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Results: 8

1.

Pathologic evidence that the T188R mutation in PRNP is associated with prion disease.

Tartaglia MC, Thai JN, See T, Kuo A, Harbaugh R, Raudabaugh B, Cali I, Sattavat M, Sanchez H, DeArmond SJ, Geschwind MD.

J Neuropathol Exp Neurol. 2010 Dec;69(12):1220-7. doi: 10.1097/NEN.0b013e3181ffc39c.

PMID:
21107135
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype.

Ghoshal N, Cali I, Perrin RJ, Josephson SA, Sun N, Gambetti P, Morris JC.

Arch Neurol. 2009 Oct;66(10):1240-6. doi: 10.1001/archneurol.2009.224.

PMID:
19822779
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family.

Spina S, Farlow MR, Unverzagt FW, Kareken DA, Murrell JR, Fraser G, Epperson F, Crowther RA, Spillantini MG, Goedert M, Ghetti B.

Brain. 2008 Jan;131(Pt 1):72-89. Epub 2007 Dec 7.

PMID:
18065436
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P.

Am J Hum Genet. 1999 Feb;64(2):414-21.

PMID:
9973279
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau.

Spillantini MG, Crowther RA, Kamphorst W, Heutink P, van Swieten JC.

Am J Pathol. 1998 Nov;153(5):1359-63.

PMID:
9811325
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B.

Am J Hum Genet. 1997 Nov;61(5):1131-8.

PMID:
9345089
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genes and parkinsonism.

Wood N.

J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):305-9. No abstract available.

PMID:
9120440
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)

Vidal R, Garzuly F, Budka H, Lalowski M, Linke RP, Brittig F, Frangione B, Wisniewski T.

Am J Pathol. 1996 Feb;148(2):361-6.

PMID:
8579098
[PubMed - indexed for MEDLINE]
Free PMC Article

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