Browsing by Author Farrugia, Rosienne

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 7 of 7
Issue DateTitleAuthor(s)
2018-12Analysing the building blocks : gene sequencing for disease treatmentFarrugia, Rosienne
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.
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
2007Molecular genetics of tetrahydrobiopterin (BH4) deficiency in the Maltese populationFarrugia, Rosienne; Scerri, Christian A.; Attard Montalto, Simon; Parascandolo, Raymond; Neville, Brian G. R.; Felice, Alex E.
2015A novel mutation in LRRK2 influences risk for Parkinson disease in the Maltese populationCamilleri, G; Bezzina Wettinger, S; Farrugia, Rosienne; Camilleri, Simon
2005Sepiapterin reductase deficiency : a congenital dopa-responsive motor and cognitive disorderParascandolo, Raymond; Farrugia, Rosienne; Felice, Alex E.; Neville, B. G. R.