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Journal Abstract Search

186 related items for PubMed ID: 6426235

  • 1. Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza).
    Ventura A, Panizon F, Soranzo MR, Veneziano G, Sansone G, Testa U, Luzzatto L.
    Acta Haematol; 1984; 71(4):227-34. PubMed ID: 6426235
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  • 2. Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.
    Gangarossa S, Romano V, Miraglia del Giudice E, Perrotta S, Iolascon A, Schiliro G.
    Acta Haematol; 1995; 93(1):36-9. PubMed ID: 7725848
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  • 3. A congenital dyserythropoietic anaemia variant presenting as hydrops fetalis.
    Carter C, Darbyshire PJ, Wickramasinghe SN.
    Br J Haematol; 1989 Jun; 72(2):289-90. PubMed ID: 2757972
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  • 4. G6Pd Kanazawa: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Kitao T, Ito K, Hattori K, Matsuki T, Yoneyama Y.
    Acta Haematol; 1982 Jun; 68(2):131-5. PubMed ID: 6812368
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  • 5. Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia.
    Alfinito F, Calabro V, Cappellini MD, Fiorelli G, Filosa S, Iolascon A, Miraglia del Giudice E, Perrotta S, Migliorati R, Vallone D.
    Br J Haematol; 1994 May; 87(1):148-52. PubMed ID: 7947239
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  • 6. Chronic haemolytic anaemia and glucose-6 phosphate dehydrogenase deficiency. Case report and review of the literature.
    Hundsdoerfer P, Vetter B, Kulozik AE.
    Acta Haematol; 2002 May; 108(2):102-5. PubMed ID: 12187030
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  • 9. Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum.
    Vives-Corrons JL, Pujades MA, Petit J, Colomer D, Corbella M, Aguilar i Bascompte JL, Merino A.
    Hum Genet; 1989 Jan; 81(2):161-4. PubMed ID: 2912886
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  • 13. Nonimmune hydrops fetalis caused by G6PD deficiency hemolytic crisis and congenital dyserythropoietic anemia.
    Molad M, Waisman D, Rotschild A, Auslander R, Kessel I, Soloviechick M, Goldberg Y, Shabad E.
    J Perinatol; 2013 Jun; 33(6):490-1. PubMed ID: 23719252
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  • 17. Ultrastructural, cell culture and karyotype study of bone marrow in a patient with congenital dyserythropoietic anaemia (CDA)-type III presenting with recurrent still-births.
    Ghosh K, Yavagal D, Phillips C, Jijina F, Pathare AV, Kerketta L, Iyer YS, Nair CN, Shinde S, Mohanty D.
    Haematologia (Budap); 1998 Jun; 29(1):41-5. PubMed ID: 9704256
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  • 19. Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an Italian family.
    Arnold H, Löhr GW, Hasslinger K, Ludwig R.
    Hum Genet; 1981 Jun; 57(2):226-9. PubMed ID: 7228040
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