Capellari S - Search Results

1

Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease.

Donadio V, Incensi A, Leta V, Giannoccaro MP, Scaglione C, Martinelli P, Capellari S, Avoni P, Baruzzi A, Liguori R. Donadio V, et al. Among authors: capellari s. Neurology. 2014 Apr 15;82(15):1362-9. doi: 10.1212/WNL.0000000000000316. Epub 2014 Mar 14. Neurology. 2014. PMID: 24634456

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

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.

4

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

5

Sporadic fatal insomnia in a fatal familial insomnia pedigree.

Capellari S, Parchi P, Cortelli P, Avoni P, Casadei GP, Bini C, Baruzzi A, Lugaresi E, Pocchiari M, Gambetti P, Montagna P. Capellari S, et al. Neurology. 2008 Mar 11;70(11):884-5. doi: 10.1212/01.wnl.0000287140.94379.52. Neurology. 2008. PMID: 18332347 No abstract available.

6

Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.

Rizzo G, Martinelli P, Manners D, Scaglione C, Tonon C, Cortelli P, Malucelli E, Capellari S, Testa C, Parchi P, Montagna P, Barbiroli B, Lodi R. Rizzo G, et al. Among authors: capellari s. Brain. 2008 Oct;131(Pt 10):2690-700. doi: 10.1093/brain/awn195. Epub 2008 Sep 26. Brain. 2008. PMID: 18819991

7

Benign tremulous parkinsonism in a patient with dardarin mutation.

Rizzo G, Marconi S, Capellari S, Scaglione C, Martinelli P. Rizzo G, et al. Among authors: capellari s. Mov Disord. 2009 Jul 15;24(9):1399-401. doi: 10.1002/mds.22544. Mov Disord. 2009. PMID: 19373934 No abstract available.

8

A case of fatal familial insomnia in Africa.

Baldin E, Capellari S, Provini F, Corrado P, Liguori R, Parchi P, Montagna P, Cortelli P. Baldin E, et al. Among authors: capellari s. J Neurol. 2009 Oct;256(10):1778-9. doi: 10.1007/s00415-009-5205-4. Epub 2009 Jun 14. J Neurol. 2009. PMID: 19526349 No abstract available.

9

The RET51/FKBP52 complex and its involvement in Parkinson disease.

Fusco D, Vargiolu M, Vidone M, Mariani E, Pennisi LF, Bonora E, Capellari S, Dirnberger D, Baumeister R, Martinelli P, Romeo G. Fusco D, et al. Among authors: capellari s. Hum Mol Genet. 2010 Jul 15;19(14):2804-16. doi: 10.1093/hmg/ddq181. Epub 2010 May 4. Hum Mol Genet. 2010. PMID: 20442138

10

Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy.

Guaraldi P, Donadio V, Capellari S, Contin M, Casadio MC, Montagna P, Liguori R, Cortelli P. Guaraldi P, et al. Among authors: capellari s. Auton Neurosci. 2011 Jan 20;159(1-2):123-6. doi: 10.1016/j.autneu.2010.07.011. Epub 2010 Aug 16. Auton Neurosci. 2011. PMID: 20719577

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