Pierelli F - Search Results

1

15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias.

Arcuria G, Marcotulli C, Galasso C, Pierelli F, Casali C. Arcuria G, et al. Among authors: pierelli f. J Neurol. 2019 Jul;266(7):1611-1622. doi: 10.1007/s00415-019-09299-9. Epub 2019 Apr 6. J Neurol. 2019. PMID: 30955123

2

Multiple mtDNA deletions: clinical and molecular correlations.

Santorelli FM, De Joanna G, Casali C, Tessa A, Siciliano G, Amabile GA, Pierelli F, Vilarinho L, Santoro L. Santorelli FM, et al. Among authors: pierelli f. J Inherit Metab Dis. 2000 Mar;23(2):155-61. doi: 10.1023/a:1005617916260. J Inherit Metab Dis. 2000. PMID: 10801057

3

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family.

Casali C, Bonifati V, Santorelli FM, Casari G, Fortini D, Patrignani A, Fabbrini G, Carrozzo R, D'Amati G, Locuratolo N, Vanacore N, Damiano M, Pierallini A, Pierelli F, Amabile GA, Meco G. Casali C, et al. Among authors: pierelli f. Neurology. 2001 Mar 27;56(6):802-5. doi: 10.1212/wnl.56.6.802. Neurology. 2001. PMID: 11274324

4

Current insights into familial spastic paraparesis: new advances in an old disease.

Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F. Fortini D, et al. Among authors: pierelli f. Funct Neurol. 2003 Jan-Mar;18(1):43-9. Funct Neurol. 2003. PMID: 12760414 Review.

5

Unilateral facial pain associated with recurrence of malignant thymoma: a case report.

Rossi P, Borrello L, Malpezzi MG, Casali C, Pierelli F. Rossi P, et al. Among authors: pierelli f. Eur Neurol. 2003;50(1):56-7. doi: 10.1159/000070861. Eur Neurol. 2003. PMID: 12824715 No abstract available.

6

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.

Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM. Grieco GS, et al. Among authors: pierelli f. Neurology. 2004 Jan 13;62(1):103-6. doi: 10.1212/01.wnl.0000104491.66816.77. Neurology. 2004. PMID: 14718707

7

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

Criscuolo C, Chessa L, Di Giandomenico S, Mancini P, Saccà F, Grieco GS, Piane M, Barbieri F, De Michele G, Banfi S, Pierelli F, Rizzuto N, Santorelli FM, Gallosti L, Filla A, Casali C. Criscuolo C, et al. Among authors: pierelli f. Neurology. 2006 Apr 25;66(8):1207-10. doi: 10.1212/01.wnl.0000208402.10512.4a. Neurology. 2006. PMID: 16636238

8

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.

Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C. Cricchi F, et al. Among authors: pierelli f. J Neurol Sci. 2007 Mar 15;254(1-2):69-71. doi: 10.1016/j.jns.2007.01.008. Epub 2007 Feb 12. J Neurol Sci. 2007. PMID: 17292920

9

Shortened cortical silent period in facial muscles of patients with migraine.

Curra A, Pierelli F, Coppola G, Barbanti P, Buzzi MG, Galeotti F, Serrao M, Truini A, Casali C, Pauri F, Cruccu G. Curra A, et al. Among authors: pierelli f. Pain. 2007 Nov;132(1-2):124-31. doi: 10.1016/j.pain.2007.05.009. Epub 2007 Jun 14. Pain. 2007. PMID: 17574759

10

The wolframin His611Arg polymorphism influences medication overuse headache.

Di Lorenzo C, Sances G, Di Lorenzo G, Rengo C, Ghiotto N, Guaschino E, Perrotta A, Santorelli FM, Grieco GS, Troisi A, Siracusano A, Pierelli F, Nappi G, Casali C. Di Lorenzo C, et al. Among authors: pierelli f. Neurosci Lett. 2007 Sep 13;424(3):179-84. doi: 10.1016/j.neulet.2007.07.037. Epub 2007 Aug 6. Neurosci Lett. 2007. PMID: 17719176

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