NS-29822/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1994	1
1995	2
1996	1
1997	2
1998	2
2001	1
2003	1
2024	0

1

Sporadic and familial CJD: classification and characterisation.

Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Gambetti P, et al. Br Med Bull. 2003;66:213-39. doi: 10.1093/bmb/66.1.213. Br Med Bull. 2003. PMID: 14522861 Review.

2

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.

Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B. Piccardo P, et al. Am J Pathol. 2001 Jun;158(6):2201-7. doi: 10.1016/S0002-9440(10)64692-5. Am J Pathol. 2001. PMID: 11395398 Free PMC article.

3

Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.

Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, Nochlin D, Dickson DW, Vinters HV, Zimmerman TR, Mackenzie IR, Kish SJ, Ang LC, De Carli C, Pocchiari M, Brown P, Gibbs CJ Jr, Gajdusek DC, Bugiani O, Ironside J, Tagliavini F, Ghetti B. Piccardo P, et al. J Neuropathol Exp Neurol. 1998 Oct;57(10):979-88. doi: 10.1097/00005072-199810000-00010. J Neuropathol Exp Neurol. 1998. PMID: 9786248

4

An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy.

Piccardo P, Langeveld JP, Hill AF, Dlouhy SR, Young K, Giaccone G, Rossi G, Bugiani M, Bugiani O, Meloen RH, Collinge J, Tagliavini F, Ghetti B. Piccardo P, et al. Am J Pathol. 1998 Jun;152(6):1415-20. Am J Pathol. 1998. PMID: 9626045 Free PMC article.

5

Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S).

Unverzagt FW, Farlow MR, Norton J, Dlouhy SR, Young K, Ghetti B. Unverzagt FW, et al. J Int Neuropsychol Soc. 1997 Mar;3(2):169-78. J Int Neuropsychol Soc. 1997. PMID: 9126858

6

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. 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

7

Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).

Piccardo P, Seiler C, Dlouhy SR, Young K, Farlow MR, Prelli F, Frangione B, Bugiani O, Tagliavini F, Ghetti B. Piccardo P, et al. J Neuropathol Exp Neurol. 1996 Nov;55(11):1157-63. doi: 10.1097/00005072-199611000-00007. J Neuropathol Exp Neurol. 1996. PMID: 8939199

8

Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.

Piccardo P, Ghetti B, Dickson DW, Vinters HV, Giaccone G, Bugiani O, Tagliavini F, Young K, Dlouhy SR, Seiler C, et al. Piccardo P, et al. J Neuropathol Exp Neurol. 1995 Nov;54(6):790-801. doi: 10.1097/00005072-199511000-00006. J Neuropathol Exp Neurol. 1995. PMID: 7595652

9

Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.

Ghetti B, Dlouhy SR, Giaccone G, Bugiani O, Frangione B, Farlow MR, Tagliavini F. Ghetti B, et al. Brain Pathol. 1995 Jan;5(1):61-75. doi: 10.1111/j.1750-3639.1995.tb00578.x. Brain Pathol. 1995. PMID: 7767492 Review.

10

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B, et al. Monari L, et al. Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2839-42. doi: 10.1073/pnas.91.7.2839. Proc Natl Acad Sci U S A. 1994. PMID: 7908444 Free PMC article.

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