順天堂大学 · 医学研究科/医学部

研究キーワードParkinson's disease genetics・hereditary spastic paraplegia・deep brain stimulation・induced pluripotent stem cells・movement disorders・neurogenetics

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• Ishikawa K, Ishiguro M, Li Y, Nishioka K, Hattori N, Akamatsu W. Generation of three hiPSC clones from a Parkinson's disease patient with a heterozygous variant of VPS35 p.D620N. Stem Cell Research. 2022 Feb 28;60:102739.2022
• Daida K, Nishioka Y, Li Y, Yoshino H, Funayama M, Hattori N, Nishioka K. A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene. eNeurological Sci 2022 In press.2022
• Kamo H, Oyama G, Nishioka K, Funayama M, Hattori N. Deep Brain Stimulation for a Patient with Familial Parkinson’s Disease Harboring CHCHD2 p.T61I. Movement Disorders Clinical Practice. 2022 in press.2022
• Yoshino H, Li Y, Nishioka K, Daida K, Hayashida A, Ishiguro Y, Yamada D, Nana Izawa N, Nishi K, Nishikawa N, Oyama G, Hatano H, Nakamura S, Yoritaka A, Motoi Y, Funayama M, Hattori N, and the investigators of Japan Parkinson disease genetic study. Genotype-phenotype correlation of Parkinson’s disease with PRKN variants. Neurobiology of Aging. 2022 in press.2022

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