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Results: 1 to 20 of 129

Similar articles for PubMed (Select 10202939)

1.

Tau gene mutation in familial progressive subcortical gliosis.

Goedert M, Spillantini MG, Crowther RA, Chen SG, Parchi P, Tabaton M, Lanska DJ, Markesbery WR, Wilhelmsen KC, Dickson DW, Petersen RB, Gambetti P.

Nat Med. 1999 Apr;5(4):454-7.

PMID:
10202939
2.

Case records of the Massachusetts General Hospital. Case 9-2015. A 31-year-old man with personality changes and progressive neurologic decline.

Miller BL, Dickerson BC, Lucente DE, Larvie M, Frosch MP.

N Engl J Med. 2015 Mar 19;372(12):1151-62. doi: 10.1056/NEJMcpc1409839. No abstract available.

PMID:
25785973
3.

Aprosodic speech with insular hyperintensities and 4R Tau pathology on autopsy.

Beldarrain MG, Ojeda JR, Ferrer I, Garcia-Monco JC.

Neurocase. 2013;19(6):583-6. doi: 10.1080/13554794.2012.713489. Epub 2012 Sep 20.

PMID:
22992154
4.

An overview of dementias.

Mathuranath PS.

Ann Indian Acad Neurol. 2010 Dec;13(Suppl 2):S54. doi: 10.4103/0972-2327.74245. No abstract available.

5.

DISCUSSION ON THE MENTAL AND PHYSICAL SYMPTOMS OF THE PRESENILE DEMENTIAS: Joint Discussion No. 5.

[No authors listed]

Proc R Soc Med. 1933 Jun;26(8):1077-91. No abstract available.

6.
7.

Subcortical neurofibrillary tangles and argyrophilic grains in a case of familial frontotemporal dementia with parkinsonism.

Kobayashi K, Sudo S, Matsubara R, Nakano H, Koshino Y.

Parkinsonism Relat Disord. 2008 Aug;14(6):513-6. doi: 10.1016/j.parkreldis.2007.10.015. Epub 2008 Mar 17.

PMID:
18346925
8.

The tau S305S mutation causes frontotemporal dementia with parkinsonism.

Skoglund L, Viitanen M, Kalimo H, Lannfelt L, J├Ânhagen ME, Ingelsson M, Glaser A, Herva R.

Eur J Neurol. 2008 Feb;15(2):156-61. Epub 2007 Dec 18.

PMID:
18093153
9.

Familial early-onset dementia with tau intron 10 + 16 mutation with clinical features similar to those of Alzheimer disease.

Doran M, du Plessis DG, Ghadiali EJ, Mann DM, Pickering-Brown S, Larner AJ.

Arch Neurol. 2007 Oct;64(10):1535-9.

PMID:
17923640
10.
11.

Frontotemporal dementia with tau pathology.

Gasparini L, Terni B, Spillantini MG.

Neurodegener Dis. 2007;4(2-3):236-53. Review.

PMID:
17596718
12.
13.

Cortical neuronal and glial pathology in TgTauP301L transgenic mice: neuronal degeneration, memory disturbance, and phenotypic variation.

Murakami T, Paitel E, Kawarabayashi T, Ikeda M, Chishti MA, Janus C, Matsubara E, Sasaki A, Kawarai T, Phinney AL, Harigaya Y, Horne P, Egashira N, Mishima K, Hanna A, Yang J, Iwasaki K, Takahashi M, Fujiwara M, Ishiguro K, Bergeron C, Carlson GA, Abe K, Westaway D, St George-Hyslop P, Shoji M.

Am J Pathol. 2006 Oct;169(4):1365-75.

14.

Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes.

Sakai K, Piao YS, Kikugawa K, Ohara S, Hasegawa M, Takano H, Fukase M, Nishizawa M, Kakita A, Takahashi H.

Acta Neuropathol. 2006 Sep;112(3):341-8. Epub 2006 Jun 28.

PMID:
16804710
15.

Frontal temporal dementia: dissecting the aetiology and pathogenesis.

Hardy J, Momeni P, Traynor BJ.

Brain. 2006 Apr;129(Pt 4):830-1. No abstract available.

16.

A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia.

Malkani R, D'Souza I, Gwinn-Hardy K, Schellenberg GD, Hardy J, Momeni P.

Neurobiol Dis. 2006 May;22(2):401-3. Epub 2006 Feb 28.

PMID:
16503405
17.

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. Epub 2005 Nov 22.

PMID:
16328530
18.

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation.

Shi J, Shaw CL, Du Plessis D, Richardson AM, Bailey KL, Julien C, Stopford C, Thompson J, Varma A, Craufurd D, Tian J, Pickering-Brown S, Neary D, Snowden JS, Mann DM.

Acta Neuropathol. 2005 Nov;110(5):501-12. Epub 2005 Oct 13.

PMID:
16222525
19.

Tau gene mutations and their effects.

Goedert M.

Mov Disord. 2005 Aug;20 Suppl 12:S45-52.

PMID:
16092090
20.

Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.

Bronner IF, ter Meulen BC, Azmani A, Severijnen LA, Willemsen R, Kamphorst W, Ravid R, Heutink P, van Swieten JC.

Brain. 2005 Nov;128(Pt 11):2645-53. Epub 2005 Jul 13.

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