Ghetti B - Search Results

1

White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration.

Kovacs GG, Majtenyi K, Spina S, Murrell JR, Gelpi E, Hoftberger R, Fraser G, Crowther RA, Goedert M, Budka H, Ghetti B. Kovacs GG, et al. Among authors: ghetti b. J Neuropathol Exp Neurol. 2008 Oct;67(10):963-75. doi: 10.1097/NEN.0b013e318187a80f. J Neuropathol Exp Neurol. 2008. PMID: 18800011 Free PMC article.

2

Spectrum of amyloid beta-protein immunoreactivity in hereditary Alzheimer disease with a guanine to thymine missense change at position 1924 of the APP gene.

Ghetti B, Murrell J, Benson MD, Farlow MR. Ghetti B, et al. Brain Res. 1992 Jan 31;571(1):133-9. doi: 10.1016/0006-8993(92)90519-f. Brain Res. 1992. PMID: 1611485

3

Clinical characteristics in a kindred with early-onset Alzheimer's disease and their linkage to a G-->T change at position 2149 of the amyloid precursor protein gene.

Farlow M, Murrell J, Ghetti B, Unverzagt F, Zeldenrust S, Benson M. Farlow M, et al. Among authors: ghetti b. Neurology. 1994 Jan;44(1):105-11. doi: 10.1212/wnl.44.1.105. Neurology. 1994. PMID: 8290042

4

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments.

Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MR, Ghetti B. Spillantini MG, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):4113-8. doi: 10.1073/pnas.94.8.4113. Proc Natl Acad Sci U S A. 1997. PMID: 9108114 Free PMC article.

5

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. Murrell JR, et al. Among authors: ghetti b. Am J Hum Genet. 1997 Nov;61(5):1131-8. doi: 10.1086/301594. Am J Hum Genet. 1997. PMID: 9345089 Free PMC article.

6

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.

Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B. Spillantini MG, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7737-41. doi: 10.1073/pnas.95.13.7737. Proc Natl Acad Sci U S A. 1998. PMID: 9636220 Free PMC article.

7

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. Mirra SS, et al. Among authors: ghetti b. J Neuropathol Exp Neurol. 1999 Apr;58(4):335-45. doi: 10.1097/00005072-199904000-00004. J Neuropathol Exp Neurol. 1999. PMID: 10218629

8

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, Morbin M, Primavera A, Carella F, Solaro C, Grisoli M, Savoiardo M, Spillantini MG, Tagliavini F, Goedert M, Ghetti B. Bugiani O, et al. Among authors: ghetti b. J Neuropathol Exp Neurol. 1999 Jun;58(6):667-77. doi: 10.1097/00005072-199906000-00011. J Neuropathol Exp Neurol. 1999. PMID: 10374757

9

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17.

Varani L, Hasegawa M, Spillantini MG, Smith MJ, Murrell JR, Ghetti B, Klug A, Goedert M, Varani G. Varani L, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):8229-34. doi: 10.1073/pnas.96.14.8229. Proc Natl Acad Sci U S A. 1999. PMID: 10393977 Free PMC article.

10

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. Delisle MB, et al. Among authors: ghetti b. Acta Neuropathol. 1999 Jul;98(1):62-77. doi: 10.1007/s004010051052. Acta Neuropathol. 1999. PMID: 10412802

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