Manganelli F - Search Results

1

Telemedicine application to headache: a critical review.

Spina E, Tedeschi G, Russo A, Trojsi F, Iodice R, Tozza S, Iovino A, Iodice F, Abbadessa G, di Lorenzo F, Miele G, Maida E, Cerullo G, Sparaco M, Silvestro M, Leocani L, Bonavita S, Manganelli F, Lavorgna L; Digital Technologies, Web and Social Media Study Group of the Italian Society of Neurology (SIN). Spina E, et al. Among authors: manganelli f. Neurol Sci. 2022 Jun;43(6):3795-3801. doi: 10.1007/s10072-022-05910-6. Epub 2022 Jan 24. Neurol Sci. 2022. PMID: 35075575 Free PMC article. Review.

2

Nine-year case history of monofocal motor neuropathy.

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

3

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. Muscle Nerve. 2009 Feb;39(2):224-6. doi: 10.1002/mus.21219. Muscle Nerve. 2009. PMID: 19145655

4

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. Brain. 2009 Sep;132(Pt 9):2350-5. doi: 10.1093/brain/awp166. Epub 2009 Jul 7. Brain. 2009. PMID: 19584099 Free PMC article.

5

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: manganelli f. 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.

6

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. 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

7

A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.

Santoro L, Manganelli F, Fortunato MR, Soldovieri MV, Ambrosino P, Iodice R, Pisciotta C, Tessa A, Santorelli F, Taglialatela M. Santoro L, et al. Among authors: manganelli f. Cephalalgia. 2011 May;31(7):808-19. doi: 10.1177/0333102411399351. Epub 2011 Mar 11. Cephalalgia. 2011. PMID: 21398422

8

Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy.

Manganelli F, Dubbioso R, Nolano M, Iodice R, Pisciotta C, Provitera V, Ruggiero L, Serlenga L, Barbieri F, Santoro L. Manganelli F, et al. Arch Neurol. 2011 Apr;68(4):504-7. doi: 10.1001/archneurol.2011.60. Arch Neurol. 2011. PMID: 21482929

9

Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy.

Dubbioso R, Moretta P, Manganelli F, Fiorillo C, Iodice R, Trojano L, Santoro L. Dubbioso R, et al. Among authors: manganelli f. J Neurol. 2012 May;259(5):833-7. doi: 10.1007/s00415-011-6255-y. Epub 2011 Sep 29. J Neurol. 2012. PMID: 21956377

10

Autonomic nervous system involvement in a new CMT2B family.

Manganelli F, Pisciotta C, Provitera V, Taioli F, Iodice R, Topa A, Fabrizi GM, Nolano M, Santoro L. Manganelli F, et al. J Peripher Nerv Syst. 2012 Sep;17(3):361-4. doi: 10.1111/j.1529-8027.2012.00415.x. J Peripher Nerv Syst. 2012. PMID: 22971099

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