Pierelli F - Search Results

1

Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family.

Leonardi L, Ziccardi L, Marcotulli C, Rubegni A, Longobardi A, Serrao M, Storti E, Pierelli F, Tessa A, Parisi V, Santorelli FM, Carlo C. Leonardi L, et al. Among authors: pierelli f. J Neurol. 2016 Apr;263(4):781-3. doi: 10.1007/s00415-016-8066-7. Epub 2016 Feb 25. J Neurol. 2016. PMID: 26914923

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

Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance.

Di Gennaro G, Buzzi MG, Ciccarelli O, Santorelli FM, Pierelli F, Fortini D, D'Onofrio M, Costa A, Nappi G, Casali C. Di Gennaro G, et al. Among authors: pierelli f. Headache. 2000 Jul-Aug;40(7):568-71. doi: 10.1046/j.1526-4610.2000.00088.x. Headache. 2000. PMID: 10940095

4

A simple method for estimating conduction velocity of the spinothalamic tract in healthy humans.

Rossi P, Serrao M, Amabile G, Parisi L, Pierelli F, Pozzessere G. Rossi P, et al. Among authors: pierelli f. Clin Neurophysiol. 2000 Nov;111(11):1907-15. doi: 10.1016/s1388-2457(00)00442-9. Clin Neurophysiol. 2000. PMID: 11068222

5

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

6

Cutaneous afferents mediating the cutaneous silent period in the upper limbs: evidences for a role of low-threshold sensory fibres.

Serrao M, Parisi L, Pierelli F, Rossi P. Serrao M, et al. Among authors: pierelli f. Clin Neurophysiol. 2001 Nov;112(11):2007-14. doi: 10.1016/s1388-2457(01)00675-7. Clin Neurophysiol. 2001. PMID: 11682338

7

Estimation of the conduction velocity of sympathetic sudomotor C fibres in healthy subjects: study of sympathetic skin reflex.

Parisi L, Rossi P, Valente G, Fattapposta F, Mellina V, Martini A, Pierelli F, Serrao M. Parisi L, et al. Among authors: pierelli f. Funct Neurol. 2001 Jul-Sep;16(3):231-7. Funct Neurol. 2001. PMID: 11769868 Clinical Trial.

8

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.

9

Early visual function impairment in CADASIL.

Parisi V, Pierelli F, Fattapposta F, Bianco F, Parisi L, Restuccia R, Malandrini A, Ferrari M, Carrera P. Parisi V, et al. Among authors: pierelli f. Neurology. 2003 Jun 24;60(12):2008-10. doi: 10.1212/01.wnl.0000070411.13217.7e. Neurology. 2003. PMID: 12821756

10

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

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