Ghetti B - Search Results

1

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, Budka H, Ghetti B, Spina S. Kovacs GG, et al. Among authors: ghetti b. Mov Disord. 2009 Sep 15;24(12):1843-7. doi: 10.1002/mds.22697. Mov Disord. 2009. PMID: 19609911

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

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease.

Murrell J, Farlow M, Ghetti B, Benson MD. Murrell J, et al. Among authors: ghetti b. Science. 1991 Oct 4;254(5028):97-9. doi: 10.1126/science.1925564. Science. 1991. PMID: 1925564

4

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

5

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.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

562 results

Search Page