Showing results 44 to 63 of 129
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| Issue Date | Title | Author(s) |
| 1991 | Haemoglobin : model strategies for molecular disease | Scerri, Christian A.; Felice, Alex |
| 1975 | Haemoglobin abnormalities in the Maltese | Felice, Alex |
| 2010 | Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin | Borg, Joseph J.; Papadopoulos, Petros; Georgitsi, Marianthi; Gutierrez, Laura; Grech, Godfrey; Fanis, Pavlos; Phylactides, Marios; Verkerk, Annemieke J.M.H.; van der Spek, Peter J.; Scerri, Christian A.; Cassar, Wilhelmina; Galdies, Ruth; van IJcken, Wilfred; Ozgur, Zeliha; Gillemans, Nynke; Hou, Jun; Bugeja, Marisa; Grosveld, Frank G.; von Lindern, Marieke; Felice, Alex; Patrinos, George P.; Philipsen, Sjaak |
| 1989 | Hb Evans or α262 (E11) Val→ Metβ2 ; an unstable hemoglobin causing a mild hemolytic anemia | Wilson, Jerry B.; Webber, Brooke B.; Kutlar, Abdullah; Reese, A. L.; McKie, Virgil C.; Lutcher, Charles Lawrence; Felice, Alex; Huisman, Titus Hendrik Jan |
| 1981 | Hb G-Philadelphia in asociation with Hb S and α-Thalassemia-2 | Felice, Alex; Ozdonmez, R.; Headlee, M. E.; Huisman, T. H. J. |
| 1978 | Hb Nottingham (α;2β;2 (FG5) 98 VAL→GLY) in a Caucasian male : clinical and biosynthetic studies | Orringer, Eugene P.; Felice, Alex; Reese, A. L.; Wilson, Jerry B.; Lam, H. L.; Gravely, Marsha E.; Huisman, Titus Hendrik Jan |
| 1978 | Hb P Nilotic – β0 thalassemia : mutation of a human hemoglobin regulatory gene? | Felice, Alex; Abu-sin, Ahmed; Huisman, T. H. J. |
| 1979 | Hb 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. |
| 1980 | Hb S, Hb G-Philadelphia and α-thalassemia-2 in a Black family | Felice, Alex; Mayson, Sylvia M.; Webber, Brooke B.; Miller, Augustus; Gravely, Marsha E.; Huisman, Titus Hendrik Jan |
| 1997 | HB Setif [A94(Gi)Asp+Tyr] in Malta | Borg, Isabella; Valentino, Mario; Fiorini, A.; Felice, Alex |
| 1984 | Hb synthesis of human leukemia derived cell lines | Felice, Alex; Marino, E. M.; Kraus, J.; McKie, Virgil C. |
| 1989 | Hb 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. |
| 2010 | Hb Valletta [β87 (F3) Thr→ Pro] and Hb Marseille/Long Island [β2 (NA2) His→ Pro;(–1) Met-(+ 1) Val-(+ 2) Pro-Leu], in a unique compound heterozygote with a normal hemoglobin phenotype | Galdies, Ruth; Cassar, Wilhelmina; Pizzuto, Monica; Scerri, Christian A.; Felice, Nicholas; Cassar, Olivianne A.; Buttigieg, George; Felice, Alex |
| 1987 | Heart disease in thalassemia heterozygotes with sickle cell anemia | Covitz, Wesley; Felice, Alex; Milner, Paul F.; McKie, Virgil C.; McKie, Kathleen Mood; Strong, William B.; Davis, Harry C. |
| 1987 | Heart disease in thalassemia heterozygotes with sickle cell anemia | Covitz, Wesley; Felice, Alex; Milner, Paul F.; McKie, Virgil C.; McKie, Kathleen M.; Strong, William B.; Davis, Harry C. |
| 1983 | Hemoglobin production on stimulation of K562 human pluripotent leukemia cells | Felice, Alex; Mayson, S. M.; Reese, A. L.; Huisman, T. H. J. |
| 1987 | Hemolytic anemia due to heterozygosity for Hb C, α+-Thalassemia and hereditary xerocytosis | Felice, Alex; Abraham, M.; Bockman, D.; McKie, Virgil C.; Greenberg, M. |
| 1989 | Hemorheologic parameters in children with homozygous sickle cell anemia receiving chronic red cell transfusions for large cerebral vessel vasculopathy | Sabio, Hernan; McKie, Virgil C.; McKie, Kathleen Mood; Jeraldo, T. L.; Adams, R. A.; Felice, Alex |
| 1987 | Hemorheologic 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 |
| 1988 | Hemorheologic 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 |
