1. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome;Meretoja;Ann Clin Res,1969
2. Tautiperintöämme: suomalainen amyloiditauti (The Finnish amyloid disease representing our disease inheritage);Meretoja;J Finn Med Assoc,1976
3. Familial occurrence of a bulbar paralytic form of amyotropic lateral sclerosis with reticular corneal dystrophy and cutis hyperelastica in 3 sisters;Klaus;Psychiatr Neurol (Basel),1959
4. An hereditary syndrome consisting of peripheral polyneuropathy, skin changes and lattice-shaped corneal dystrophy;Winkelman;Klin Monatsbl Augenheilkd,1971
5. Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy;Boysen;J Neurol Neurosurg Psychiatry,1979