Showing results 18 to 37 of 129
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| Issue Date | Title | Author(s) |
| 1984 | Deletions and duplications of α or ζ globin genes in children with sickle cell anemia | Felice, Alex; McKie, Virgil C.; McKie, Kathleen M.; Huisman, T. H. J. |
| 1986 | Dense cell formation in pediatric and adolescent patients with sickle cell disease | Abraham, E. C.; Bergherm, B.; Felice, Alex; McKie, Virgil C.; Abraham, A.; McKie, Kathleen M. |
| 1977 | Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults | Altay, Gultekin; Garver, Fred A.; Bannister, William H.; Grech, Joseph L.; Huisman, Titus Hendrik Jan; Felice, Alex |
| 2006 | Detection of new genomic landmarks in the Maltese goat using Rapd PCR | Blundell, Renald; Felice, Alex |
| 1992 | The development of a comprehensive genetics programme for the early identification of disabled children with hereditary disease | Felice, Alex |
| 2007 | Developmental effect of the XmnI site on Gγ-globin gene expression among newborn Hb F-Malta-I [Gγ117 (G19) His→ Arg, CAT→ CGT] heterozygotes and adult β+-thalassemia homozygotes | Pulis, Svetlana; Scerri, Christian A.; Schembri-Wismayer, Pierre; Galdies, Ruth; Bezzina Wettinger, Stephanie; Felice, Alex |
| n.d. | Developmental hematology of homozygous HB C disease | McKie, Virgil C.; McKie, Kathleen M.; Kutlar, A.; Felice, Alex |
| 1985 | Developmental hematology of SS and SC disease in association with α-thalassemia-2 | Felice, Alex; Marino, E. M.; McKie, Kathleen M.; McKie, Virgil C. |
| 1986 | Different ζ globin gene deletions among Black Americans | Felice, Alex; Cleek, M. P.; Marino, E. M.; McKie, Kathleen Mood; McKie, Virgil C.; Chang, B. K.; Huisman, Titus Hendrik Jan |
| 2011 | Does quantitative heterogeneity of human fetal hemoglobin (Hb F) reveal friends or foes of KLF1 in globin gene switching? | Felice, Alex; Galdies, Ruth; Borg, Joseph J.; Grech, Godfrey; Cassar, Wilhelmina; Scerri, Christian A.; Patrinos, George P.; Philipsen, Sjaak |
| 1984 | The effect of deletions and reduplications on the expression of human α and ζ globin genes | Felice, Alex; McKie, Kathleen M.; McKie, Virgil C.; Huisman, T. H. J. |
| 2009 | An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies : the Euro-Mediterranean ITHANET project | Lederer, Carsten W.; Basak, Ayse Nazli; Aydinok, Yesim; Christou, Soteroula; El-Beshlawy, Amal; Eleftheriou, Androulla; Fattoum, Slaheddine; Felice, Alex; Fibach, Eitan; Galanello, Renzo; Gambari, Roberto; Gavrila, Lucian; Giordano, Piero C.; Grosveld, Frank G.; Hassapopoulou, Helen; Hladka, Eva; Kanavakis, Emmanuel; Locatelli, Franco; Old, John; Patrinos, George P.; Romeo, Giovanni; Taher, Ali; Traeger-Synodinos, Joanne; Vassiliou, Panayiotis; Villegas, Ana; Voskaridou, Ersi; Wajcman, Henri; Zafeiropoulos, Anastasios; Kleanthous, Marina |
| 2007 | Environmental risk factors for Parkinson’s disease and Parkinsonism : the Geoparkinson study | Dick, Finlay D.; Palma, Giuseppe de; Ahmadi, Ahmad; Scott, Neil W.; Prescott, Gordon James; Bennett, Jami; Semple, Sean; Dick, Smita; Counsell, Carl E.; Mozzoni, Paola; Haites, Neva E.; Bezzina Wettinger, Stephanie; Mutti, Antonio; Otelea, M.; Seaton, Anthony W.H.; Soderkvist, Peter; Felice, Alex; Borg, Joseph J.; Scerri, Christian A.; The Geoparkinson study group |
| 2011 | Erythroid phenotypes associated with KLF1 mutations | Borg, Joseph J.; Patrinos, George P.; Felice, Alex; Philipsen, Sjaak |
| 1987 | Erythropoiesis inhibitory factor(s) in polycythemia vera | Lewis, J. P.; Faguet, G. B.; Tsai, J. F. L.; Felice, Alex |
| 2002 | The ethics of pre-implantation genetic diagnosis | Felice, Alex |
| 2015 | The EuroBioBank Network : ten years of hands-on experience of collaborative, transnational biobanking for rare diseases | Mora, Marina; Angelini, Corrado; Bignami, Fabrizia; Bodin, Anne-Mary; Crimi, Marco; Di Donato, Jeanne-Helene; Felice, Alex; Jaeger, Cecile; Karcagi, Veronika; LeCam, Yann; Lynn, Stephen; Meznaric, Marija; Moggio, Maurizio; Monaco, Lucia; Politano, Luisa; Posada De La Paz, Manuel; Saker, Safaa; Schneiderat, Peter; Ensini, Monica; Garavaglia, Barbara; Gurwitz, David; Johnson, Diana; Muntoni, Francesco; Puymirat, Jack; Reza, Mojgan; Voit, Thomas; Baldo, Chiara; Bricarelli, Franca Dagna; Goldwurm, Stefano; Merla, Giuseppe; Renieri, Alessandro; Zatloukal, Kurt; Filocamo, Mirella; Lochmuller, Hanns; Pegoraro, Elena |
| 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; Borg, Joseph J.; Scerri, Christian A.; The Geoparkinson Study Group |
| 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; Farrugia, Rosienne; Bezzina Wettinger, Stephanie |
| 2015-12 | Genetic determinants of visceral adiposity in Type 2 diabetes mellitus | Pace, Nikolai Paul; Vassallo, Josanne; Felice, Alex |
