Gambetti P - Search Results

1

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy.

Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG. Dagvadorj A, et al. Among authors: gambetti p. Ann Neurol. 2002 Sep;52(3):355-9. doi: 10.1002/ana.10267. Ann Neurol. 2002. PMID: 12205650

2

Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study.

Bütefisch CM, Gambetti P, Cervenakova L, Park KY, Hallett M, Goldfarb LG. Bütefisch CM, et al. Among authors: gambetti p. Neurology. 2000 Aug 22;55(4):517-22. doi: 10.1212/wnl.55.4.517. Neurology. 2000. PMID: 10953183

3

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

Capellari S, Vital C, Parchi P, Petersen RB, Ferrer X, Jarnier D, Pegoraro E, Gambetti P, Julien J. Capellari S, et al. Among authors: gambetti p. Neurology. 1997 Jul;49(1):133-41. doi: 10.1212/wnl.49.1.133. Neurology. 1997. PMID: 9222181

4

A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.

Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H. Hainfellner JA, et al. Among authors: gambetti p. Ann Neurol. 1999 Jun;45(6):812-6. Ann Neurol. 1999. PMID: 10360778

5

Familial mutations and the thermodynamic stability of the recombinant human prion protein.

Swietnicki W, Petersen RB, Gambetti P, Surewicz WK. Swietnicki W, et al. Among authors: gambetti p. J Biol Chem. 1998 Nov 20;273(47):31048-52. doi: 10.1074/jbc.273.47.31048. J Biol Chem. 1998. PMID: 9813003 Free article.

6

Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene.

Capellari S, Parchi P, Wolff BD, Campbell J, Atkinson R, Posey DM, Petersen RB, Gambetti P. Capellari S, et al. Among authors: gambetti p. Neurology. 2002 Nov 26;59(10):1628-30. doi: 10.1212/01.wnl.0000035533.86833.28. Neurology. 2002. PMID: 12451210

7

Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits.

Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P. Colucci M, et al. Among authors: gambetti p. J Neuropathol Exp Neurol. 2006 Jul;65(7):642-51. doi: 10.1097/01.jnen.0000228198.81797.4d. J Neuropathol Exp Neurol. 2006. PMID: 16825951

8

Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding.

Zaidi SI, Richardson SL, Capellari S, Song L, Smith MA, Ghetti B, Sy MS, Gambetti P, Petersen RB. Zaidi SI, et al. Among authors: gambetti p. J Alzheimers Dis. 2005 Apr;7(2):159-71; discussion 173-80. doi: 10.3233/jad-2005-7209. J Alzheimers Dis. 2005. PMID: 15851854

9

Redox metals and oxidative abnormalities in human prion diseases.

Petersen RB, Siedlak SL, Lee HG, Kim YS, Nunomura A, Tagliavini F, Ghetti B, Cras P, Moreira PI, Castellani RJ, Guentchev M, Budka H, Ironside JW, Gambetti P, Smith MA, Perry G. Petersen RB, et al. Among authors: gambetti p. Acta Neuropathol. 2005 Sep;110(3):232-8. doi: 10.1007/s00401-005-1034-4. Epub 2005 Aug 11. Acta Neuropathol. 2005. PMID: 16096758

10

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Gambetti P, et al. Brain Pathol. 1995 Jan;5(1):43-51. doi: 10.1111/j.1750-3639.1995.tb00576.x. Brain Pathol. 1995. PMID: 7767490 Review.

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