Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tapani Palosaari"'
Autor:
Sanna P Seitsonen, Päivi Onkamo, Gang Peng, Momiao Xiong, Petri V Tommila, Päivi H Ranta, Juha M Holopainen, Jukka A Moilanen, Tapani Palosaari, Kai Kaarniranta, Seppo Meri, Ilkka R Immonen, Irma E Järvelä
Publikováno v:
PLoS ONE, Vol 3, Iss 12, p e3833 (2008)
Variants in the complement cascade genes and the LOC387715/HTRA1, have been widely reported to associate with age-related macular degeneration (AMD), the most common cause of visual impairment in industrialized countries.We investigated the associati
Externí odkaz:
https://doaj.org/article/69ec58c61a3746408eebad5f8d490d26
Autor:
Laura Lähteenoja, Sanna Häkli, Sari Tuupanen, Outi Kuismin, Tapani Palosaari, Elisa Rahikkala, Aura Falck
Publikováno v:
Ophthalmic Genetics. 43:152-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bcc68d6e2233736ed0689cf6c7a8df5
https://doi.org/10.1080/13816810.2022.2045511
https://doi.org/10.1080/13816810.2022.2045511
Publikováno v:
Retinal casesbrief reports. 13(1)
PURPOSE To highlight the course of blood-brain barrier disruption maculopathy in a patient with successfully managed relapsed central nervous system lymphoma. METHODS Case report with fundus autofluorescence and optical coherence tomography imaging,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb131e15080cbe45b8bb177cfd1a68bd
https://pubmed.ncbi.nlm.nih.gov/28098709
https://pubmed.ncbi.nlm.nih.gov/28098709
Publikováno v:
Acta ophthalmologica. 93(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d51ac754c96a1224b0dab534836e25c
https://pubmed.ncbi.nlm.nih.gov/25585971
https://pubmed.ncbi.nlm.nih.gov/25585971
Publikováno v:
Acta ophthalmologica. 86(7)
Purpose: To evaluate the effect of photodynamic therapy (PDT) with verteporfin on symptomatic, aggressive retinal astrocytomas. Methods: A prospective, interventional study in a tertiary referral centre. Two patients were treated with a single sessio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f057ff0ace4abb2ca6e117a36e1c0c01
https://pubmed.ncbi.nlm.nih.gov/18759802
https://pubmed.ncbi.nlm.nih.gov/18759802
Autor:
Momiao Xiong, Tapani Palosaari, Juha M. Holopainen, Päivi Onkamo, Irma Järvelä, Jukka A O Moilanen, Päivi Ranta, Petri Tommila, Ilkka Immonen, Seppo Meri, Kai Kaarniranta, Sanna Seitsonen, Gang Peng
Publikováno v:
PLoS ONE, Vol 3, Iss 12, p e3833 (2008)
PLoS ONE
PLoS ONE
Background Variants in the complement cascade genes and the LOC387715/HTRA1, have been widely reported to associate with age-related macular degeneration (AMD), the most common cause of visual impairment in industrialized countries. Methods/Principal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37efc3ffeced848c7234aa8d7fc6ddf5
http://europepmc.org/articles/PMC2585793?pdf=render
http://europepmc.org/articles/PMC2585793?pdf=render
Autor:
Seitsonen, Sanna P., Susanna Lemmelä, Juha Holopainen, Petri Tommila, Päivi Ranta, Antti Kotamies, Jukka Moilanen, Tapani Palosaari, Kai Kaarniranta, Seppo Meri, Ilkka Immonen, Irma Järvelä
Publikováno v:
Scopus-Elsevier
University of Helsinki
University of Helsinki
A strong association of a Tyr402His polymorphism in the complement factor H (CFH) gene and a Met299Val polymorphism in the elongation of very long chain fatty acids-like 4 (ELOVL4) gene with age-related macular degeneration (AMD) has been identified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3cfe9f806e3349bfe6813609b9d02780
https://pubmed.ncbi.nlm.nih.gov/16885922
https://pubmed.ncbi.nlm.nih.gov/16885922
Autor:
Tapani, Palosaari
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 121(14)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::339a7de3b41266fd3f6e801dbe838d24
https://pubmed.ncbi.nlm.nih.gov/16209315
https://pubmed.ncbi.nlm.nih.gov/16209315