Pierelli F - Search Results

1

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

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

Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1.

Di Fabio R, Marcotulli C, Tessa A, Leonardi L, Storti E, Pierelli F, Santorelli FM, Casali C. Di Fabio R, et al. Among authors: pierelli f. J Neurol. 2014 Apr;261(4):747-51. doi: 10.1007/s00415-014-7247-5. Epub 2014 Feb 12. J Neurol. 2014. PMID: 24519355

4

Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease.

Leonardi L, Marcotulli C, McFarland KN, Tessa A, DiFabio R, Santorelli FM, Pierelli F, Ashizawa T, Casali C. Leonardi L, et al. Among authors: pierelli f. J Neurol. 2014 Sep;261(9):1691-4. doi: 10.1007/s00415-014-7394-8. Epub 2014 Jun 17. J Neurol. 2014. PMID: 24935856 Free PMC article.

5

Early-onset optic neuropathy as initial clinical presentation in SPG7.

Marcotulli C, Leonardi L, Tessa A, De Negris AM, Cornia R, Pierallini A, Haggiag S, Pierelli F, Santorelli FM, Casali C. Marcotulli C, et al. Among authors: pierelli f. J Neurol. 2014 Sep;261(9):1820-1. doi: 10.1007/s00415-014-7432-6. Epub 2014 Jul 18. J Neurol. 2014. PMID: 25034272 No abstract available.

6

Acute optic neuropathy associated with a novel MFN2 mutation.

Leonardi L, Marcotulli C, Storti E, Tessa A, Serrao M, Parisi V, Santorelli FM, Pierelli F, Casali C. Leonardi L, et al. Among authors: pierelli f. J Neurol. 2015 Jul;262(7):1678-80. doi: 10.1007/s00415-015-7756-x. Epub 2015 May 10. J Neurol. 2015. PMID: 25957633

7

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.

8

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

9

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

10

Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs.

Di Lorenzo C, Pierelli F, Coppola G, Grieco GS, Rengo C, Ciccolella M, Magis D, Bolla M, Casali C, Santorelli FM, Schoenen J. Di Lorenzo C, et al. Among authors: pierelli f. Neurology. 2009 May 5;72(18):1588-94. doi: 10.1212/WNL.0b013e3181a41269. Neurology. 2009. PMID: 19414726 Clinical Trial.

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