrogenase deficiency in erythrocytes].
    Sroczyńska M, Sychlowy A.
    Pol Tyg Lek; 1973 May 14; 28(20):744-5. PubMed ID: 4709398
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  • 16. [Favism in Polish families].
    Jabłońska-Skwiecińska E, Pogłód R, Skrobowska A.
    Pol Tyg Lek; 1973 May 14; 45(38-39):778-81. PubMed ID: 2095545
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  • 17. [Characterization of glucose-6-phosphate dehydrogenase (G-6-PD) in granulocytes and lymphocytes of normal and enzyme deficient Sardinians].
    Fiorelli G, Idéo G.
    Quad Sclavo Diagn; 1971 Mar 14; 7(1):118-33. PubMed ID: 5155174
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  • 18. 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 Mar 14; 7(1):39-43. PubMed ID: 866908
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  • 19. [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 Mar 14; 57(9):731-4. PubMed ID: 7170153
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