Dlouhy SR - Search Results

1

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.

Tagliavini F, Prelli F, Porro M, Rossi G, Giaccone G, Farlow MR, Dlouhy SR, Ghetti B, Bugiani O, Frangione B. Tagliavini F, et al. Among authors: dlouhy sr. Cell. 1994 Nov 18;79(4):695-703. doi: 10.1016/0092-8674(94)90554-1. Cell. 1994. PMID: 7954833

2

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. Among authors: dlouhy sr. Brain Pathol. 1995 Jan;5(1):61-75. doi: 10.1111/j.1750-3639.1995.tb00578.x. Brain Pathol. 1995. PMID: 7767492 Review.

3

Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.

Ghetti B, Tagliavini F, Giaccone G, Bugiani O, Frangione B, Farlow MR, Dlouhy SR. Ghetti B, et al. Among authors: dlouhy sr. Mol Neurobiol. 1994 Feb;8(1):41-8. doi: 10.1007/BF02778006. Mol Neurobiol. 1994. PMID: 7916191 Review.

4

Cerebrospinal fluid levels of amyloid beta-protein precursor are low in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.

Farlow M, Ghetti B, Dlouhy S, Giaccone G, Bugiani O, Tagliavini F, Wagner S. Farlow M, et al. Neurology. 1994 Aug;44(8):1508-10. doi: 10.1212/wnl.44.8.1508. Neurology. 1994. PMID: 8058158

5

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.

Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B. Dlouhy SR, et al. Nat Genet. 1992 Apr;1(1):64-7. doi: 10.1038/ng0492-64. Nat Genet. 1992. PMID: 1363809

6

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.

Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB. Hsiao K, et al. Among authors: dlouhy sr. Nat Genet. 1992 Apr;1(1):68-71. doi: 10.1038/ng0492-68. Nat Genet. 1992. PMID: 1363810

7

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family.

Ghetti B, Tagliavini F, Masters CL, Beyreuther K, Giaccone G, Verga L, Farlow MR, Conneally PM, Dlouhy SR, Azzarelli B, et al. Ghetti B, et al. Among authors: dlouhy sr. Neurology. 1989 Nov;39(11):1453-61. doi: 10.1212/wnl.39.11.1453. Neurology. 1989. PMID: 2573006

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. Among authors: dlouhy sr. J Neuropathol Exp Neurol. 1995 Nov;54(6):790-801. doi: 10.1097/00005072-199511000-00006. J Neuropathol Exp Neurol. 1995. PMID: 7595652

9

Prion protein amyloidosis.

Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F. Ghetti B, et al. Among authors: dlouhy sr. Brain Pathol. 1996 Apr;6(2):127-45. doi: 10.1111/j.1750-3639.1996.tb00796.x. Brain Pathol. 1996. PMID: 8737929 Review.

10

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. Among authors: dlouhy sr. J Neuropathol Exp Neurol. 1996 Nov;55(11):1157-63. doi: 10.1097/00005072-199611000-00007. J Neuropathol Exp Neurol. 1996. PMID: 8939199

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