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Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid

by Mao, Qinwen , Wu, Jane Y. , Mesulam, Marsel , Bigio, Eileen H. , Siddique, Nailah , Geula, Changiz , Siddique, Teepu , Bit-Ivan, Esther N. , Ganti, Rakhee , Deng, Han-Xiang , Peterson, Melanie

in Alzheimer's disease / Amyloid - metabolism / Amyotrophic lateral sclerosis / Amyotrophic Lateral Sclerosis - pathology / Basophils - pathology / Basophils - ultrastructure / Correspondence / DNA-Binding Proteins - metabolism / Frontotemporal Lobar Degeneration - pathology / Humans / Inclusion Bodies - pathology / Inclusion Bodies - ultrastructure / Localization / Medicine / Medicine & Public Health / Microscopy / Motor Cortex - metabolism / Motor Cortex - pathology / Motor Cortex - ultrastructure / Mutation / Neurons / Neurosciences / Pathology / Potassium / RNA-Binding Protein FUS - metabolism

2013

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by Mao, Qinwen , Wu, Jane Y. , Mesulam, Marsel , Bigio, Eileen H. , Siddique, Nailah , Geula, Changiz , Siddique, Teepu , Bit-Ivan, Esther N. , Ganti, Rakhee , Deng, Han-Xiang , Peterson, Melanie

2013

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by Mao, Qinwen , Wu, Jane Y. , Mesulam, Marsel , Bigio, Eileen H. , Siddique, Nailah , Geula, Changiz , Siddique, Teepu , Bit-Ivan, Esther N. , Ganti, Rakhee , Deng, Han-Xiang , Peterson, Melanie

2013

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