Akira Tsujino

<i>TDP</i>‐<i>43</i> mutation in familial amyotrophic lateral sclerosis

Akio Yokoseki, Atsushi Shiga, Chun‐Feng Tan et al. · Annals of Neurology · 2008 · 368 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Mendelian Disorder +13

Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome

Kazuhiko Arima, Akira Kinoshita, Hiroyuki Mishima et al. · Proceedings of the National Academy of Sciences · 2011 · 317 citations · Full text

Autoinflammatory Disorder, Immunology, Proteasome +29

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation

Chun‐Feng Tan, Hiroto Eguchi, Asako Tagawa et al. · Acta Neuropathologica · 2007 · 292 citations

Neuronal Inclusions, Amyotrophic Lateral Sclerosis, Neurological Disorder +8

Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans

Kinji Ohno, Akira Tsujino, Joan M. Brengman et al. · Proceedings of the National Academy of Sciences · 2001 · 263 citations · Full text

Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme

Kinji Ohno, Joan M. Brengman, Akira Tsujino et al. · Proceedings of the National Academy of Sciences · 1998 · 249 citations · Full text

Collagenic Tail, Genetics, Molecular Biology +16