1 - 7 of about 7

• 1.

  Non-lesional skin biopsy for a diagnosis of neuronal intranuclear inclusion disease , Ito Ayako, Adachi Tadashi, Yoshida Yuichi, Adachi Koji, Yamamoto Osamu , J Dermatol , vol.30 , 2017 , The Multiple Authorship , English

• 2.

  Cognitive and behavioral status in Japanese ALS patients: a multicenter study. , Watanabe Y, Raaphorst J, Izumi Y, Yoshino H, Ito S, Adachi T, Takigawa H, Masuda M, Atsuta N, Adachi Y, Isose S, Arai K, Yokota O, Oda M, Ogino M, Ichikawa H, Hasegawa K, Kimura H, Shimizu T, Aiba I, Yabe H, Kanba M, Kusumi K, Aoki T, Hiroe Y, Watanabe H, Nishiyama K, Nomoto M, Sobue G, Beeldman E, Hanajima R, Nakashima K; ALS-FTD-Q-J research group. , J Neurol. , 2020.01 , There is Review , The Multiple Authorship , English

• 3.

  A Single-institution Study on Predictors of Short-term Progression from Mild Cognitive Impairment in Parkinson's Disease to Parkinson's Disease with Dementia. , Tajiri Y, Wada-Isoe K, Tanaka K, Adachi T, Hanajima R, Nakashima K. , Yonago Acta Med. , 2020.01 , There is Review , The Multiple Authorship , English

• 4.

  Cerebral Venous Thrombosis due to Nontyphoidal Salmonella Bacteremia. , Taneda K, Adachi T, Watanabe Y, Hanajima R. , Intern Med. , vol.58 (13) (p.1943 - 1946) , 2019.07 , There is Review , The Multiple Authorship , English

• 5.

  Tau and TDP-43 accumulation of the basal nucleus of Meynert in individuals with cerebral lobar infarcts or hemorrhage. , Hatsuta H, Takao M, Nogami A, Uchino A, Sumikura H, Takata T, Morimoto S, Kanemaru K, Adachi T, Arai T, Hasegawa M, Murayama S. , Acta Neuropathol Commun. , vol.28 (7) , 2019 , There is Review , The Multiple Authorship , English

• 6.

  Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2. , Yuan JH, Hashiguchi A, Okamoto Y, Yoshimura A, Ando M, Shiomi K, Saito K, Takahashi M, Ichinose K, Ohmichi T, Ichikawa K, Tadashi A, Takigawa H, Shibayama H, Takashima H. , J Hum Genet , vol.63 (p.281 - 287) , 2018 , There is Review , The Multiple Authorship , English

• 7.

  Cowden Syndrome with a Novel PTEN Mutation Presenting with Partial Epilepsy Related to Focal CorticalDysplasia , Adachi Tadashi, Takigawa Hiroshi, , Nomura Takashi, Watanabe Yasuhiro, Kowa Hisanori , Intern Med , vol.16 , 2017 , The Multiple Authorship , English

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