• A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish type
• Amyloid in parenchymal organs in gelsolin (AGel) amyloidosis
• Association between first language and SARS-CoV-2 infection rates, hospitalization, intensive care admissions and death in Finland: a population-based observational cohort study
• Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
• Clinical and genetical diagnosis of a case of Meretoja syndrome and frontotemporal lifting procedure
• Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel <em>GSN</em> Variant p.Glu580Lys
• Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation
• Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families
• Contact lens induced bacterial keratitis in LCD II: Management and multimodal imaging: a case report and review of literature
• Deep Learning Algorithms for Corneal Amyloid Deposition Quantitation in Familial Amyloidosis
• Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study
• Health sector spending and spending on HIV/AIDS, tuberculosis, and malaria, and development assistance for health: progress towards Sustainable Development Goal 3
• Lattice Corneal Dystrophy
• Lattice Corneal Dystrophy
• Mapping age- and sex-specific HIV prevalence in adults in sub-Saharan Africa, 2000-2018
• Mapping local patterns of childhood overweight and wasting in low- and middle-income countries between 2000 and 2017
• Meretoja Syndrome: General Considerations and Contributions of Plastic Surgery in Surgical Treatment
• Myocardial tissue characterization in patients with hereditary gelsolin (AGel) amyloidosis using novel cardiovascular magnetic resonance techniques
• Nanobody interaction unveils structure, dynamics and proteotoxicity of the Finnish-type amyloidogenic gelsolin variant
• Selective and Sensitive Pull Down of Amyloid Fibrils Produced in Vitro and in Vivo by the Use of Pentameric-Thiophene-Coupled Resins
• Severe ocular involvement in hereditary gelsolin amyloidosis
• Systemic diseases and the cornea
• The role of gelsolin domain 3 in familial amyloidosis (Finnish type)