Pisciotta C - 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: pisciotta c. J Peripher Nerv Syst. 2014 Dec;19(4):292-8. doi: 10.1111/jns.12092. J Peripher Nerv Syst. 2014. PMID: 25429913

2

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: pisciotta c. Muscle Nerve. 2007 Dec;36(6):816-20. doi: 10.1002/mus.20872. Muscle Nerve. 2007. PMID: 17691102

3

Reliability of clinical outcome measures in Charcot-Marie-Tooth disease.

Solari A, Laurà M, Salsano E, Radice D, Pareyson D; CMT-TRIAAL Study Group. Solari A, et al. Neuromuscul Disord. 2008 Jan;18(1):19-26. doi: 10.1016/j.nmd.2007.09.006. Epub 2007 Oct 26. Neuromuscul Disord. 2008. PMID: 17964785 Clinical Trial.

4

Nine-year case history of monofocal motor neuropathy.

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

5

Case of acute motor conduction block neuropathy (AMCBN).

Manganelli F, Pisciotta C, Iodice R, Calandro S, Dubbioso R, Ranieri A, Santoro L. Manganelli F, et al. Among authors: pisciotta c. Muscle Nerve. 2009 Feb;39(2):224-6. doi: 10.1002/mus.21219. Muscle Nerve. 2009. PMID: 19145655

6

Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease.

Manganelli F, Vitale C, Santangelo G, Pisciotta C, Iodice R, Cozzolino A, Dubbioso R, Picillo M, Barone P, Santoro L. Manganelli F, et al. Among authors: pisciotta c. Brain. 2009 Sep;132(Pt 9):2350-5. doi: 10.1093/brain/awp166. Epub 2009 Jul 7. Brain. 2009. PMID: 19584099 Free PMC article.

7

Two families with novel PMP22 point mutations: genotype-phenotype correlation.

Pisciotta C, Manganelli F, Iodice R, Bellone E, Geroldi A, Volpi N, Mandich P, Santoro L. Pisciotta C, et al. J Peripher Nerv Syst. 2009 Sep;14(3):208-12. doi: 10.1111/j.1529-8027.2009.00235.x. J Peripher Nerv Syst. 2009. PMID: 19909487 No abstract available.

8

Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability.

Santoro L, Breedveld GJ, Manganelli F, Iodice R, Pisciotta C, Nolano M, Punzo F, Quarantelli M, Pappatà S, Di Fonzo A, Oostra BA, Bonifati V. Santoro L, et al. Among authors: pisciotta c. Neurogenetics. 2011 Feb;12(1):33-9. doi: 10.1007/s10048-010-0259-0. Epub 2010 Sep 21. Neurogenetics. 2011. PMID: 20853184 Free PMC article.

9

Electrophysiological characterisation in hereditary spastic paraplegia type 5.

Manganelli F, Pisciotta C, Dubbioso R, Iodice R, Criscuolo C, Ruggiero L, De Michele G, Santoro L. Manganelli F, et al. Among authors: pisciotta c. Clin Neurophysiol. 2011 Apr;122(4):819-22. doi: 10.1016/j.clinph.2010.10.025. Epub 2010 Dec 15. Clin Neurophysiol. 2011. PMID: 21111673

10

Thermosensitive hereditary neuropathy with liability to pressure palsy.

Pisciotta C, Manganelli F, Dubbioso R, Ruggiero L, Iodice R, Santoro L. Pisciotta C, et al. Muscle Nerve. 2011 Mar;43(3):448-9. doi: 10.1002/mus.21921. Muscle Nerve. 2011. PMID: 21321961 No abstract available.

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