Objective To see whether the distribution patterns of phosphorylated 43kDa TAR DNA‐binding
protein (pTDP‐43) intraneuronal inclusions in amyotrophic lateral sclerosis (ALS) permit …

Objective: A study was undertaken to examine the neuropathological substrates of cognitive
dysfunction and dementia in Parkinson disease (PD). Methods: One hundred forty patients …

… John L Robinson , John L Robinson … Y Lee, John Q Trojanowski, Neurodegenerative
disease concomitant proteinopathies are prevalent, age-related and APOE4-associated, Brain, …

In Lewy body diseases—including Parkinson’s disease, without or with dementia, dementia
with Lewy bodies, and Alzheimer’s disease with Lewy body co-pathology 1 —α-synuclein (α-…

Progressive supranuclear palsy (PSP) is a 4R-tauopathy predominated by subcortical pathology
in neurons, astrocytes, and oligodendroglia associated with various clinical phenotypes…

We examined regional distribution patterns of phosphorylated 43-kDa TAR DNA-binding
protein (pTDP-43) intraneuronal inclusions in frontotemporal lobar degeneration (FTLD). …

We examined the phosphorylated 43-kDa TAR DNA-binding protein (pTDP-43) inclusions
as well as neuronal loss in full-length spinal cords and five selected regions of the central …

C9ORF72-hexanucleotide repeat expansions and ubiquilin-2 (UBQLN2) mutations are
recently identified genetic markers in amyotrophic lateral sclerosis (ALS) and frontotemporal …

Microglia coordinate various functions in the central nervous system ranging from removing
synaptic connections, to maintaining brain homeostasis by monitoring neuronal function, …

Neurodegenerative diseases (NDs) are defined by the accumulation of abnormal protein
deposits in the central nervous system (CNS), and only neuropathological examination …