Works matching IS 09196544 AND DT 2014 AND VI 34 AND IP 1
Results: 16
Niemann- Pick disease type C1 predominantly involving the frontotemporal region, with cortical and brainstem Lewy bodies: An autopsy case.
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- Neuropathology, 2014, v. 34, n. 1, p. 49, doi. 10.1111/neup.12047
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Adenoviral expression of TDP-43 and FUS genes and shRNAs for protein degradation pathways in rodent motoneurons in vitro and in vivo.
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- Neuropathology, 2014, v. 34, n. 1, p. 83, doi. 10.1111/neup.12058
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Cover Image.
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- Neuropathology, 2014, v. 34, n. 1, p. i, doi. 10.1111/neup.12098
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Novel neuronal cytoplasmic inclusions in a patient carrying SCA8 expansion mutation.
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- Neuropathology, 2014, v. 34, n. 1, p. 27, doi. 10.1111/neup.12042
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TDP-43 pathology in polyglutamine diseases: With reference to amyotrphic lateral sclerosis.
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- Neuropathology, 2014, v. 34, n. 1, p. 77, doi. 10.1111/neup.12053
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Cryptococcal meningitis accompanying lymphocytic inflammation predominantly in cerebral deep white matter: A possible manifestation of immune reconstitution inflammatory syndrome.
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- Neuropathology, 2014, v. 34, n. 1, p. 45, doi. 10.1111/neup.12046
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Minor splicing pathway is not minor any more: Implications for the pathogenesis of motor neuron diseases.
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- Neuropathology, 2014, v. 34, n. 1, p. 99, doi. 10.1111/neup.12070
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Neuronal differentiation associated with Gli3 expression predicts favorable outcome for patients with medulloblastoma.
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- Neuropathology, 2014, v. 34, n. 1, p. 1, doi. 10.1111/neup.12052
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Issue Information.
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- Neuropathology, 2014, v. 34, n. 1, p. ii, doi. 10.1111/neup.12063
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Inflammatory infratentorial progressive multifocal leukoencephalopathy in a patient with rheumatoid arthritis.
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- Neuropathology, 2014, v. 34, n. 1, p. 39, doi. 10.1111/neup.12045
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ALS-associated protein FIG4 is localized in Pick and Lewy bodies, and also neuronal nuclear inclusions, in polyglutamine and intranuclear inclusion body diseases.
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- Neuropathology, 2014, v. 34, n. 1, p. 19, doi. 10.1111/neup.12056
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An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation.
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- Neuropathology, 2014, v. 34, n. 1, p. 58, doi. 10.1111/neup.12049
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Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation.
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- Neuropathology, 2014, v. 34, n. 1, p. 64, doi. 10.1111/neup.12051
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Co-localization of Bunina bodies and TDP-43 inclusions in lower motor neurons in amyotrophic lateral sclerosis.
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- Neuropathology, 2014, v. 34, n. 1, p. 71, doi. 10.1111/neup.12044
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Immunohistochemical analysis of ubiquilin-1 in the human hippocampus: Association with neurofibrillary tangle pathology.
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- Neuropathology, 2014, v. 34, n. 1, p. 11, doi. 10.1111/neup.12055
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Anaplastic oligodendroglioma arising from the brain stem and featuring 1p/19q co-deletion.
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- Neuropathology, 2014, v. 34, n. 1, p. 32, doi. 10.1111/neup.12043
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