Ghetti B - Search Results

1

Structures of α-synuclein filaments from multiple system atrophy.

Schweighauser M, Shi Y, Tarutani A, Kametani F, Murzin AG, Ghetti B, Matsubara T, Tomita T, Ando T, Hasegawa K, Murayama S, Yoshida M, Hasegawa M, Scheres SHW, Goedert M. Schweighauser M, et al. Among authors: ghetti b. Nature. 2020 Sep;585(7825):464-469. doi: 10.1038/s41586-020-2317-6. Epub 2020 May 27. Nature. 2020. PMID: 32461689 Free PMC article.

2

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.

3

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.

4

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.

5

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

Murrell JR, Spillantini MG, Zolo P, Guazzelli M, Smith MJ, Hasegawa M, Redi F, Crowther RA, Pietrini P, Ghetti B, Goedert M. Murrell JR, et al. Among authors: ghetti b. J Neuropathol Exp Neurol. 1999 Dec;58(12):1207-26. doi: 10.1097/00005072-199912000-00002. J Neuropathol Exp Neurol. 1999. PMID: 10604746

6

Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.

Ghetti B, Murrell JR, Zolo P, Spillantini MG, Goedert M. Ghetti B, et al. Ann N Y Acad Sci. 2000;920:52-62. doi: 10.1111/j.1749-6632.2000.tb06905.x. Ann N Y Acad Sci. 2000. PMID: 11193177

7

Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Their relevance for understanding the neurogenerative process.

Goedert M, Ghetti B, Spillantini MG. Goedert M, et al. Among authors: ghetti b. Ann N Y Acad Sci. 2000;920:74-83. doi: 10.1111/j.1749-6632.2000.tb06907.x. Ann N Y Acad Sci. 2000. PMID: 11193179 Review.

8

The novel Tau mutation G335S: clinical, neuropathological and molecular characterization.

Spina S, Murrell JR, Yoshida H, Ghetti B, Bermingham N, Sweeney B, Dlouhy SR, Crowther RA, Goedert M, Keohane C. Spina S, et al. Among authors: ghetti b. Acta Neuropathol. 2007 Apr;113(4):461-70. doi: 10.1007/s00401-006-0182-5. Epub 2006 Dec 22. Acta Neuropathol. 2007. PMID: 17186252

9

Alois Alzheimer: his life and times.

Goedert M, Ghetti B. Goedert M, et al. Among authors: ghetti b. Brain Pathol. 2007 Jan;17(1):57-62. doi: 10.1111/j.1750-3639.2007.00056.x. Brain Pathol. 2007. PMID: 17493039 Free PMC article.

10

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. Spina S, et al. Among authors: ghetti b. Brain. 2008 Jan;131(Pt 1):72-89. doi: 10.1093/brain/awm280. Epub 2007 Dec 7. Brain. 2008. PMID: 18065436 Free PMC article.

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