English Poster Session

[Pe-067] Parkinsonism and Related disorders (Genetics)

Sat. May 25, 2019 1:15 PM - 2:30 PM Poster Exhibition (Osaka International Convention Center 3F Event Hall)

Chair:Yaeko Ichikawa(Department of Neurology, Kyorin University) Commentator:Manabu Funayama(Research Institute of Disease of Old Age, Graduate School of Medicine, Juntendo University)

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[Pe-067-1] Reverse phenotyping of 64 cases of genetically confirmed combined/complex dystonia

Toshitaka Kawarai¹, Ryosuke Miyamoto¹, Takashi Sakamoto², Yuishin Izumi¹, Ryuji Kaji^1,3 (1.Department of Clinical Neuroscience, Institute of Biomedical Sciences, Tokushima University Graduate School, Japan, 2.Department of Neurology, National Center Hospital, NCNP, 3.National Hospital of Utano, National Hospital Organization)

[Pe-067-2] Whole exome sequencing in a young-onset dystonia in Korean: What do we learn?

Jinyoung Youn¹, Jong Kyu Park³, Ah Reum Kim², Jong Hyeon Ahn¹, Nayoung Kd. Kim², Woong-yang Park², Ji Sun Kim¹, Jin Whan Cho¹ (1.Samsung Medical Center, Sungkyunkwan University School of Medicine, Korea, 2.Samsung Genome Institute, Samsung Medical Center, Korea, 3.Soonchunhyang University Gumi Hospital, Korea)

[Pe-067-3] Comprehensive study of LRRK2 mutations in familial Parkinson's disease in Japan

Hiroyo Yoshino¹, Aya Ikeda², Yuanzhe Li², Manabu Funayama^1,2,3, Kenya Nishioka², Nobutaka Hattori^1,2,3 (1.Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Japan, 2.Department of Neurology, Juntendo University School of Medicine, 3.Laboratory of Genomic Medicine, Center for Genomic and Regenerative Medicine, Graduate School of Medicine, Juntendo University)

[Pe-067-4] Nigral degeneration without pathological protein aggregations in genetic Parkinson's diseases

Masashi Takanashi¹, Nobutaka Hattori² (1.Department of Neurology Juntendo Koshigaya Hospital, Japan, 2.Departent of Neurology Juntendo University School of Medicine)

[Pe-067-5] Clinicogenetic study on mono-allelic and bi-allelic mutation of PLA2G6 in Parkinson's disease

Manabu Funayama^1,2,3, Hiroyo Yoshino¹, Yuanzhe Li³, Yasushi Shimo³, Kenya Nishioka³, Nobutaka Hattori^1,2,3 (1.Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Japan, 2.Laboratory of Genomic Medicine, Center for genomic and Regenerative Medicine, Graduate School of Medicine, Juntendo University, Japan, 3.Department of Neurology, Juntendo University School of Medicine, Japan)

[Pe-067-6] Genotype-phenotype correlation of LRP10 mutations among familial Parkinson's disease

Kensuke Daida¹, Yuanzhe Li², Manabu Funayama², Kotaro Ogaki¹, Hiroyo Yoshino², Akio Kikuchi³, Takafumi Hasegawa³, Kenya Nishioka¹, Nobutaka Hattori^1,2 (1.Department of Neurology, Juntendo University School of Medicine, Japan, 2.Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, 3.Division of Neurology, Department of Neuroscience & Sensory Organs, Tohoku University Graduate School of Medicine)