Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Puomila A"'
Publikováno v:
In Molecular Genetics and Metabolism 2007 90(3):298-306
Autor:
Puomila, Iida
The movement towards developing existing education systems to be more inclusive can be seen worldwide. However, even in a country such as Finland where inclusive ideology has been promoted in national policies for a considerable time, there are exist
Externí odkaz:
http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-44177
Autor:
Puomila, Anu *, Viitanen, Tommi, Savontaus, Marja-Liisa, Nikoskelainen, Eeva, Huoponen, Kirsi
Publikováno v:
In Journal of the Neurological Sciences 2002 205(1):41-45
Autor:
Puomila, Heini
Ratsastus on suomalaisten lasten keskuudessa suosittu harrastus, jonka alkuvaiheet vietetään usein ratsastuskouluissa. Ratsastuksenopettajat ovat pedagogisen koulutuksen saaneita alansa ammattilaisia, mutta kasvatuksen voidaan katsoa jääneen heid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4853::b58e7520a8b790cbe9967536d145058b
https://trepo.tuni.fi/handle/10024/103468
https://trepo.tuni.fi/handle/10024/103468
Autor:
Puomila, Anu1,2 anu.puomila@utu.fi, Hämäläinen, Petra1, Kivioja, Sanna1, Savontaus, Marja-Liisa1, Koivumäki, Satu3, Huoponen, Kirsi1, Nikoskelainen, Eeva4
Publikováno v:
European Journal of Human Genetics. Oct2007, Vol. 15 Issue 10, p1079-1089. 11p. 1 Diagram, 5 Charts.
Autor:
Puomila, Anu1,2 anu.puomila@utu.fi, Huoponen, Kirsi1, Mäntyjärvi, Maija3, Hämäläinen, Petra1, Paananen, Reetta1, Sankila, Eeva-Marja4, Savontaus, Marja-Liisa1, Somer, Mirja5, Nikoskelainen, Eeva3
Publikováno v:
Acta Ophthalmologica Scandinavica. Jun2005, Vol. 83 Issue 3, p337-346. 10p.
Autor:
Huoponen, Kirsi1,2, Puomila, Anu1,2, Savontaus, Marja-Liisa1,2, Mustonen, Eila3, Kronqvist, Elina4, Nikoskelainen, Eeva5
Publikováno v:
Acta Ophthalmologica Scandinavica. Feb2002, Vol. 80 Issue 1, p38-43. 6p.
Autor:
Petra Hämäläinen, Kirsi Huoponen, Eeva Nikoskelainen, Sanna Kivioja, Anu Puomila, Satu Koivumäki, Marja-Liisa Savontaus
Publikováno v:
European Journal of Human Genetics. 15:1079-1089
We have performed an entire-population-based survey of the epidemiology and penetrance of Leber hereditary optic neuropathy (LHON) in Finland - a country that is among the best-studied genetic isolates in the world. During our long-term clinical foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62318f9b06c17c37768c8fb3650bd6fd
https://doi.org/10.1038/sj.ejhg.5201828
https://doi.org/10.1038/sj.ejhg.5201828
Publikováno v:
Molecular Genetics and Metabolism. 90(3):298-306
The human SLC7A7 gene encodes y(+)L amino acid transporter-1 (y(+)LAT-1). Mutations in the SLC7A7 coding region cause a rare recessive disorder, lysinuric protein intolerance (LPI). LPI is enriched in the Finnish population, where all patients carry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00da989f9fec14c0ce0f2016ed905c8f
https://doi.org/10.1016/j.ymgme.2006.11.007
https://doi.org/10.1016/j.ymgme.2006.11.007