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Journal Abstract Search

301 related items for PubMed ID: 16106222

  • 1. Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum.
    Mackenzie IR, Feldman HH.
    J Neuropathol Exp Neurol; 2005 Aug; 64(8):730-9. PubMed ID: 16106222
    [Abstract] [Full Text] [Related]

  • 2. Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases.
    Mackenzie IR, Feldman H.
    Acta Neuropathol; 2003 Jun; 105(6):543-8. PubMed ID: 12734660
    [Abstract] [Full Text] [Related]

  • 3. Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases.
    Mackenzie IR, Feldman H.
    Dement Geriatr Cogn Disord; 2004 Jun; 17(4):333-6. PubMed ID: 15178948
    [Abstract] [Full Text] [Related]

  • 4. The relationship between extramotor ubiquitin-immunoreactive neuronal inclusions and dementia in motor neuron disease.
    Mackenzie IR, Feldman H.
    Acta Neuropathol; 2003 Feb; 105(2):98-102. PubMed ID: 12536219
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.
    Bigio EH, Johnson NA, Rademaker AW, Fung BB, Mesulam MM, Siddique N, Dellefave L, Caliendo J, Freeman S, Siddique T.
    J Neuropathol Exp Neurol; 2004 Aug; 63(8):801-11. PubMed ID: 15330335
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Ubiquitin immunohistochemistry of frontotemporal lobar degeneration differentiates cases with and without motor neuron disease.
    Katsuse O, Dickson DW.
    Alzheimer Dis Assoc Disord; 2005 Nov; 19 Suppl 1():S37-43. PubMed ID: 16317257
    [Abstract] [Full Text] [Related]

  • 9. TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.
    Seelaar H, Schelhaas HJ, Azmani A, Küsters B, Rosso S, Majoor-Krakauer D, de Rijk MC, Rizzu P, ten Brummelhuis M, van Doorn PA, Kamphorst W, Willemsen R, van Swieten JC.
    Brain; 2007 May; 130(Pt 5):1375-85. PubMed ID: 17360763
    [Abstract] [Full Text] [Related]

  • 10. Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease.
    Brandmeir NJ, Geser F, Kwong LK, Zimmerman E, Qian J, Lee VM, Trojanowski JQ.
    Acta Neuropathol; 2008 Jan; 115(1):123-31. PubMed ID: 18004574
    [Abstract] [Full Text] [Related]

  • 11. Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study.
    Kövari E, Gold G, Giannakopoulos P, Bouras C.
    Acta Neuropathol; 2004 Sep; 108(3):207-12. PubMed ID: 15170577
    [Abstract] [Full Text] [Related]

  • 12. Ubiquitin-positive neuronal and tau 2-positive glial inclusions in frontotemporal dementia of motor neuron type.
    Forno LS, Langston JW, Herrick MK, Wilson JD, Murayama S.
    Acta Neuropathol; 2002 Jun; 103(6):599-606. PubMed ID: 12012092
    [Abstract] [Full Text] [Related]

  • 13. Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions? Report of an autopsy case and a review of the literature.
    Tan CF, Kakita A, Piao YS, Kikugawa K, Endo K, Tanaka M, Okamoto K, Takahashi H.
    Acta Neuropathol; 2003 Jun; 105(6):615-20. PubMed ID: 12734667
    [Abstract] [Full Text] [Related]

  • 14. Ubiquitin-only intraneuronal inclusion in the substantia nigra is a characteristic feature of motor neurone disease with dementia.
    Al-Sarraj S, Maekawa S, Kibble M, Everall I, Leigh N.
    Neuropathol Appl Neurobiol; 2002 Apr; 28(2):120-8. PubMed ID: 11972798
    [Abstract] [Full Text] [Related]

  • 15. [Clinico-pathological investigation of two patients with dementia with motor neuron disease].
    Yamamoto R, Iseki E, Murayama N, Minegishi M, Kimura M, Eto K, Arai H, Ohbu S, Hatanaka D, Hino H, Fujisawa K.
    Brain Nerve; 2007 Mar; 59(3):263-9. PubMed ID: 17370652
    [Abstract] [Full Text] [Related]

  • 16. White matter lesions in the brain with frontotemporal lobar degeneration with motor neuron disease: TDP-43-immunopositive inclusions co-localize with p62, but not ubiquitin.
    Hiji M, Takahashi T, Fukuba H, Yamashita H, Kohriyama T, Matsumoto M.
    Acta Neuropathol; 2008 Aug; 116(2):183-91. PubMed ID: 18584184
    [Abstract] [Full Text] [Related]

  • 17. Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease.
    Josephs KA, Parisi JE, Knopman DS, Boeve BF, Petersen RC, Dickson DW.
    Arch Neurol; 2006 Apr; 63(4):506-12. PubMed ID: 16606762
    [Abstract] [Full Text] [Related]

  • 18. Clinical entity of frontotemporal dementia with motor neuron disease.
    Mitsuyama Y, Inoue T.
    Neuropathology; 2009 Dec; 29(6):649-54. PubMed ID: 19780984
    [Abstract] [Full Text] [Related]

  • 19. Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.
    Davidson Y, Kelley T, Mackenzie IR, Pickering-Brown S, Du Plessis D, Neary D, Snowden JS, Mann DM.
    Acta Neuropathol; 2007 May; 113(5):521-33. PubMed ID: 17219193
    [Abstract] [Full Text] [Related]

  • 20. Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia.
    Holton JL, Révész T, Crooks R, Scaravilli F.
    Acta Neuropathol; 2002 Mar; 103(3):221-7. PubMed ID: 11907801
    [Abstract] [Full Text] [Related]

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