Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jouko Meretoja"'
Autor:
Jouko Meretoja, Lyly Teppo
Publikováno v:
Acta Pathologica Microbiologica Scandinavica Section A Pathology. :432-440
A report is given of the histopathological findings in three cases of familial amyloidosis syndrome, presenting neurological and other symptoms, of which progressive facial nerve paralysis and lattice dystrophy of the cornea predominated. The patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72795fe53b0529ac505db3d9feb2cf61
https://doi.org/10.1111/j.1699-0463.1971.tb01841.x
https://doi.org/10.1111/j.1699-0463.1971.tb01841.x
Autor:
Jouko Meretoja
Publikováno v:
Acta Ophthalmologica. 53:77-82
Three brothers are presented with bilateral asteroid hyalitis. The condition was mild in one vitreous, and hence a weak penetrance is suggested. This is the fourth report of familial cases, and thus an inherited aetiology in asteroid hyalitis is emph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a692157322edfadf9253e30ac2f36edd
https://doi.org/10.1111/j.1755-3768.1975.tb01140.x
https://doi.org/10.1111/j.1755-3768.1975.tb01140.x
Autor:
Jouko Meretoja, Ivan Fernandez-Madrid, Blas Frangione, Efrat Levy, Olli Koivunen, M.D. Matti Haltia
Publikováno v:
American Journal of Medical Genetics. 42:357-359
Familial amyloidosis, Finnish (FAF), is an autosomal dominant form of systemic amyloidosis with lattice corneal dystrophy and progressive cranial neuropathy as principal clinical manifestations. We have shown that the novel amyloid fibril protein fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::010426ce19e619701212ccf4a3154d44
https://doi.org/10.1002/ajmg.1320420321
https://doi.org/10.1002/ajmg.1320420321
Autor:
Jouko Meretoja
Publikováno v:
Ophthalmic Research. 19:245-254
Corneal endothelial snowflake dystrophy was diagnosed in a child of 12 years as part of an inherited syndrome associated with various oculocutaneous pigmentation disturbances and malabsorption. Altoge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5961d4f42297f0871edfbc7a7702a05
https://doi.org/10.1159/000265502
https://doi.org/10.1159/000265502
Autor:
Monique S. Roy, J. Satorre, C.G. García-Alix, G. H. M. Van Lith, B.C.P. Polak, Takaya Sasaki, A. Cardesa, M. Leys, H. Walther, H.-R. Böhme, S. Brüggemann, M. Quintana, Carl P. Herbort, Michael Blumenthal, H. Schüler, H. Stark, Fabian A. Abraham, L. Gekas, Jouko Meretoja, D. Feretis, S. Merin, Michel Matter, E. Michalopoulos, Shigeo Tsukahara, P. Scurtis, N. Brand
Publikováno v:
Ophthalmologica. 191:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccdcbb204cd96a910aba072131a91b0e
https://doi.org/10.1159/000309602
https://doi.org/10.1159/000309602
Publikováno v:
International journal of oral surgery. 5(4)
A 36-year-old woman was examined and treated for a rare odontogenic tumor in the mandible, the calcifying epithelial odontogenic tumor (CEOT), also known as the Pindborg tumor. The tumor extended from the left mandibular molar region to the right pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::488adbbb3538271db4e54861a161f5b7
https://pubmed.ncbi.nlm.nih.gov/821872
https://pubmed.ncbi.nlm.nih.gov/821872
Autor:
Jouko Meretoja
Publikováno v:
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde. 191(4)
A new type of corneal dystrophy with various oculocutaneous symptoms and other signs is described. Snowflake dystrophy is characterized by hundreds of small, round, oval or cork-screw-like white opacities in the endothelium and Descemet's membrane. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cc3e5344128bee01cd85b511a64f321
https://pubmed.ncbi.nlm.nih.gov/3878958
https://pubmed.ncbi.nlm.nih.gov/3878958
Autor:
Jouko Meretoja
Publikováno v:
Clinical genetics. 4(3)
A genetic analysis of familial systemic amyloidosis with lattice corneal dystrophy, facial paresis and nephropathy has been made. The 228 sibships which were at risk of the disease contained 851 sibs who were subdivided as follows: 207 affected, 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1441b0533d6fafb72f137e4b2d841a9d
https://pubmed.ncbi.nlm.nih.gov/4543600
https://pubmed.ncbi.nlm.nih.gov/4543600