Browsing by Author Parascandalo, Raymond
Showing results 1 to 10 of 10
| Issue Date | Title | Author(s) |
| 2016 | Aortic stenting for neonatal coarctation of the aorta : when should this be considered? | Bugeja, Justine; Cutajar, D.; Zahra, C.; Parascandalo, Raymond; Grech, Victor E.; De Giovanni, Joseph V. |
| 1987 | Evaluation of suspected coeliac disease in Maltese children, 1983-1986 | Lenicker, Herbert Manfred; Parascandalo, Raymond; Camilleri, Michael |
| 1992 | Febrile convulsions | Parascandalo, Raymond |
| 2007 | Molecular genetics of tetrahydrobiopterin (BH4) deficiency in the Maltese population | Farrugia, Rosienne; Scerri, Christian A.; Attard Montalto, Simon; Parascandalo, Raymond; Neville, Brian G. R.; Felice, Alex |
| 2013 | Overview of the blood transfusion policy in preterms on the Neonatal Intensive Care Unit | Said Conti, Valerie; Azzopardi, Eugenio; Parascandalo, Raymond; Soler, Paul; Attard Montalto, Simon |
| 1997 | Pentalogy of Cantrell : the first Maltese case with successful outcome | Grech, Victor E.; Parascandalo, Raymond; Rees, Philip G. |
| 1996 | Screening for congenital hypothyroidism in Maltese newborns using cord blood | Parascandalo, Raymond; Felice, Alex; Rizzo, M.; Vassallo Agius, Paul |
| 2005 | Sepiapterin reductase deficiency : a congenital dopa-responsive motor and cognitive disorder | Parascandalo, Raymond; Farrugia, Rosienne; Felice, Alex; Neville, Brian G. R. |
| 2012 | Sepiapterin reductase deficiency : a treatable mimic of cerebral palsy | Friedman, Jennifer; Roze, Emmanuel; Abdenur, Jose E.; Chang, Richard; Gasperini, Serena; Saletti, Veronica; Wali, Gurusidheshwar M.; Eiroa, Hernan; Neville, Brian G. R.; Felice, Alex; 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, Bwee Tien; Sykut-Cegielska, Jolanta; Szymanska, Krystyna; Thony, Beat; Blau, Nenad |
| 2019 | Two novel GJA1 variants in oculodentodigital dysplasia | Pace, Nikolai Paul; Benoit, Valerie; Agius, David; Grima, Maria Angela; Parascandalo, Raymond; Hilbert, Pascale; Borg, Isabella |
