[Pj-038] Motor Neuron Disease (Cognition and pathophysiology)

[Pj-038-7] Clinico-pathological features of familial amyotrophic lateral sclerosis with a SOD1 L126S mutation

^○Tomoyasu Matsubara¹, Masaya Oda², Hijiri Ito², Takashi Kurashige³, Chigusa Watanabe⁴, Yoshiro Tachiyama⁵, Toshitaka Kawarai⁶, Miyamoto Ryosuke⁶, Yokota Osamu⁷, Takashi Haraguchi⁸, Seishi Terada⁹, Shigeo Murayama¹, Izumi Yuishin^2,6 (1.Department of Neurology and Neuropathology (Brain Bank for Aging Research), Tokyo Metropolitan Geriatric Hospital & Institute of Gerontology, Tokyo, Japan, 2.Department of Neurology, Mifukai Vihara Hananosato Hospital, Hiroshima, Japan, 3.Department of Neurology, National Hospital Organization Kure Medical Center, Hiroshima, Japan, 4.Department of Neurology, National Hospital Organization Hiroshima-Nishi Medical Center, Hiroshima, Japan, 5.Department of Pathology and Laboratory Medicine, National Hospital Organization Hiroshima-Nishi Medical Center, Hiroshima, Japan, 6.Department of Clinical Neuroscience, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan, 7.Department of Psychiatry, Kinoko Espoir Hospital, Okayama, Japan, 8.Department of Neurology, National Hospital Organization Minami-Okayama Medical Center, Okayama, Japan, 9.Department of Neuropsychiatry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan)