Browsing by Subject Hemoglobin

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Showing results 19 to 38 of 57 < previous   next >
Issue DateTitleAuthor(s)
1991Haemoglobin : model strategies for molecular diseaseScerri, Christian A.; Felice, Alex
2019Haemoglobin point-of-care testingScicluna, Martina
2019-10Haemoglobin point-of-care testingScicluna, Martina; Wirth, Francesca; Azzopardi, Lilian M.
1981Hb G-Philadelphia in asociation with Hb S and α-Thalassemia-2Felice, Alex; Ozdonmez, R.; Headlee, M. E.; Huisman, T. H. J.
1978Hb P Nilotic – β0 thalassemia : mutation of a human hemoglobin regulatory gene?Felice, Alex; Abu-sin, Ahmed; Huisman, T. H. J.
1979Hb P-Nilotic in association with βo-thalassemia : cis-mutation of a hemoglobin βa chain regulatory determinant?Abu-sin, Ahmed; Felice, Alex; Gravely, M. E.; Wilson, J. B.; Reese, A. L.; Lam, H.; Miller, A.; Huisman, T. H. J.
1984Hb synthesis of human leukemia derived cell linesFelice, Alex; Marino, E. M.; Kraus, J.; McKie, Virgil C.
1989Hb Valletta [α2β287(F3)Thr→Pro] and Hb F-Malta-I [α2Gγ2117 (619)His→Arg] are in linkage in the Maltese population.Felice, Alex; Grech, J. L.; Bannister, W. H.; Kutlar, F.; Kutlar, A.; Wilson, J. B.; Webber, B. B.; Hu, H.; Huisman, T. H. J.
1987Heart disease in thalassemia heterozygotes with sickle cell anemiaCovitz, Wesley; Felice, Alex; Milner, Paul F.; McKie, Virgil C.; McKie, Kathleen M.; Strong, William B.; Davis, Harry C.
1983Hemoglobin production on stimulation of K562 human pluripotent leukemia cellsFelice, Alex; Mayson, S. M.; Reese, A. L.; Huisman, T. H. J.
1987Hemolytic anemia due to heterozygosity for Hb C, α+-Thalassemia and hereditary xerocytosisFelice, Alex; Abraham, M.; Bockman, D.; McKie, Virgil C.; Greenberg, M.
1987Hemorheologic parameters in children with homozygous Sickle Cell Anemia receiving chronic red cell transfusions for large cerebral vessel vasculopathy (LCVV)KcKie, V.; KcKie, K. M.; Jeraldo, T. L.; Adams, R. A.; Felice, Alex
1988Hemorheologic parameters in children with homozygous Sickle Cell Anemia receiving chronic red cell transfusions for large cerebral vessel vasculopathy (LCVV)Sabio, H.; McKie, Virgil C.; McKie, Kathleen M.; Jeraldo, T. L.; Adams, R. A.; Felice, Alex
1970Hereditary diaphorase deficiency methemoglobinemia in Maltese familiesVassallo, Luis A.; Cauchi, Maurice N.
1980In vitro synthesis of hemoglobin in BFU-e derived colonies of persons with an α or a β-ThalassemiaFelice, Alex; Altay, C. A.; Reese, A. L.; Webber, B.; Huisman, T. H. J.
2000In vivo expression of the G γ globin gene of foetal haemoglobinPulis, Svetlana
2009The influence of dietary intake on blood glucose control in children with type 1 diabetes mellitus.Agius, Doriette
1989Interview with Professor Frank Vella and Professor Alex FeliceFelice, Alex; Vella, Frank
2018Intravenous and subcutaneous Epoetin administration in the maintenance of optimal haemoglobin levels in end-stage renal failure patients on haemodialysisSpiteri, Melanie Ann
2012Investigating the frequency of the G23D mutation causing DHPR deficiency in the Maltese population.Tabone, Christine