FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

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作者
Robert Rusina
Gabor G Kovacs
Jindřich Fiala
Jakub Hort
Petr Ridzoň
Iva Holmerová
Thomas Ströbel
Radoslav Matěj
机构
[1] Thomayer Teaching Hospital and Institute for Postgraduate Education in Medicine,Department of Neurology
[2] Medical University of Vienna,Institute of Neurology
[3] Charles University,Department of Neurology
[4] 2nd Medical Faculty and Motol Teaching Hospital,Centre of Gerontology and Faculty of Humanity Studies
[5] International Clinical Research Center,Department of Pathology and Molecular Medicine
[6] Charles University in Prague,Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine
[7] Thomayer Teaching Hospital,undefined
[8] Charles University in Prague,undefined
来源
BMC Neurology | / 11卷
关键词
Multiple System Atrophy; Progressive Supranuclear Palsy; Motor Neuron Disease; Frontotemporal Dementia; Progressive Supranuclear Palsy;
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