Capellari S - Search Results

1

Gait disorders in fatal familial insomnia.

Cortelli P, Fabbri M, Calandra-Buonaura G, Capellari S, Tinuper P, Parchi P, Lugaresi E. Cortelli P, et al. Among authors: capellari s. Mov Disord. 2014 Mar;29(3):420-4. doi: 10.1002/mds.25786. Epub 2013 Dec 27. Mov Disord. 2014. PMID: 24375448

2

Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy.

Tinuper P, Plazzi G, Monari L, Sangiorgi S, Pellissier JF, Cerullo A, Provini F, Capellari S, Baruzzi A, Lugaresi E, et al. Tinuper P, et al. Among authors: capellari s. Epilepsia. 1994 Mar-Apr;35(2):332-5. doi: 10.1111/j.1528-1157.1994.tb02440.x. Epilepsia. 1994. PMID: 7908874

3

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: capellari s. Nat Med. 1997 Sep;3(9):1009-15. doi: 10.1038/nm0997-1009. Nat Med. 1997. PMID: 9288728

4

Molecular pathology of fatal familial insomnia.

Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Parchi P, et al. Among authors: capellari s. Brain Pathol. 1998 Jul;8(3):539-48. doi: 10.1111/j.1750-3639.1998.tb00176.x. Brain Pathol. 1998. PMID: 9669705 Free PMC article. Review.

5

A subtype of sporadic prion disease mimicking fatal familial insomnia.

Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P. Parchi P, et al. Among authors: capellari s. Neurology. 1999 Jun 10;52(9):1757-63. doi: 10.1212/wnl.52.9.1757. Neurology. 1999. PMID: 10371520

6

Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.

Parchi P, Capellari S, Gambetti P. Parchi P, et al. Among authors: capellari s. Microsc Res Tech. 2000 Jul 1;50(1):16-25. doi: 10.1002/1097-0029(20000701)50:1<16::AID-JEMT4>3.0.CO;2-Y. Microsc Res Tech. 2000. PMID: 10871544 Review.

7

Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease.

Taratuto AL, Piccardo P, Reich EG, Chen SG, Sevlever G, Schultz M, Luzzi AA, Rugiero M, Abecasis G, Endelman M, Garcia AM, Capellari S, Xie Z, Lugaresi E, Gambetti P, Dlouhy SR, Ghetti B. Taratuto AL, et al. Among authors: capellari s. Neurology. 2002 Feb 12;58(3):362-7. doi: 10.1212/wnl.58.3.362. Neurology. 2002. PMID: 11839833

8

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: capellari s. J Biol Chem. 2004 Apr 16;279(16):16797-804. doi: 10.1074/jbc.M313220200. Epub 2004 Jan 29. J Biol Chem. 2004. PMID: 14754888 Free article.

9

Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.

Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P. Capellari S, et al. Neurology. 2005 Mar 8;64(5):905-7. doi: 10.1212/01.WNL.0000152837.82388.DE. Neurology. 2005. PMID: 15753435

10

MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome.

Magherini A, Pentore R, Galassi G, Stucchi CM, Capellari S, Parchi P. Magherini A, et al. Among authors: capellari s. Mov Disord. 2007 Apr 30;22(6):898-9. doi: 10.1002/mds.21426. Mov Disord. 2007. PMID: 17393534 No abstract available.

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