Phosphorylated TDP-43 aggregates in skeletal and cardiac muscle are a marker of myogenic degeneration in amyotrophic lateral sclerosis and various conditions

Autophagy Is a Common Degradation Pathway for Bunina Bodies and TDP-43 Inclusions in Amyotrophic Lateral Sclerosis

(2019) Fumiaki Mori et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation

(2019) Satoshi Yamashita et al.   MUSCLE & NERVE

Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosis

(2018) Matthew D. Cykowski et al.   Acta Neuropathologica Communications

TDP-43 and RNA form amyloid-like myo-granules in regenerating muscle

(2018) Thomas O. Vogler et al.   NATURE

Altered TDP-43-dependent splicing in HSPB8 -related distal hereditary motor neuropathy and myofibrillar myopathy

(2017) A. Cortese et al.   EUROPEAN JOURNAL OF NEUROLOGY

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes

(2016) Ryoko Takeuchi et al.   Acta Neuropathologica Communications

Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D

(2016) Satu Sandell et al.   Acta Neuropathologica Communications

Sporadic inclusion body myositis: clinical, pathological, and genetic analysis of eight Polish patients

(2015) Biruta Kierdaszuk et al.   FOLIA NEUROPATHOLOGICA

C9ORF72-ALS: P62- and ubiquitin-aggregation pathology in skeletal muscle

(2014) Matthias Türk et al.   MUSCLE & NERVE

Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology study

(2014) Safa Al-Sarraj et al.   Acta Neuropathologica Communications

Differential autophagy power in the spinal cord and muscle of transgenic ALS mice

(2013) Valeria Crippa et al.   Frontiers in Cellular Neuroscience

TDP-43 in skeletal muscle of patients affected with amyotrophic lateral sclerosis

(2010) Gianni Sorarú et al.   Amyotrophic Lateral Sclerosis

Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient

(2010) A. Hernandez Lain et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Enhancement of native and phosphorylated TDP-43 immunoreactivity by proteinase K treatment following autoclave heating

(2010) Fumiaki Mori et al.   NEUROPATHOLOGY

In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments

(2010) C. D'Agostino et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease

(2010) Mallikarjun Badadani et al.   PLoS One

TAR DNA-Binding Protein 43 Accumulation in Protein Aggregate Myopathies

(2009) Montse Olivé et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia

(2009) Conrad C. Weihl et al.   NEUROMUSCULAR DISORDERS

Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions

(2008) Yasushi Nishihira et al.   ACTA NEUROPATHOLOGICA

TDP-43 accumulation is common in myopathies with rimmed vacuoles

(2008) Benno Küsters et al.   ACTA NEUROPATHOLOGICA

Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia

(2008) Fumiaki Mori et al.   ACTA NEUROPATHOLOGICA

TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia

(2008) C C Weihl et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Inflammatory myopathies with mitochondrial pathology and protein aggregates

(2008) Peyker Temiz et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Axonal  -synuclein aggregates herald centripetal degeneration of cardiac sympathetic nerve in Parkinson's disease

(2007) S. Orimo et al.   BRAIN