Browsing by Author Felice, Alex E.

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Issue DateTitleAuthor(s)
2004Novel polymorphisms influencing transcription of the human CHRM2 gene in airway smooth muscleFenech, Anthony G.; Billington, Charlotte K.; Swan, Caroline; Richards, Susan; Hunter, Therese; Ebejer, Martin J.; Felice, Alex E.; Ellul-Micallef, Roger; Hall, Ian P.
1979Observations on the calculated contents of variant and normal α chains in adult and fetal erythrocytesFelice, Alex E.; Huisman, Titus Hendrik Jan
1981The occurrence and identification of α-thalassemia-2 among hemoglobin S heterozygotesFelice, Alex E.; Altay, Cigdem A.; Milner, Paul F.; Huisman, Titus Hendrik Jan
2012Optimization of an imaging cytometry protocol to observe the cellular distribution of haemoglobin F in F-erythrocytesScerri, Jeanesse; Felice, Alex E.; Cassar, Wilhelmina; Scerri, Christian; Grech, Godfrey; Galdies, Ruth; Borg, Joseph; Saliba, Christian
1982Organization of α-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, β-thalassemia, and α-thalassemia-2Felice, Alex E.; Ozdonmez, R.; Headlee, M. E.; Huisman, Titus Hendrik Jan
2003Oversight of science and technologyFelice, Alex E.
1973Pilonidal sinuses and their treatmentFelice, Alex E.; Parnis, R. J.
1996Polymerase chain reaction in molecular biotechnology; appropriate technology for developing countriesFelice, Alex E.; Bezzina Alshinawi, Connie
2014A polymorphism in the gene for protein tyrosine phosphatase 1b is associated with altered lipid profile and myocardial infarctionBezzina Wettinger, Stephanie; Doggen, Catharina; Spek, A.; Felice, Alex E.; Reitsma, P. H.; Rosendaal, F. R.
2006Population structure in the Mediterranean basin : a Y chromosome perspectiveCapelli, Cristian; Redhead, Nicola; Romano, Valentino; Cali, Francesco; Lefranc, Gerard; Delague, Valerie Rie; Megarbane, Andre; Felice, Alex E.; Pascali, Vincenzo L.; Neyophytou, Pavlos; Poulli, Z.; Novelletto, Andrea; Malaspina, Patrizia; Terrenato, L.; Berebbi, Alain; Fellous, Marc; Thomas, Mark; Goldstein, David B.
2015-03Rare disease research and the Malta biobankVella, Joanna; Borg, Joseph; Grech, Laura; Galdies, Ruth; Scerri, Jeanesse; Cassar, Wilhelmina; Scerri, Christian; Grech, Godfrey; Soler, Doriette; Said, Edith; Borg, Isabella; Vella, Norbert; Camilleri-Podesta, Marie Therese; Ellul, Bridget; Abela, Mark; Grima, David; Zammit, Esther; Pace, Nikolai Paul; Felice, Alex E.; Said Conti, Valerie
1984The rare α-Thalassemia-1 of Blacks is a ζα-Thalassemia-1 associated with a deletion of all α- and ζ-Globin genesFelice, Alex E.; Cleek, M. P.; McKie, Kathleen Mood; McKie, Virgil C.; Huisman, Titus Hendrik Jan
2003Realising a thriving Maltese biotechnology industry by 2015Galea Agius, Dorita; Felice, Alex E.
2011Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collectionPatrinos, George P.; Al-Aama, Jumana Yousuf; Al-Mulla, Fahd; Borg, Joseph; Devereux, Andrew; Felice, Alex E.; Macrae, Finlay A.; Marafie, Makia J.; Peterson, Michael B.; Qi, Ming; Ramesar, Rajkumar S.; Zlotogora, Joel; Cotton, Richard G. H.; Al Aqeel, Aida
2007A review of cis-trans interplay between DNA sequences 5′ to the Gγ-and β-globin genes among Hb F-Malta-I heterozygotes/homozygotes and β-thalassemia homozygotes/compound heterozygotes, and the effects of hydroxyurea on the Hb F/F-erythrocyte; the need for large multicenter trialsFelice, Alex E.; Borg, Joseph; Pizzuto, Monica; Cassar, Wilhelmina; Galdies, Ruth; Bezzina Wettinger, Stephanie; Pulis, Svetlana; Hunter, Gary J.; Caruana, Mary R.; Farrugia, Mario; Scerri, Christian A.
2012The role of the A C395 IFNGR1 mutation in determining susceptibility to intracellular infection in MaltaAnderson, Suzanne T.; Mangion, Mariella; Newport, Melanie J.; Felice, Alex E.; Hibberd, Martin; Levin, Mike; Attard Montalto, Simon
1996Screening for congenital hypothyroidism in Maltese newborns using cord bloodParascandalo, Raymond; Felice, Alex E.; Rizzo, M.; Vassallo Agius, Paul
2005Sepiapterin reductase deficiency : a congenital dopa-responsive motor and cognitive disorderParascandalo, Raymond; Farrugia, Rosienne; Felice, Alex E.; Neville, Brian G. R.
2012Sepiapterin reductase deficiency : a treatable mimic of cerebral palsyFriedman, Jennifer; Roze, Emmanuel; Abdenur, Jose E.; Chang, Richard; Gasperini, Serena; Saletti, Veronica; Wali, Gurusidheshwar M.; Eiroa, Hernan; Neville, Brian G. R.; Felice, Alex E.; Parascandalo, Raymond; Zafeiriou, Dimitrios I.; Arrabal-Fernandez, Luisa; Dill, Patricia; Eichler, Florian S.; Echenne, Bernard; Gutierrez-Solana, Luis G.; Hoffmann, Georg F.; Hyland, Keith; Kusmierska, Katarzyna; Tijssen, Marina A. J.; Lutz, Thomas; Mazzuca, Michel; Penzien, Johann; Poll-The, Bweetien Tien T.; Sykut-Cegielska, Jolanta; Szymanska, Krystyna; Thony, Beat; Blau, Nenad
2009-11The significance of quantitative HB epidemiology in public health genomics and genetic models of complex diseaseFelice, Alex E.; Galdies, Ruth; Cassar, Wilhelmina; Pizzuto, Monica; Borg, Joseph; Bugeja, Marisa; Caruana, Mary Rose; Farrugia, Mario; Scerri, Christian A.