Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mh, Vesaluoma"'
Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type)
Autor:
Me, Rosenberg, Tm, Tervo, Juana Gallar, Mc, Acosta, Lj, Müller, Ja, Moilanen, Ah, Tarkkanen, Mh, Vesaluoma
Publikováno v:
Europe PubMed Central
To describe the corneal abnormalities and to measure different modalities of corneal sensitivity in corneal lattice dystrophy type II (familial amyloidosis, Finnish type, also known as gelsolin-related amyloidosis and originally as Meretoja syndrome)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::50d90ab700fe885b34842ce1bff5265d
https://pubmed.ncbi.nlm.nih.gov/11222521
https://pubmed.ncbi.nlm.nih.gov/11222521
Autor:
Mh, Vesaluoma, Em, Sankila, Juana Gallar, Lj, Müller, Wm, Petroll, Ja, Moilanen, Forsius H, Tm, Tervo
Publikováno v:
Europe PubMed Central
Autosomal recessive corneal plana (RCP) is a rare corneal anomaly with unknown pathogenesis and a high incidence in Finland. The aim was to examine corneal sensitivity and the morphology of different corneal layers and subbasal nerves in RCP patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4142e1e490a140a28e0199601d031102
https://pubmed.ncbi.nlm.nih.gov/10892853
https://pubmed.ncbi.nlm.nih.gov/10892853