Blar i Publikasjoner fra CRIStin FHI på tidsskrift "Orphanet Journal of Rare Diseases"
Viser treff 1-2 av 2
-
Porphyria cutanea tarda and patterns of long-term sick leave and disability pension: a 24-year nationwide matched-cohort study
(Peer reviewed; Journal article, 2022) -
Survival of children with rare structural congenital anomalies: a multi-registry cohort study
(Peer reviewed; Journal article, 2022)