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Mutations in CHCHD2 cause α-synuclein aggregation.
Ikeda A, Nishioka K, Meng H, Takanashi M, Hasegawa I, Inoshita T, Shiba-Fukushima K, Li Y, Yoshino H, Mori A, Okuzumi A, Yamaguchi A, Nonaka R, Izawa N, Ishikawa KI, Saiki H, Morita M, Hasegawa M, Hasegawa K, Elahi M, Funayama M, Okano H, Akamatsu W, Imai Y, Hattori N. Ikeda A, et al. Among authors: morita m. Hum Mol Genet. 2019 Dec 1;28(23):3895-3911. doi: 10.1093/hmg/ddz241. Hum Mol Genet. 2019. PMID: 31600778
The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1.
Hayashida A, Li Y, Yoshino H, Daida K, Ikeda A, Ogaki K, Fuse A, Mori A, Takanashi M, Nakahara T, Yoritaka A, Tomizawa Y, Furukawa Y, Kanai K, Nakayama Y, Ito H, Ogino M, Hattori Y, Hattori T, Ichinose Y, Takiyama Y, Saito T, Kimura T, Aizawa H, Shoji H, Mizuno Y, Matsushita T, Sato M, Sekijima Y, Morita M, Iwasaki A, Kusaka H, Tada M, Tanaka F, Sakiyama Y, Fujimoto T, Nagara Y, Kashihara K, Todo H, Nakao K, Tsuruta K, Yoshikawa M, Hara H, Yokote H, Murase N, Nakamagoe K, Tamaoka A, Takamiya M, Morimoto N, Nokura K, Kako T, Funayama M, Nishioka K, Hattori N. Hayashida A, et al. Among authors: morita m. Neurobiol Aging. 2021 Jan;97:146.e1-146.e13. doi: 10.1016/j.neurobiolaging.2020.06.017. Epub 2020 Jul 2. Neurobiol Aging. 2021. PMID: 32713623
Cardiovascular dysautonomia in de novo Parkinson's disease.
Oka H, Mochio S, Onouchi K, Morita M, Yoshioka M, Inoue K. Oka H, et al. Among authors: morita m. J Neurol Sci. 2006 Feb 15;241(1-2):59-65. doi: 10.1016/j.jns.2005.10.014. Epub 2005 Dec 2. J Neurol Sci. 2006. PMID: 16325862 Retracted.
[Sudomotor dysfunction in Parkinson's disease].
Yoshioka M, Oka H, Morita M, Inoue K. Yoshioka M, et al. Among authors: morita m. Rinsho Shinkeigaku. 2003 Jul;43(7):379-84. Rinsho Shinkeigaku. 2003. PMID: 14582362 Japanese.
3,509 results