Browsing Publikasjoner fra CRIStin FHI by Journals "Orphanet Journal of Rare Diseases"

Now showing items 1-2 of 2

Porphyria cutanea tarda and patterns of long-term sick leave and disability pension: a 24-year nationwide matched-cohort study

Baravelli, Carl Michael; Aarsand, Aasne Karine; Sandberg, Sverre; Tollånes, Mette Christophersen (Peer reviewed; Journal article, 2022)
Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Coi, Alessio; Santoro, Michele; Pierini, Anna; Rankin, Judith; Glinianaia, Svetlana V.; Tan, Joachim; Reid, Abigail-Kate; Garne, Ester; Loane, Maria; Given, Joanne; Ballardini, Elisa; Cavero-Carbonell, Clara; de Walle, Hermien E.K.; Gatt, Miriam; García-Villodre, Laura; Gissler, Mika; Jordan, Sue; Kiuru-Kuhlefelt, Sonja; Kjaer Urhoj, Stine; Klungsøyr, Kari; Lelong, Nathalie; Lutke, L. Renée; Neville, Amanda J.; Rahshenas, Makan; Scanlon, Ieuan; Wellesley, Diana; Morris, Joan K. (Peer reviewed; Journal article, 2022)