Showing results 24 to 43 of 81
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| Issue Date | Title | Author(s) |
| 2007 | Gene-environment interactions in parkinsonism and Parkinson’s disease | Dick, Finlay D.; Palma, Giuseppe de; Ahmadi, Ahmad; Osborne, Aileen; Scott, Neil W.; Prescott, Gordon James; Bennett, Jami; Semple, Sean; Dick, Smita; Mozzoni, Paola; Haites, Neva E.; Bezzina Wettinger, Stephanie; Mutti, Antonio; Otelea, M.; Seaton, Anthony W. H.; Soderkvist, Peter; Felice, Alex E. |
| 2016 | Genetic causes of Parkinson’s disease in the Maltese : a study of selected mutations in LRRK2, MTHFR, QDPR and SPR | Zahra, Charmaine; Tabone, Christine; Camilleri, Graziella; Felice, Alex E.; Farrugia, Rosienne; Bezzina Wettinger, Stephanie |
| 2015-12 | Genetic determinants of visceral adiposity in Type 2 diabetes mellitus | Pace, Nikolai Paul; Vassallo, Josanne; Felice, Alex E. |
| 2011 | Genetic factors in risk assessment for the development of type 2 diabetes mellitus in a small case series | Abou-Hussein, S.; Savona-Ventura, Charles; Grima, Stephen; Felice, Alex E. |
| 2013 | Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy | Tafrali, Christina; Paizi, Arsinoi; Borg, Joseph; Radmilovic, Milena; Bartsakoulia, Marina; Giannopoulou, Emily; Giannakopoulou, Olga; Stojiljkovic-Petrovic, Maja; Zukic, Branka; Poulas, Konstantinos; Stavrou, Eleana F.; Lambropoulou, Polyxeni; Kourakli, Alexandra; Felice, Alex E.; Papachatzopoulou, Adamantia; Philipsen, Sjaak; Pavlovic, Sonja; Georgitsi, Marianthi; Patrinos, George P. |
| 2013 | The genomics of type 2 diabetes : the Maltese contribution | Pace, Nikolai Paul; Vassallo, Josanne; Felice, Alex E. |
| 2010 | Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin | Borg, Joseph; 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 E.; 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 E.; Huisman, Titus Hendrik Jan |
| 1978 | Hb Nottingham (α;2β;2 (FG5) 98 VAL→GLY) in a Caucasian male : clinical and biosynthetic studies | Orringer, Eugene P.; Felice, Alex E.; Reese, A. L.; Wilson, Jerry B.; Lam, H. L.; Gravely, Marsha E.; Huisman, Titus Hendrik Jan |
| 1980 | Hb S, Hb G-Philadelphia and α-thalassemia-2 in a Black family | Felice, Alex E.; 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 E. |
| 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 E. |
| 1987 | Heart disease in thalassemia heterozygotes with sickle cell anemia | Covitz, Wesley; Felice, Alex E.; Milner, Paul F.; McKie, Virgil C.; McKie, Kathleen Mood; Strong, William B.; Davis, Harry C. |
| 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 E. |
| 2016-04 | The hidden history of the Maltese genome | Wilcockson, Scott; Felice, Alex E.; Borg, Joseph; Mizzi, Clint |
| 1982 | Identification and quantitation of embryonic and three types of fetal hemoglobin produced on induction of the human pluripotent leukemia cell line K‐562 with hemin | Fuhr, Josephy E.; Bamberger, Elena G.; Lozzio, Carmen B.; Lozzio, Bismarck B.; Felice, Alex E.; Altay, Gultekin; Webber, Brooke B.; Reese, A. L.; Mayson, Sylvia M.; Huisman, Titus Hendrik Jan |
| 2018-05-15 | Identification of an HNF1B p.Arg527Gln mutation in a Maltese patient with atypical early onset diabetes and diabetic nephropathy | Pace, Nikolai Paul; Craus, Johann; Felice, Alex E.; Vassallo, Josanne |
| 1995 | Il-Htiega tar-ricerka xjentifika | Felice, Alex E. |
| 1980 | Interaction of the β chain variant hemoglobin Leslie and the α chain variant hemoglobin Montgomery in a Black female | Huisman, Titus Hendrik Jan; Gravely, Marsha E.; Wilson, Jerry B.; Webber, Brooke B.; Felice, Alex E.; Miller, Augustus |
| 1978 | Is the trimodality of Hb Leslie (α2β2131Gln→ 0) in heterozygotes the result of a variable number of active α‐chain genes? Evidence for posttranslational control of hemoglobin synthesis | Felice, Alex E.; Abraham, Edathara C.; Miller, Augustus; Stallings, M. B.; Huisman, Titus Hendrik Jan |
