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Journal Abstract Search

312 related items for PubMed ID: 6162733

  • 1. Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family.
    Horányi M, Szelényi J, Rona G, Lang A, Lehmann H, Hollán SR.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):654-60. PubMed ID: 6162733
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  • 3. Hemoglobin A2, E and F levels and the incidence of hemoglobin E, beta-thalassemia, and glucose-6-phosphate dehydrogenase deficiency in lymphoma.
    Panich V, Na-Nakorn S, Piankijagum A.
    J Med Assoc Thai; 1974 Jan; 57(1):3-10. PubMed ID: 4814776
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  • 5. Anemia in patients with coinherited thalassemia and glucose-6-phosphate dehydrogenase deficiency.
    Pornprasert S, Phanthong S.
    Hemoglobin; 2013 Jan; 37(6):536-43. PubMed ID: 23944358
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  • 6. Effect of alpha thalassaemia, G-6-PD deficiency and Hb F on the nature of sickle cell anaemia in south-western Saudi Arabia.
    el-Hazmi MA, al-Swailem AR, Bahakim HM, al-Faleh FZ, Warsy AS.
    Trop Geogr Med; 1990 Jul; 42(3):241-7. PubMed ID: 1705730
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  • 7. Leg ulcer in a patient with beta-thalassemia and glucose-6-phosphate-dehydrogenase deficiency.
    Lotti T, Benci M, Palleschi GM, Cantini F, Palchetti R, Albertacci A.
    Int J Dermatol; 1990 Jul; 29(6):426-7. PubMed ID: 2397966
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  • 8. Haemolytic anaemia.
    Weatherall DJ.
    Practitioner; 1978 Aug; 221(1322):194-202. PubMed ID: 724613
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  • 9. Spectrum of haemolytic anaemias in Punjab, North India.
    Dash S, Dash RJ.
    Trop Geogr Med; 1980 Dec; 32(4):312-6. PubMed ID: 7210170
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  • 12. Sickle cell haemoglobin, thalassaemia and G-6-PD enzyme deficiency genes in Garasiya tribe inhabited malaria endemic areas of Sirohi District, Rajasthan (India).
    Choubisa SL.
    J Commun Dis; 2009 Mar; 41(1):13-8. PubMed ID: 19886170
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  • 14. [Haemolytic anaemia due to glucose-6-phosphatehydrogenase deficiency in a Slovak family (author's transl)].
    Gocárová K, Strnová J, Sasinka M, Plenta I, Chmeliar J.
    Cas Lek Cesk; 1976 Aug 27; 115(33-34):1031-5. PubMed ID: 975174
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  • 16. Survey on haemoglobin variants, beta-thalassaemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobin types in Turkish people living in Manavgat, Serik and Boztepe (Antalya).
    Aksoy M, Dinçol G, Erdem S.
    Hum Hered; 1980 Aug 27; 30(1):3-6. PubMed ID: 7353885
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  • 17. [Concurrence on two siblings of three haemoglobin abnormal genes: haemoglobin S, beta-thalassaemia and hereditary persistence of foetal haemoglobin (author's transl)].
    Guerrero García R, Rosillo de León J, Landero de Ruíz N, Padilla C, Ruíz Reyes G.
    Sangre (Barc); 1978 Aug 27; 23(5):578-86. PubMed ID: 741340
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  • 18. Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
    Aksoy M, Kutlar A, Kutlar F, Dinçol G, Erdem S, Baştesbihçi S.
    J Med Genet; 1985 Aug 27; 22(4):288-90. PubMed ID: 4045955
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  • 20. Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level.
    Sanna G, Frau F, Melis MA, Galanello R, De Virgiliis S, Cao A.
    Br J Haematol; 1980 Apr 27; 44(4):555-61. PubMed ID: 7378315
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