Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 112

1.

A distinct familial presenile dementia with a novel missense mutation in the tau gene.

Iijima M, Tabira T, Poorkaj P, Schellenberg GD, Trojanowski JQ, Lee VM, Schmidt ML, Takahashi K, Nabika T, Matsumoto T, Yamashita Y, Yoshioka S, Ishino H.

Neuroreport. 1999 Feb 25;10(3):497-501.

PMID:
10208578
[PubMed - indexed for MEDLINE]
2.

Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.

Iseki E, Matsumura T, Marui W, Hino H, Odawara T, Sugiyama N, Suzuki K, Sawada H, Arai T, Kosaka K.

Acta Neuropathol. 2001 Sep;102(3):285-92.

PMID:
11585254
[PubMed - indexed for MEDLINE]
3.

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.

Delisle MB, Murrell JR, Richardson R, Trofatter JA, Rascol O, Soulages X, Mohr M, Calvas P, Ghetti B.

Acta Neuropathol. 1999 Jul;98(1):62-77.

PMID:
10412802
[PubMed - indexed for MEDLINE]
4.

Tau pathology in a family with dementia and a P301L mutation in tau.

Mirra SS, Murrell JR, Gearing M, Spillantini MG, Goedert M, Crowther RA, Levey AI, Jones R, Green J, Shoffner JM, Wainer BH, Schmidt ML, Trojanowski JQ, Ghetti B.

J Neuropathol Exp Neurol. 1999 Apr;58(4):335-45.

PMID:
10218629
[PubMed - indexed for MEDLINE]
5.

Familial parkinsonism and dementia with ballooned neurons, argyrophilic neuronal inclusions, atypical neurofibrillary tangles, tau-negative astrocytic fibrillary tangles, and Lewy bodies.

Mizutani T, Inose T, Nakajima S, Kakimi S, Uchigata M, Ikeda K, Gambetti P, Takasu T.

Acta Neuropathol. 1998 Jan;95(1):15-27.

PMID:
9452818
[PubMed - indexed for MEDLINE]
6.

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.

Pickering-Brown SM, Richardson AM, Snowden JS, McDonagh AM, Burns A, Braude W, Baker M, Liu WK, Yen SH, Hardy J, Hutton M, Davies Y, Allsop D, Craufurd D, Neary D, Mann DM.

Brain. 2002 Apr;125(Pt 4):732-51.

PMID:
11912108
[PubMed - indexed for MEDLINE]
Free Article
7.

A new case of frontotemporal dementia and parkinsonism resulting from an intron 10 +3-splice site mutation in the tau gene: clinical and pathological features.

Tolnay M, Grazia Spillantini M, Rizzini C, Eccles D, Lowe J, Ellison D.

Neuropathol Appl Neurobiol. 2000 Aug;26(4):368-78.

PMID:
10931371
[PubMed - indexed for MEDLINE]
8.

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.

Lossos A, Reches A, Gal A, Newman JP, Soffer D, Gomori JM, Boher M, Ekstein D, Biran I, Meiner Z, Abramsky O, Rosenmann H.

J Neurol. 2003 Jun;250(6):733-40.

PMID:
12796837
[PubMed - indexed for MEDLINE]
9.

An autopsy case of diffuse neurofibrillary tangles with calcification: early stage pathologic findings.

Iwasaki Y, Ito M, Mori K, Deguchi A, Nagaoka M, Yoshida M, Hashizume Y.

Neuropathology. 2009 Dec;29(6):697-703. doi: 10.1111/j.1440-1789.2009.01003.x. Epub 2009 Mar 3.

PMID:
19389080
[PubMed - indexed for MEDLINE]
10.

Autosomal dominant dementia with widespread neurofibrillary tangles.

Reed LA, Grabowski TJ, Schmidt ML, Morris JC, Goate A, Solodkin A, Van Hoesen GW, Schelper RL, Talbot CJ, Wragg MA, Trojanowski JQ.

Ann Neurol. 1997 Oct;42(4):564-72.

PMID:
9382467
[PubMed - indexed for MEDLINE]
11.

Selective expression of Ser 199/202 phosphorylated tau in a case of frontotemporal dementia.

Takamatsu J, Kondo A, Ikegami K, Kimura T, Fujii H, Mitsuyama Y, Hashizume Y.

Dement Geriatr Cogn Disord. 1998 Mar-Apr;9(2):82-9.

PMID:
9524799
[PubMed - indexed for MEDLINE]
12.

Tau-positive fine granules in the cerebral white matter: a novel finding among the tauopathies exclusive to parkinsonism-dementia complex of Guam.

Yamazaki M, Hasegawa M, Mori O, Murayama S, Tsuchiya K, Ikeda K, Chen KM, Katayama Y, Oyanagi K.

J Neuropathol Exp Neurol. 2005 Oct;64(10):839-46.

PMID:
16215455
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

[An autopsied case of atypical presenile dementia which shows lobar atrophy, severe neurofibrillary tangles and calcification].

Ujihira N, Hashizume Y, Takagi T, Ito M.

Rinsho Shinkeigaku. 1997 Apr;37(4):292-9. Japanese.

PMID:
9248337
[PubMed - indexed for MEDLINE]
15.

A clinical and pathological study of a Japanese case of Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex with family history.

Konagaya M, Kato T, Sakai M, Kuru S, Matsuoka Y, Konagaya Y, Hashizume Y, Tabira T.

J Neurol. 2003 Feb;250(2):164-70.

PMID:
12574946
[PubMed - indexed for MEDLINE]
16.

The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein.

Taniguchi S, McDonagh AM, Pickering-Brown SM, Umeda Y, Iwatsubo T, Hasegawa M, Mann DM.

Neuropathol Appl Neurobiol. 2004 Feb;30(1):1-18.

PMID:
14720172
[PubMed - indexed for MEDLINE]
17.

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

Bird TD, Nochlin D, Poorkaj P, Cherrier M, Kaye J, Payami H, Peskind E, Lampe TH, Nemens E, Boyer PJ, Schellenberg GD.

Brain. 1999 Apr;122 ( Pt 4):741-56. Erratum in: Brain 1999 Jul;122(Pt 7):1398.

PMID:
10219785
[PubMed - indexed for MEDLINE]
Free Article
18.

Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation.

Ferrer I, Pastor P, Rey MJ, Muñoz E, Puig B, Pastor E, Oliva R, Tolosa E.

Neuropathol Appl Neurobiol. 2003 Feb;29(1):23-34.

PMID:
12581337
[PubMed - indexed for MEDLINE]
19.

Tau pathology in diffuse neurofibrillary tangles with calcification (DNTC): biochemical and immunohistochemical investigation.

Tanabe Y, Ishizu H, Ishiguro K, Itoh N, Terada S, Haraguchi T, Kawai K, Kuroda S.

Neuroreport. 2000 Aug 3;11(11):2473-7.

PMID:
10943706
[PubMed - indexed for MEDLINE]
20.

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.

Arima K, Kowalska A, Hasegawa M, Mukoyama M, Watanabe R, Kawai M, Takahashi K, Iwatsubo T, Tabira T, Sunohara N.

Neurology. 2000 May 9;54(9):1787-95.

PMID:
10802785
[PubMed - indexed for MEDLINE]
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk