Piccardo P - Search Results

1

Association between conformational mutations in neuroserpin and onset and severity of dementia.

Davis RL, Shrimpton AE, Carrell RW, Lomas DA, Gerhard L, Baumann B, Lawrence DA, Yepes M, Kim TS, Ghetti B, Piccardo P, Takao M, Lacbawan F, Muenke M, Sifers RN, Bradshaw CB, Kent PF, Collins GH, Larocca D, Holohan PD. Davis RL, et al. Among authors: piccardo p. Lancet. 2002 Jun 29;359(9325):2242-7. doi: 10.1016/S0140-6736(02)09293-0. Lancet. 2002. PMID: 12103288

2

Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.

Takao M, Benson MD, Murrell JR, Yazaki M, Piccardo P, Unverzagt FW, Davis RL, Holohan PD, Lawrence DA, Richardson R, Farlow MR, Ghetti B. Takao M, et al. Among authors: piccardo p. J Neuropathol Exp Neurol. 2000 Dec;59(12):1070-86. doi: 10.1093/jnen/59.12.1070. J Neuropathol Exp Neurol. 2000. PMID: 11138927

3

Biochemical characterization of a neuroserpin variant associated with hereditary dementia.

Yazaki M, Liepnieks JJ, Murrell JR, Takao M, Guenther B, Piccardo P, Farlow MR, Ghetti B, Benson MD. Yazaki M, et al. Among authors: piccardo p. Am J Pathol. 2001 Jan;158(1):227-33. doi: 10.1016/S0002-9440(10)63961-2. Am J Pathol. 2001. PMID: 11141496 Free PMC article.

4

Early-onset dementia with Lewy bodies.

Takao M, Ghetti B, Yoshida H, Piccardo P, Narain Y, Murrell JR, Vidal R, Glazier BS, Jakes R, Tsutsui M, Spillantini MG, Crowther RA, Goedert M, Koto A. Takao M, et al. Among authors: piccardo p. Brain Pathol. 2004 Apr;14(2):137-47. doi: 10.1111/j.1750-3639.2004.tb00046.x. Brain Pathol. 2004. PMID: 15193026 Free PMC article.

5

Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker.

Ghetti B, Piccardo P, Zanusso G. Ghetti B, et al. Among authors: piccardo p. Handb Clin Neurol. 2018;153:243-269. doi: 10.1016/B978-0-444-63945-5.00014-3. Handb Clin Neurol. 2018. PMID: 29887140

6

Hereditary prion protein amyloidoses.

Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P. Ghetti B, et al. Among authors: piccardo p. Clin Lab Med. 2003 Mar;23(1):65-85, viii. doi: 10.1016/s0272-2712(02)00064-1. Clin Lab Med. 2003. PMID: 12733425 Review.

7

Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129.

Young K, Clark HB, Piccardo P, Dlouhy SR, Ghetti B. Young K, et al. Among authors: piccardo p. Brain Res Mol Brain Res. 1997 Feb;44(1):147-50. doi: 10.1016/s0169-328x(96)00251-3. Brain Res Mol Brain Res. 1997. PMID: 9030710

8

Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein.

Stewart RS, Piccardo P, Ghetti B, Harris DA. Stewart RS, et al. Among authors: piccardo p. J Neurosci. 2005 Mar 30;25(13):3469-77. doi: 10.1523/JNEUROSCI.0105-05.2005. J Neurosci. 2005. PMID: 15800202 Free PMC article.

9

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

Chiesa R, Piccardo P, Ghetti B, Harris DA. Chiesa R, et al. Among authors: piccardo p. Neuron. 1998 Dec;21(6):1339-51. doi: 10.1016/s0896-6273(00)80653-4. Neuron. 1998. PMID: 9883727 Free article.

10

Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.

Chiesa R, Piccardo P, Biasini E, Ghetti B, Harris DA. Chiesa R, et al. Among authors: piccardo p. J Neurosci. 2008 Dec 3;28(49):13258-67. doi: 10.1523/JNEUROSCI.3109-08.2008. J Neurosci. 2008. PMID: 19052217 Free PMC article.

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