A novel mutation W388X underlying properdin deficiency in a Finnish family

Por Helminen, Merja, Seitsonen, Sanna, Jarva, Hanna, Meri, Seppo, Järvelä, Irma E
Publicado em 2012

Lack of Complement Inhibitors in the Outer Intracranial Artery Aneurysm Wall Associates with Complement Terminal Pathway Activation

Por Tulamo, Riikka, Frösen, Juhana, Paetau, Anders, Seitsonen, Sanna, Hernesniemi, Juha, Niemelä, Mika, Järvelä, Irma, Meri, Seppo
Publicado em 2010

Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration

Por Tolppanen, Anna-Maija, Nevalainen, Tanja, Kolehmainen, Marjukka, Seitsonen, Sanna, Immonen, Ilkka, Uusitupa, Matti, Kaarniranta, Kai, Pulkkinen, Leena
Publicado em 2009

The genetic variant rs4073 A→T of the Interleukin‐8 promoter region is associated with the earlier onset of exudative age‐related macular degeneration

Por Hautamäki, Asta, Seitsonen, Sanna, Holopainen, Juha M., Moilanen, Jukka A., Kivioja, Jarno, Onkamo, Päivi, Järvelä, Irma, Immonen, Ilkka
Publicado no Acta Ophthalmol (2015)

Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein()

Por Laine, Matti, Jarva, Hanna, Seitsonen, Sanna, Haapasalo, Karita, Lehtinen, Markus J., Lindeman, Nina, Anderson, Don H., Johnson, Patrick T., Järvelä, Irma, Jokiranta, T. Sakari, Hageman, Gregory S., Immonen, Ilkka, Meri, Seppo
Publicado no J Immunol (2007)

Multifactor Effects and Evidence of Potential Interaction between Complement Factor H Y402H and LOC387715 A69S in Age-Related Macular Degeneration

Por Seitsonen, Sanna P., Onkamo, Päivi, Peng, Gang, Xiong, Momiao, Tommila, Petri V., Ranta, Päivi H., Holopainen, Juha M., Moilanen, Jukka A., Palosaari, Tapani, Kaarniranta, Kai, Meri, Seppo, Immonen, Ilkka R., Järvelä, Irma E.
Publicado em 2008