Browsing by Subject Rare diseases -- Diagnosis
Showing results 1 to 7 of 7
| Issue Date | Title | Author(s) |
| 2018-10 | Access to orphan drugs and quality of life in rare disease | Abbas, Amar; Vella Szijj, Janis; Serracino-Inglott, Anthony |
| 2006 | Griscelli syndrome : a rare neonatal syndrome | Ellul, Marthese; Calvagna, Victor |
| 2021 | GYNOCARE update : modern strategies to improve diagnosis and treatment of rare gynecologic tumors - current challenges and future directions | Di Fiore, Riccardo; Suleiman, Sherif; Ellul, Bridget; O’Toole, Sharon A.; Savona-Ventura, Charles; Felix, Ana; Napolioni, Valerio; Conlon, Neil T.; Erson-Bensan, Ayse Elif; Kahramanoglu, Ilker; Azzopardi, Miriam J.; Dalmas, Miriam; Calleja, Neville; Brincat, Mark R.; Muscat-Baron, Yves; Sabol, Maja; Dimitrievska, Vera; Yordanov, Angel; Vasileva-Slaveva, Mariela; Von Brockdorff, Kristelle; Micallef, Rachel A.; Kubelac, Paul; Achimas-Cadariu, Patriciu; Vlad, Catalin; Tzortzatou, Olga; Poka, Robert; Giordano, Antonio; Felice, Alex; Reed, Nicholas; Herrington, C. Simon; Faraggi, David; Calleja-Agius, Jean |
| 2018-09 | The impact of rare diseases on health related quality of life | Abbas, Amar; Vella Szijj, Janis; Serracino-Inglott, Anthony |
| 2014 | Laryngeal lymphoma : the high and low grades of rare lymphoma involvement sites | Azzopardi, Charles Paul; Degaetano, James; Betts, Alexandra; Farrugia, Eric; Magri, Claude; Refalo, Nicholas; Gatt, Alexander; Camilleri, David J. |
| 2019 | Living with a rare disease | Axiak, Clayton John |
| 2018 | Rare diseases : why bother? | Agius, Francis |
