Gambetti P - Search Results

1

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H. Parchi P, et al. Among authors: gambetti p. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888

2

Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.

Gambetti P, Parchi P, Chen SG. Gambetti P, et al. Clin Lab Med. 2003 Mar;23(1):43-64. doi: 10.1016/s0272-2712(02)00065-3. Clin Lab Med. 2003. PMID: 12733424 Review.

3

Classification of sporadic Creutzfeldt-Jakob disease revisited.

Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P. Cali I, et al. Among authors: gambetti p. Brain. 2006 Sep;129(Pt 9):2266-77. doi: 10.1093/brain/awl224. Brain. 2006. PMID: 16923954

In one classification proposed by Parchi et al., [Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I , Budka H , Kopp N , Piccardo P , Poser S , Rojiani A , Streichemberger N , Julien J , Vital C , Ghetti B , Gambetti P …

In one classification proposed by Parchi et al., [Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I …

4

Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.

Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P. Baiardi S, et al. Among authors: gambetti p. Acta Neuropathol. 2021 Oct;142(4):707-728. doi: 10.1007/s00401-021-02350-y. Epub 2021 Jul 29. Acta Neuropathol. 2021. PMID: 34324063 Free PMC article.

5

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.

6

Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies.

Castellani R, Parchi P, Stahl J, Capellari S, Cohen M, Gambetti P. Castellani R, et al. Among authors: gambetti p. Neurology. 1996 Jun;46(6):1690-3. doi: 10.1212/wnl.46.6.1690. Neurology. 1996. PMID: 8649571

7

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. Parchi P, et al. Among authors: gambetti p. Ann Neurol. 1996 Jun;39(6):767-78. doi: 10.1002/ana.410390613. Ann Neurol. 1996. PMID: 8651649

8

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

9

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. Chen SG, et al. Among authors: gambetti p. Nat Med. 1997 Sep;3(9):1009-15. doi: 10.1038/nm0997-1009. Nat Med. 1997. PMID: 9288728

10

Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case.

Ghorayeb I, Series C, Parchi P, Sawan B, Guez S, Laplanche JL, Capellari S, Gambetti P, Vital C. Ghorayeb I, et al. Among authors: gambetti p. Neurology. 1998 Jul;51(1):271-4. doi: 10.1212/wnl.51.1.271. Neurology. 1998. PMID: 9674819

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