4.6 Article

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

Related references

Note: Only part of the references are listed.
Article Clinical Neurology

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

Adam L. Boxer et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)

Article Multidisciplinary Sciences

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

Han-Xiang Deng et al.

NATURE (2011)

Editorial Material Clinical Neurology

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2010)

Article

Primary Central Nervous System Lymphoma

Elizabeth R. Gerstner et al.

ARCHIVES OF NEUROLOGY (2010)

Article Clinical Neurology

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Hannu Laaksovirta et al.

LANCET NEUROLOGY (2010)

Article Multidisciplinary Sciences

Mutations of optineurin in amyotrophic lateral sclerosis

Hirofumi Maruyama et al.

NATURE (2010)

Article Genetics & Heredity

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions

Vivianna M. Van Deerlin et al.

NATURE GENETICS (2010)

Article Neurosciences

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Jane O. Johnson et al.

NEURON (2010)

Article Multidisciplinary Sciences

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Jemeen Sreedharan et al.

SCIENCE (2008)

Review Clinical Neurology

The neuropathology and clinical phenotype of FTD with progranulin mutations

Ian R. A. Mackenzie

ACTA NEUROPATHOLOGICA (2007)

Article Pathology

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

Nigel J. Cairns et al.

AMERICAN JOURNAL OF PATHOLOGY (2007)

Article Clinical Neurology

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations

Manuela Neumann et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2007)

Article Biochemistry & Molecular Biology

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Tetsuaki Arai et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)

Article Multidisciplinary Sciences

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Manuela Neumann et al.

SCIENCE (2006)

Review Biotechnology & Applied Microbiology

Signaling, polyubiquitination, trafficking, and inclusions: Sequestosome 1/p62's role in neurodegenerative disease

Marie W. Wooten et al.

JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY (2006)