Santoro L - Search Results

1

Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population.

Manganelli F, Tozza S, Pisciotta C, Bellone E, Iodice R, Nolano M, Geroldi A, Capponi S, Mandich P, Santoro L. Manganelli F, et al. Among authors: santoro l. J Peripher Nerv Syst. 2014 Dec;19(4):292-8. doi: 10.1111/jns.12092. J Peripher Nerv Syst. 2014. PMID: 25429913

2

Blockade of glutamate mGlu5 receptors in a rat model of neuropathic pain prevents early over-expression of pro-apoptotic genes and morphological changes in dorsal horn lamina II.

de Novellis V, Siniscalco D, Galderisi U, Fuccio C, Nolano M, Santoro L, Cascino A, Roth KA, Rossi F, Maione S. de Novellis V, et al. Among authors: santoro l. Neuropharmacology. 2004 Mar;46(4):468-79. doi: 10.1016/j.neuropharm.2003.10.014. Neuropharmacology. 2004. PMID: 14975670

3

Skin sympathetic adrenergic innervation: an immunofluorescence confocal study.

Donadio V, Nolano M, Provitera V, Stancanelli A, Lullo F, Liguori R, Santoro L. Donadio V, et al. Among authors: santoro l. Ann Neurol. 2006 Feb;59(2):376-81. doi: 10.1002/ana.20769. Ann Neurol. 2006. PMID: 16437571

4

Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.

Salvatore E, Varrone A, Sansone V, Nolano M, Bruni AC, De Rosa A, Santoro L, Pappatà S, Filla A, De Michele G. Salvatore E, et al. Among authors: santoro l. Mov Disord. 2006 Jun;21(6):872-5. doi: 10.1002/mds.20827. Mov Disord. 2006. PMID: 16532453

5

GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features.

Biancheri R, Zara F, Striano P, Pedemonte M, Cassandrini D, Stringara S, Manganelli F, Santoro L, Schenone A, Bellone E, Minetti C. Biancheri R, et al. Among authors: santoro l. J Neurol. 2006 Sep;253(9):1234-5. doi: 10.1007/s00415-006-0149-4. Epub 2006 Apr 10. J Neurol. 2006. PMID: 16607474 No abstract available.

6

Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects.

Nolano M, Provitera V, Perretti A, Stancanelli A, Saltalamacchia AM, Donadio V, Manganelli F, Lanzillo B, Santoro L. Nolano M, et al. Among authors: santoro l. Brain. 2006 Aug;129(Pt 8):2119-31. doi: 10.1093/brain/awl175. Epub 2006 Jul 12. Brain. 2006. PMID: 16837483

7

Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease).

Manganelli F, Iodice V, Provitera V, Pisciotta C, Nolano M, Perretti A, Santoro L. Manganelli F, et al. Among authors: santoro l. Muscle Nerve. 2007 Dec;36(6):816-20. doi: 10.1002/mus.20872. Muscle Nerve. 2007. PMID: 17691102

8

Motor cortex cholinergic dysfunction in CADASIL: a transcranial magnetic demonstration.

Manganelli F, Ragno M, Cacchiò G, Iodice V, Trojano L, Silvaggio F, Scarcella M, Grazioli M, Santoro L, Perretti A. Manganelli F, et al. Among authors: santoro l. Clin Neurophysiol. 2008 Feb;119(2):351-5. doi: 10.1016/j.clinph.2007.10.011. Epub 2007 Dec 11. Clin Neurophysiol. 2008. PMID: 18065265

9

Familial aggregation of white matter lesions in myotonic dystrophy type 1.

Di Costanzo A, Santoro L, de Cristofaro M, Manganelli F, Di Salle F, Tedeschi G. Di Costanzo A, et al. Among authors: santoro l. Neuromuscul Disord. 2008 Apr;18(4):299-305. doi: 10.1016/j.nmd.2008.01.008. Epub 2008 Mar 11. Neuromuscul Disord. 2008. PMID: 18337099

10

Nine-year case history of monofocal motor neuropathy.

Manganelli F, Pisciotta C, Iodice R, Calandro S, Santoro L. Manganelli F, et al. Among authors: santoro l. Muscle Nerve. 2008 Jul;38(1):927-9. doi: 10.1002/mus.21005. Muscle Nerve. 2008. PMID: 18508346

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