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We report a case of glial mixed tau and <jats:styled-content style=\"fixed-case\">TDP<\/jats:styled-content>\u201043 proteinopathies in a <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>apanese patient diagnosed clinically as having <jats:styled-content style=\"fixed-case\">ALS\u2010D<\/jats:styled-content>. Autopsy revealed loss of lower motor neurons and degeneration of the pyramidal tracts in the spinal cord and brain stem. The brain showed frontotemporal lobar degeneration (<jats:styled-content style=\"fixed-case\">FTLD<\/jats:styled-content>), the most severe neuronal loss and gliosis being evident in the precentral gyrus. Although less severe, such changes were also observed in other brain regions, including the basal ganglia and substantia nigra. <jats:styled-content style=\"fixed-case\">AT<\/jats:styled-content>8 immunostaining revealed that predominant occurrence of astrocytic tau lesions termed globular astrocytic inclusions (<jats:styled-content style=\"fixed-case\">GAIs<\/jats:styled-content>) was a feature of the affected regions. These <jats:styled-content style=\"fixed-case\">GAI<\/jats:styled-content>s were <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>allyas\u2010<jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>raak negative. Neuronal and oligodendrocytic tau lesions were comparatively scarce. p<jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>409\/410 immunostaining also revealed similar neuronal and glial <jats:styled-content style=\"fixed-case\">TDP<\/jats:styled-content>\u201043 lesions. Interestingly, occasional co\u2010localization of tau and <jats:styled-content style=\"fixed-case\">TDP<\/jats:styled-content>\u201043 was evident in the <jats:styled-content style=\"fixed-case\">GAI<\/jats:styled-content>s. Immunoblot analyses revealed band patterns characteristic of a 4\u2010repeat (4<jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>) tauopathy, corticobasal degeneration and a <jats:styled-content style=\"fixed-case\">TDP<\/jats:styled-content>\u201043 proteinopathy, <jats:styled-content style=\"fixed-case\">ALS\/FTLD\u2010TDP<\/jats:styled-content>\u2005<jats:italic>Type<\/jats:italic>\u2005<jats:styled-content style=\"fixed-case\"><jats:italic>B<\/jats:italic><\/jats:styled-content>. No mutations were found in the <jats:styled-content style=\"fixed-case\"><jats:italic>MAPT<\/jats:italic><\/jats:styled-content> or <jats:styled-content style=\"fixed-case\"><jats:italic>TDP<\/jats:italic><\/jats:styled-content><jats:italic>\u201043<\/jats:italic> genes. We consider that this patient harbored a distinct, sporadic globular glial mixed 4<jats:styled-content style=\"fixed-case\">R<\/jats:styled-content> tau and <jats:styled-content style=\"fixed-case\">TDP<\/jats:styled-content>\u201043 proteinopathy associated with motor neuron disease and <jats:styled-content style=\"fixed-case\">FTD<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/bpa.12262","type":"journal-article","created":{"date-parts":[[2015,3,19]],"date-time":"2015-03-19T04:43:56Z","timestamp":1426740236000},"page":"82-94","source":"Crossref","is-referenced-by-count":28,"title":["Globular Glial Mixed Four Repeat Tau and <scp>TDP<\/scp>\u201043 Proteinopathy with Motor Neuron Disease and Frontotemporal Dementia"],"prefix":"10.1111","volume":"26","author":[{"given":"Ryoko","family":"Takeuchi","sequence":"first","affiliation":[{"name":"Department of Pathology Brain Research Institute University of Niigata  Niigata Japan"},{"name":"Department of Neurology Brain Research Institute 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