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Journal Abstract Search

798 related items for PubMed ID: 12734667

  • 21. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations.
    Josephs KA, Ahmed Z, Katsuse O, Parisi JF, Boeve BF, Knopman DS, Petersen RC, Davies P, Duara R, Graff-Radford NR, Uitti RJ, Rademakers R, Adamson J, Baker M, Hutton ML, Dickson DW.
    J Neuropathol Exp Neurol; 2007 Feb; 66(2):142-51. PubMed ID: 17278999
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  • 22. Upper motor neuron predominant degeneration with frontal and temporal lobe atrophy.
    Konagaya M, Sakai M, Matsuoka Y, Konagaya Y, Hashizume Y.
    Acta Neuropathol; 1998 Nov; 96(5):532-6. PubMed ID: 9829819
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  • 23. [A comparative immunohistochemical study of ubiquitin-positive skein-like inclusions in anterior horn neurons in subgroups of adult-onset motor neuron diseases].
    Matsumoto S, Kusaka H, Ito H, Yamasaki M, Imai T.
    Rinsho Shinkeigaku; 1993 Nov; 33(11):1125-30. PubMed ID: 8124868
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  • 24. An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions.
    Matsuoka T, Fujii N, Kondo A, Iwaki A, Hokonohara T, Honda H, Sasaki K, Suzuki SO, Iwaki T.
    Neuropathology; 2011 Feb; 31(1):71-6. PubMed ID: 20573033
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  • 28. Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease.
    Piao YS, Tan CF, Iwanaga K, Kakita A, Takano H, Nishizawa M, Lashley T, Revesz T, Lees A, de Silva R, Tsujihata M, Takahashi H.
    Acta Neuropathol; 2005 Dec; 110(6):600-9. PubMed ID: 16328530
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  • 29. Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.
    Lipton AM, White CL, Bigio EH.
    Acta Neuropathol; 2004 Nov; 108(5):379-85. PubMed ID: 15351890
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  • 30. Extrapyramidal features in patients with motor neuron disease and dementia; a clinicopathological correlative study.
    Mackenzie IR, Feldman H.
    Acta Neuropathol; 2004 Apr; 107(4):336-40. PubMed ID: 14745570
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  • 32. Neuronal inclusions in sporadic motor neuron disease are negative for alpha-synuclein.
    Sasaki S, Komori T, Iwata M.
    Neurosci Lett; 2004 Apr; 397(1-2):15-9. PubMed ID: 16406315
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  • 33. FUS pathology in basophilic inclusion body disease.
    Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, Kuroda S, Mackenzie IR.
    Acta Neuropathol; 2009 Nov; 118(5):617-27. PubMed ID: 19830439
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  • 34. Motor neurone disease-inclusion dementia.
    Jackson M, Lennox G, Lowe J.
    Neurodegeneration; 1996 Dec; 5(4):339-50. PubMed ID: 9117546
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  • 36. Familial frontotemporal dementia: a report of three cases of severe cerebral atrophy with rare inclusions that are negative for tau and synuclein, but positive for ubiquitin.
    Chang HT, Cortez S, Vonsattel JP, Stopa EG, Schelper RL.
    Acta Neuropathol; 2004 Jul; 108(1):10-6. PubMed ID: 15108011
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  • 37. Immunocytochemical and ultrastructural studies of lower motor neurons in amyotrophic lateral sclerosis.
    Murayama S, Mori H, Ihara Y, Bouldin TW, Suzuki K, Tomonaga M.
    Ann Neurol; 1990 Feb; 27(2):137-48. PubMed ID: 2156479
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  • 38. Neurofilament inclusion body disease with early onset frontotemporal dementia and primary lateral sclerosis.
    Mackenzie IR, Feldman H.
    Clin Neuropathol; 2004 Feb; 23(4):183-93. PubMed ID: 15328884
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  • 40. A case of frontotemporal lobar degeneration with ubiquitin-positive intraneuronal inclusions.
    Leel-Ossy L, Révész T, Almási K, Szucs I, Szabó E.
    Ideggyogy Sz; 2007 Jul 30; 60(7-8):330-5. PubMed ID: 17713114
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