Browsing by Author Bezzina Wettinger, Stephanie

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Showing results 1 to 12 of 12
Issue DateTitleAuthor(s)
1999Characterization and locus assignment of two α-globin variants present in the Maltese population : Hb St. Luke's [α95 (G2) Pro→ Arg] and Hb Setif [α94 (G1) Asp→ Tyr]Bezzina Wettinger, Stephanie; Galdies, Ruth; Scerri, Christian A.; Felice, Alex E.
2015-07The clinical bank of BBMRI.mtVella, Joanna; Grech, Laura; Scerri, Jeanesse; Scerri, Christian; Bezzina Wettinger, Stephanie; Camilleri, Graziella; Zammit, Esther; Grech, Godfrey; Soler, Doriette; Borg, Isabella; Camilleri Podesta, Marie Therese; Abela, Mark; Ebejer, Jean Paul; Borg, Joseph; Galdies, Ruth; Cassar, Wilhelmina; Camilleri, Alexander; Farrugia, Rosienne; Pace, Nikolai P.; Said Conti, Valerie; Vella, Norbert; Saliba, Christian; Said, Edith; Ellul, Bridget; Grima, David; Felice, Alex E.
2005Comparative frequency of Coagulation Factor II and Coagulation Factor V Alleles among new-born and senior citizensAbela Medici, Joseph; Bezzina Wettinger, Stephanie; Scerri, Christian; Grochowska, Alicha; Felice, Alex E.
2007Developmental 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 homozygotesPulis, Svetlana; Scerri, Christian A.; Schembri Wismayer, Pierre; Galdies, Ruth; Bezzina Wettinger, Stephanie; Felice, Alex E.
2007Environmental risk factors for Parkinson’s disease and Parkinsonism : the Geoparkinson studyDick, Finlay D.; Palma, Giuseppe de; Ahmadi, Ahmad; Scott, Neil W.; Prescott, Gordon James; Bennett, Jami; Semple, Sean; Dick, Smita; Counsell, Carl E.; Mozzoni, Paula; Haites, Neva E.; Bezzina Wettinger, Stephanie; Mutti, Antonio; Otelea, M.; Seaton, Anthony W.H.; Soderkvist, Peter; Felice, Alex E.
2007Gene-environment interactions in parkinsonism and Parkinson’s diseaseDick, Finlay D.; Palma, Giuseppe de; Ahmadi, Ahmad; Osborne, A.; Scott, Neil W.; Prescott, Gordon James; Bennett, Jami; Semple, Sean; Dick, Smita; Mozzoni, Paula; Haites, Neva E.; Bezzina Wettinger, Stephanie; Mutti, Antonio; Otelea, M.; Seaton, Anthony W. H.; Soderkvist, Peter; Felice, Alex E.
2016Genetic causes of Parkinson’s disease in the Maltese : a study of selected mutations in LRRK2, MTHFR, QDPR and SPRZahra, Charmaine; Tabone, Christine; Camilleri, Graziella; Felice, Alex E.; Farrugia, Rosienne; Bezzina Wettinger, Stephanie
2019-06Local allele frequencies of the 5-HTTLPR serotonin transporter promoter polymorphismGrech, Christopher; Bezzina Wettinger, Stephanie; Farrugia, Rosienne
2014Mendelian randomization in inflammatory conditions - the exception rather than the rule?Bezzina Wettinger, Stephanie; Doggen, C.; Spek, A.; Rosendaal, F. R.; Reitsma, P. H.; Spek, A.; Felice, Alex E.
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.
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.
2007RNA profiling and the genetics of myocardial infarctionFelice, A.E.; Reitsma, P.H.; Bezzina Wettinger, Stephanie