Subtle neuropsychiatric and neurocognitive changes in hereditary gelsolin amyloidosis (AGel amyloidosis)

por Kantanen, Mari, Kiuru-Enari, Sari, Salonen, Oili, Kaipainen, Markku, Hokkanen, Laura
Publicado 2014

Hearing problems in patients with hereditary gelsolin amyloidosis

por Mustonen, Tuuli, Sivonen, Ville, Atula, Sari, Kiuru-Enari, Sari, Sinkkonen, Saku T.
Publicado 2021

Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study

por Schmidt, Eeva-Kaisa, Mustonen, Tuuli, Kiuru-Enari, Sari, Kivelä, Tero T., Atula, Sari
Publicado 2020

Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases

por Yamanaka, Shuichiro, Miyazaki, Yoichi, Kasai, Kenji, Ikeda, Shu-ichi, Kiuru-Enari, Sari, Hosoya, Tatsuo
Publicado 2013

CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease

por Auranen, Mari, Ylikallio, Emil, Shcherbii, Maria, Paetau, Anders, Kiuru-Enari, Sari, Toppila, Jussi P., Tyynismaa, Henna
Publicado 2015