Related references
Note: Only part of the references are listed.Neuropathological profile of long-duration amyotrophic lateral sclerosis in military Veterans
Keith R. Spencer et al.
BRAIN PATHOLOGY (2020)
TDP-43 induces mitochondrial damage and activates the mitochondrial unfolded protein response
Peng Wang et al.
PLOS GENETICS (2019)
Dipeptide repeat (DPR) pathology in the skeletal muscle of ALS patients with C9ORF72 repeat expansion
Matthew D. Cykowski et al.
ACTA NEUROPATHOLOGICA (2019)
Prion-Like Propagation of Protein Misfolding and Aggregation in Amyotrophic Lateral Sclerosis
Luke McAlary et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2019)
TDP-43 as a potential biomarker for amyotrophic lateral sclerosis: a systematic review and meta-analysis
Vivek Majumder et al.
BMC NEUROLOGY (2018)
Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosis
Matthew D. Cykowski et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2018)
Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS)
Leslie I. Grad et al.
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE (2017)
Clinical Significance of TDP-43 Neuropathology in Amyotrophic Lateral Sclerosis
Matthew D. Cykowski et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2017)
Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration
Edward B. Lee et al.
ACTA NEUROPATHOLOGICA (2017)
Comparative analysis of C9orf72 and sporadic disease in an ALS clinic population
Mfon E. Umoh et al.
NEUROLOGY (2016)
Axonal TDP-43 aggregates in sporadic amyotrophic lateral sclerosis
T. Onozato et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2016)
Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes
Ryoko Takeuchi et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2016)
Expanding the spectrum of neuronal pathology in multiple system atrophy
Matthew D. Cykowski et al.
BRAIN (2015)
Spread of pathology in amyotrophic lateral sclerosis: assessment of phosphorylated TDP-43 along axonal pathways
Manaal Fatima et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2015)
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
John Ravits
EXPERIMENTAL NEUROLOGY (2014)
C9ORF72-ALS: P62-AND UBIQUITIN-AGGREGATION PATHOLOGY IN SKELETAL MUSCLE
Matthias Tuerk et al.
MUSCLE & NERVE (2014)
TDP-43 pathology in the basal forebrain and hypothalamus of patients with amyotrophic lateral sclerosis
Matthew D. Cykowski et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2014)
Quantitative Analysis of Histological Staining and Fluorescence Using ImageJ
Ellen C. Jensen
ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY (2013)
Stages of pTDP-43 Pathology in Amyotrophic Lateral Sclerosis
Johannes Brettschneider et al.
ANNALS OF NEUROLOGY (2013)
Amyotrophic lateral sclerosis: a dying motor unit?
Maria Piotrkiewicz et al.
FRONTIERS IN AGING NEUROSCIENCE (2013)
Deciphering amyotrophic lateral sclerosis: What phenotype, neuropathology and genetics are telling us about pathogenesis
John Ravits et al.
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)
TDP-43 plasma levels are higher in amyotrophic lateral sclerosis
Esther Verstraete et al.
AMYOTROPHIC LATERAL SCLEROSIS (2012)
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72
Johnathan Cooper-Knock et al.
BRAIN (2012)
The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth
Claudia Fallini et al.
HUMAN MOLECULAR GENETICS (2012)
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study (vol 11, pg 232, 2012)
S. Byrne et al.
LANCET NEUROLOGY (2012)
NIH Image to ImageJ: 25 years of image analysis
Caroline A. Schneider et al.
NATURE METHODS (2012)
Loss of neurofilaments in the neuromuscular junction in a rat model of proximal axonopathy
C. Soler-Martin et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2012)
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
Susan Byrne et al.
LANCET NEUROLOGY (2012)
The Seeds of Neurodegeneration: Prion-like Spreading in ALS
Magdalini Polymenidou et al.
CELL (2011)
Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology
Yasushi Nishihira et al.
ACTA NEUROPATHOLOGICA (2009)
Clinical and Pathological Continuum of Multisystem TDP-43 Proteinopathies
Felix Geser et al.
ARCHIVES OF NEUROLOGY (2009)
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis
Felix Geser et al.
ARCHIVES OF NEUROLOGY (2008)
Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis
Koji Yamanaka et al.
NATURE NEUROSCIENCE (2008)
Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease
Nicholas J. Brandmeir et al.
ACTA NEUROPATHOLOGICA (2008)
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
Ian R. A. Mackenzie et al.
ANNALS OF NEUROLOGY (2007)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Prevalence and patterns of cognitive impairment in sporadic ALS
GM Ringholz et al.
NEUROLOGY (2005)
Share Paper
