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Links from PubMed

Items: 8

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
2.

[Analysis of mouse model exhibiting neurofibrillary changes].

Takashima A.

Rinsho Shinkeigaku. 2001 Dec;41(12):1111-2. Review. Japanese.

PMID:
12235811
3.

Neuropathology of familial tauopathy.

Tsuboi Y.

Neuropathology. 2006 Oct;26(5):471-4. Review.

PMID:
17080727
4.

Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course.

Saito Y, Kawai M, Inoue K, Sasaki R, Arai H, Nanba E, Kuzuhara S, Ihara Y, Kanazawa I, Murayama S.

J Neurol Sci. 2000 Aug 1;177(1):48-59. Review.

PMID:
10967182
5.
6.

[An autopsy case of "diffuse neurofibrillary tangles with calcification", multiple infarctions and hyaline arteriosclerosis].

Arai T, Kuroki N, Nizato K, Kase K, Iritani S, Ikeda K.

No To Shinkei. 1996 Jan;48(1):69-76. Review. Japanese.

PMID:
8679323
7.

[Diffuse neurofibrillary tangles with calcification].

Terada S, Kuroda S, Ishizu H, Tanabe Y.

Nihon Rinsho. 2004 Jan;62 Suppl:179-83. Review. Japanese. No abstract available.

PMID:
15011345
8.

[Tauopathy].

Kosaka S, Takuma H, Mori H.

Nihon Ronen Igakkai Zasshi. 2001 Sep;38(5):600-4. Review. Japanese. No abstract available.

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