Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 90

Similar articles for PubMed (Select 7783864)

1.

Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17.

Petersen RB, Tabaton M, Chen SG, Monari L, Richardson SL, Lynch T, Manetto V, Lanska DJ, Markesbery WR, Lynches T [corrected to Lynch T], et al.

Neurology. 1995 Jun;45(6):1062-7. Erratum in: Neurology 1995 Jul;45(7):1430.

PMID:
7783864
2.

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.

Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P, et al.

N Engl J Med. 1992 Feb 13;326(7):444-9.

3.

Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene.

Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F.

Neurology. 2000 Aug 8;55(3):405-10.

PMID:
10932276
4.

Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques.

Ishida C, Kakishima A, Okino S, Furukawa Y, Kano M, Oda Y, Nakanishi I, Makifuchi T, Kitamoto T, Yamada M.

Neurology. 2003 Feb 11;60(3):514-7.

PMID:
12578942
5.

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

Chiesa R, Piccardo P, Ghetti B, Harris DA.

Neuron. 1998 Dec;21(6):1339-51.

6.

Tau gene mutation in familial progressive subcortical gliosis.

Goedert M, Spillantini MG, Crowther RA, Chen SG, Parchi P, Tabaton M, Lanska DJ, Markesbery WR, Wilhelmsen KC, Dickson DW, Petersen RB, Gambetti P.

Nat Med. 1999 Apr;5(4):454-7.

PMID:
10202939
7.

Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease.

Ishida C, Okino S, Kitamoto T, Yamada M.

J Neurol Neurosurg Psychiatry. 2005 Mar;76(3):325-9.

8.

Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms.

Bossers A, Belt PBGM, Raymond GJ, Caughey B, de Vries R, Smits MA.

Proc Natl Acad Sci U S A. 1997 May 13;94(10):4931-6.

9.

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P.

Ann Neurol. 1996 Jun;39(6):767-78.

PMID:
8651649
10.

Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes.

Zanusso G, Farinazzo A, Prelli F, Fiorini M, Gelati M, Ferrari S, Righetti PG, Rizzuto N, Frangione B, Monaco S.

J Biol Chem. 2004 Sep 10;279(37):38936-42. Epub 2004 Jul 9.

11.

Loss of glycosylation associated with the T183A mutation in human prion disease.

Grasbon-Frodl E, Lorenz H, Mann U, Nitsch RM, Windl O, Kretzschmar HA.

Acta Neuropathol. 2004 Dec;108(6):476-84. Epub 2004 Oct 26.

PMID:
15558291
12.

Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.

Gelpi E, Kovacs GG, Ströbel T, Koperek O, Voigtländer T, Liberski PP, Budka H.

Acta Neuropathol. 2005 Nov;110(5):513-9. Epub 2005 Sep 10.

PMID:
16155763
13.

Prion encephalopathies of animals and humans.

Prusiner SB.

Dev Biol Stand. 1993;80:31-44. Review.

PMID:
8270114
14.
15.

Allelic origin of the abnormal prion protein isoform in familial prion diseases.

Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P.

Nat Med. 1997 Sep;3(9):1009-15.

PMID:
9288728
16.

The spectrum of transmissible spongiform encephalopathies.

Weber T, Aguzzi A.

Intervirology. 1997;40(2-3):198-212. Review.

PMID:
9450236
17.

A case of progressive subcortical gliosis associated with deposition of abnormal prion protein (PrP)

Revesz T, Daniel SE, Lees AJ, Will RG.

J Neurol Neurosurg Psychiatry. 1995 Jun;58(6):759-60. No abstract available.

18.

[Biology of non-conventional transmissible agents or prions].

Dormont D.

Rev Neurol (Paris). 1998 Feb;154(2):142-51. Review. French.

PMID:
9773035
19.

Huntington disease phenocopy is a familial prion disease.

Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edström L, Anvret M, Prusiner SB.

Am J Hum Genet. 2001 Dec;69(6):1385-8. Epub 2001 Oct 9.

20.

Cerebral amyloid in human prion disease.

Watanabe R, Duchen LW.

Neuropathol Appl Neurobiol. 1993 Jun;19(3):253-60.

PMID:
8355811
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk