Works matching IS 00016322 AND DT 2011 AND VI 122 AND IP 6
Results: 14
Fas/FasL-mediated apoptosis and inflammation are key features of acute human spinal cord injury: implications for translational, clinical application.
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- Acta Neuropathologica, 2011, v. 122, n. 6, p. 747, doi. 10.1007/s00401-011-0882-3
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- Publication type:
- Article
Simulated brain biopsy for diagnosing neurodegeneration using autopsy-confirmed cases.
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- Acta Neuropathologica, 2011, v. 122, n. 6, p. 737, doi. 10.1007/s00401-011-0880-5
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- Publication type:
- Article
A proteomic study identifies different levels of light chain ferritin in corticobasal degeneration and progressive supranuclear palsy.
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- Acta Neuropathologica, 2011, v. 122, n. 6, p. 727, doi. 10.1007/s00401-011-0888-x
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- Publication type:
- Article
Activating L265P mutations of the MYD88 gene are common in primary central nervous system lymphoma.
- Published in:
- 2011
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- Publication type:
- Letter
Multinodular leptomeningeal metastases from ETANTR contain both small blue cell and maturing neuropil elements.
- Published in:
- 2011
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- Publication type:
- Letter
Inner ear lesions in congenital cytomegalovirus infection of human fetuses.
- Published in:
- Acta Neuropathologica, 2011, v. 122, n. 6, p. 763, doi. 10.1007/s00401-011-0895-y
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- Publication type:
- Article
TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's Syndrome: association with age, hippocampal sclerosis and clinical phenotype.
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- Acta Neuropathologica, 2011, v. 122, n. 6, p. 703, doi. 10.1007/s00401-011-0879-y
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- Publication type:
- Article
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with loss of morphological but retained genetic key features during progression.
- Published in:
- 2011
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- Publication type:
- Letter
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72.
- Published in:
- Acta Neuropathologica, 2011, v. 122, n. 6, p. 673, doi. 10.1007/s00401-011-0907-y
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- Publication type:
- 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.
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- Acta Neuropathologica, 2011, v. 122, n. 6, p. 691, doi. 10.1007/s00401-011-0911-2
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- Publication type:
- Article
Acute and chronically increased immunoreactivity to phosphorylation-independent but not pathological TDP-43 after a single traumatic brain injury in humans.
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- Acta Neuropathologica, 2011, v. 122, n. 6, p. 715, doi. 10.1007/s00401-011-0909-9
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- Publication type:
- Article
C9ORF72, the new gene on the block, causes C9FTD/ALS: new insights provided by neuropathology.
- Published in:
- 2011
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- Publication type:
- Editorial
An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene.
- Published in:
- 2011
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- Publication type:
- Report
Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology.
- Published in:
- Acta Neuropathologica, 2011, v. 122, n. 6, p. 657, doi. 10.1007/s00401-011-0913-0
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- Publication type:
- Article