Publications by authors named "Masayoshi Tada"

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L-arginine in patients with spinocerebellar ataxia type 6: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial.
Tomohiko Ishihara, Masayoshi Tada, Yoshitomi Kanemitsu, Yuji Takahashi, Kinya Ishikawa

EClinicalMedicine· December 2024

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Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping task.
Shin-Ichi Tokushige, Shunichi Matsuda, Masayoshi Tada, Ichiro Yabe, Atsushi Takeda

Clin Neurophysiol· February 2024

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[Reversible Cerebral Vasoconstriction Syndrome(RCVS)and Posterior Reversible Encephalopathy Syndrome(PRES)].
Masayoshi Tada

No Shinkei Geka· March 2021

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Arginine is a disease modifier for polyQ disease models that stabilizes polyQ protein conformation.
Eiko N Minakawa, Helena Akiko Popiel, Masayoshi Tada, Toshiaki Takahashi, Hiroshi Yamane

Brain· June 2020

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Role of RNF213 p.4810K variant in the development of intracranial arterial disease in patients treated with nilotinib.
Masahiro Uemura, Masato Kanazawa, Takuma Yamagishi, Takahiro Nagai, Mami Takahashi, Masayoshi Tada

J Neurol Sci· January 2020

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Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Hiroyuki Ishiura, Koichiro Doi, Jun Mitsui, Jun Yoshimura, Miho Kawabe Matsukawa, Masayoshi Tada

Nat Genet· April 2018

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[Overview of Hereditary Spinocerebellar Ataxias in Japan].
Masayoshi Tada, Akio Yokoseki, Osamu Onodera

Brain Nerve· August 2017

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Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids.
Mari Tada, Takuya Konno, Masayoshi Tada, Toshiyuki Tezuka, Takeshi Miura

Ann Neurol· October 2016

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Roles of inositol 1,4,5-trisphosphate receptors in spinocerebellar ataxias.
Masayoshi Tada, Masatoyo Nishizawa, Osamu Onodera

Neurochem Int· March 2016

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Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems.
Masayoshi Tada, Masatoyo Nishizawa, Osamu Onodera

J Neurol Neurosurg Psychiatry· August 2015

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[Disease notification and self-determination in treatment decisions for patients with Creutzfeldt-Jakob disease].
Fumihiro Yanagimura, Takayoshi Shimohata, Masayoshi Tada, Hiroaki Nozaki, Masatoyo Nishizawa

Rinsho Shinkeigaku· April 2015

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A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.
Gen Tamiya, Satoshi Makino, Makiko Hayashi, Akiko Abe, Chikahiko Numakura, Masayoshi Tada

Am J Hum Genet· September 2014

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Progressive myoclonus epilepsy: extraneuronal brown pigment deposition and system neurodegeneration in the brains of Japanese patients with novel SCARB2 mutations.
Yong-Juan Fu, Izumi Aida, Masayoshi Tada, Mari Tada, Yasuko Toyoshima

Neuropathol Appl Neurobiol· August 2014

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[Hereditary diffuse leukoencephalopathy with spheroids (HDLS): a review of the literature on its clinical characteristics and mutations in the colony-stimulating factor-1 receptor gene].
Takuya Konno, Masayoshi Tada, Mari Tada, Masatoyo Nishizawa, Takeshi Ikeuchi

Brain Nerve· May 2014

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Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS.
Takuya Konno, Masayoshi Tada, Mari Tada, Akihide Koyama, Hiroaki Nozaki

Neurology· January 2014

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Coexistence of Huntington's disease and amyotrophic lateral sclerosis: a clinicopathologic study.
Mari Tada, Elizabeth A Coon, Alexander P Osmand, Patricia A Kirby, Wayne Martin, Masayoshi Tada

Acta Neuropathol· November 2012

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Early adult-onset orbital apex Langerhans cell histiocytosis histologically confirmed during "truly spontaneous" regression.
Keisuke Satoh, Masayoshi Tada, Hiroshi Shimizu, Yuichiro Yoneoka

Acta Neurochir (Wien)· February 2012

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Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.
Akio Yokoseki, Tomohiko Ishihara, Akihide Koyama, Atsushi Shiga, Mitsunori Yamada, Masayoshi Tada

Brain· May 2011

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Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.
Masayoshi Tada, Akio Yokoseki, Tatsuya Sato, Takao Makifuchi, Osamu Onodera

Adv Exp Med Biol· August 2010

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Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
Giovanni Stevanin, Hamid Azzedine, Paola Denora, Amir Boukhris, Meriem Tazir, Masayoshi Tada

Brain· March 2008

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Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends.
Tetsuya Takahashi, Masayoshi Tada, Shuichi Igarashi, Akihide Koyama, Hidetoshi Date

Nucleic Acids Res· July 2007

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Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy.
Mari Tada, Osamu Onodera, Masayoshi Tada, Tetsutaro Ozawa, Yue-Shan Piao

Arch Neurol· February 2007

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Long-term therapeutic efficacy and safety of low-dose tacrolimus (FK506) for myasthenia gravis.
Masayoshi Tada, Takayoshi Shimohata, Mari Tada, Mutsuo Oyake, Shuichi Igarashi

J Neurol Sci· August 2006

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[Oral cyclophosphamide therapy for multifocal fibrosclerosis with hypertrophic intracranial pachymeningitis].
Masayoshi Tada, Osamu Onodera, Kenju Hara, Keiko Tanaka, Hitoshi Takahashi

Rinsho Shinkeigaku· February 2006

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Babinski-Nageotte syndrome with ipsilateral hemiparesis.
Masayoshi Tada, Mari Tada, Hideaki Ishiguro, Kouichi Hirota

Arch Neurol· April 2005

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