Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Vesaluoma, Minna H"'
Autor:
Chidambaram, Jaya D., Prajna, Namperumalsamy V., Larke, Natasha L., Palepu, Srikanthi, Lanjewar, Shruti, Shah, Manisha, Elakkiya, Shanmugam, Lalitha, Prajna, Carnt, Nicole, Vesaluoma, Minna H., Mason, Melanie, Hau, Scott, Burton, Matthew J.
Publikováno v:
In Ophthalmology November 2016 123(11):2285-2293
Autor:
Moilanen, Jukka A.O *, Holopainen, Juha M, Helintö, Maaret, Vesaluoma, Minna H, Tervo, Timo M.T
Publikováno v:
In Journal of Cataract & Refractive Surgery 2004 30(2):341-349
Autor:
Tuominen, Ilpo S.J, Tervo, Timo M.T, Teppo, Anna-Maija, Valle, Tuuli U, Grönhagen-Riska, Carola, Vesaluoma, Minna H
Publikováno v:
In Experimental Eye Research June 2001 72(6):631-641
Publikováno v:
In Ophthalmology March 2000 107(3):565-573
Autor:
Vesaluoma, Minna H *, Petroll, W.Matthew, Pérez-Santonja, Juan J, Valle, Tuuli U, Alió, Jorge L, Tervo, Timo M.T
Publikováno v:
In American Journal of Ophthalmology 2000 130(5):564-573
Autor:
Kirveskari, Juha, Vesaluoma, Minna H., Moilanen, Jukka A.O., Tervo, Timo M.T., Petroll, Matthew W., Linnolahti, Eeva, Renkonen, Risto
Publikováno v:
Nature Medicine. Mar2001, Vol. 7 Issue 3, p376. 4p.
Publikováno v:
In Ophthalmology 1999 106(5):944-951
Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type)
Autor:
Rosenberg, Maria E., Tervo, Timo M. T., Gallar, Juana, Acosta, M. Carmen, Müller, Linda J., Moilanen, Jukka A. O., Tarkkanen, Ahti H. A., Vesaluoma, Minna H.
[Purpose] 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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1106::532864c88c971cb8f02520a543a2535b
http://hdl.handle.net/10261/289499
http://hdl.handle.net/10261/289499
Autor:
Vesaluoma, Minna H., Sankila, Eeva–Marja, Gallar, Juana, Müller, Linda J., Petroll, W. Matthew, Moilanen, Jukka A. O., Forsius, Henrik, Tervo, Timo M. T.
[Purpose]: 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 R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1106::575746e6ea8a3e5632b12ae381422869
http://hdl.handle.net/10261/288754
http://hdl.handle.net/10261/288754
Publikováno v:
In Journal of Cataract & Refractive Surgery 2004 30(1):253-256