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Genotype-phenotype correlations of cysteine replacement in CADASIL.
Neurobiol Aging. 2017 Feb;50:169.e7-169.e14. doi: 10.1016/j.neurobiolaging.2016.10.026. Epub 2016 Nov 2.
Neurobiol Aging. 2017.
PMID: 27890607
FBXO7 mutations in Parkinson's disease and multiple system atrophy.
Conedera S, Apaydin H, Li Y, Yoshino H, Ikeda A, Matsushima T, Funayama M, Nishioka K, Hattori N.
Conedera S, et al.
Neurobiol Aging. 2016 Apr;40:192.e1-192.e5. doi: 10.1016/j.neurobiolaging.2016.01.003. Epub 2016 Jan 14.
Neurobiol Aging. 2016.
PMID: 26882974
Review.
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Genetic analysis of TMEM230 in Japanese patients with familial Parkinson's disease.
Conedera SA, Li Y, Funayama M, Yoshino H, Nishioka K, Hattori N.
Conedera SA, et al.
Parkinsonism Relat Disord. 2018 Mar;48:107-108. doi: 10.1016/j.parkreldis.2017.12.020. Epub 2017 Dec 19.
Parkinsonism Relat Disord. 2018.
PMID: 29305083
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A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease.
Ikeda A, Matsushima T, Daida K, Nakajima S, Conedera S, Li Y, Yoshino H, Oyama G, Funayama M, Nishioka K, Hattori N.
Ikeda A, et al. Among authors: conedera s.
Parkinsonism Relat Disord. 2017 Jan;34:66-68. doi: 10.1016/j.parkreldis.2016.10.018. Epub 2016 Oct 24.
Parkinsonism Relat Disord. 2017.
PMID: 28341223
No abstract available.
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