Manganelli F - Search Results

1

Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy.

Tozza S, Palumbo G, Severi D, Iovino A, Spina E, Aruta F, Cassano E, Iodice R, Dubbioso R, Ruggiero L, Nolano M, Santoro L, Manganelli F. Tozza S, et al. Among authors: manganelli f. Neurol Sci. 2024 Apr;45(4):1685-1689. doi: 10.1007/s10072-023-07140-w. Epub 2023 Oct 23. Neurol Sci. 2024. PMID: 37870643 Free PMC article.

2

Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the disease.

Santoro L, Perretti A, Lanzillo B, Coppola G, De Joanna G, Manganelli F, Cocozza S, De Michele G, Filla A, Caruso G. Santoro L, et al. Among authors: manganelli f. Clin Neurophysiol. 2000 Jun;111(6):1023-30. doi: 10.1016/s1388-2457(00)00290-x. Clin Neurophysiol. 2000. PMID: 10825709

3

Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family.

Santoro L, Manganelli F, Di Maio L, Barbieri F, Carella M, D'Adamo P, Casari G. Santoro L, et al. Among authors: manganelli f. Neuromuscul Disord. 2002 May;12(4):399-404. doi: 10.1016/s0960-8966(01)00305-4. Neuromuscul Disord. 2002. PMID: 12062259

4

Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis.

Del Giudice E, Savoldi G, Notarangelo LD, Di Benedetto L, Manganelli F, Bruzzese E, Romano A, Santoro L. Del Giudice E, et al. Among authors: manganelli f. Acta Paediatr. 2003;92(3):398-401. Acta Paediatr. 2003. PMID: 12725560

5

Distal hypoglycemic neuropathy. An insulinoma-associated case, misdiagnosed as temporal lobe epilepsy.

Striano S, Striano P, Manganelli F, Boccella P, Bruno R, Santoro L, Percopo V. Striano S, et al. Among authors: manganelli f. Neurophysiol Clin. 2003 Nov;33(5):223-7. doi: 10.1016/j.neucli.2003.08.001. Neurophysiol Clin. 2003. PMID: 14672823

6

A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease.

Santoro L, Manganelli F, Di Maria E, Bordo D, Cassandrini D, Ajmar F, Mandich P, Bellone E. Santoro L, et al. Among authors: manganelli f. J Neurol Neurosurg Psychiatry. 2004 Feb;75(2):262-5. J Neurol Neurosurg Psychiatry. 2004. PMID: 14742601 Free PMC article.

7

Post-exercise facilitation and depression of motor evoked potentials to transcranial magnetic stimulation: a study in multiple sclerosis.

Perretti A, Balbi P, Orefice G, Trojano L, Marcantonio L, Brescia-Morra V, Ascione S, Manganelli F, Conte G, Santoro L. Perretti A, et al. Among authors: manganelli f. Clin Neurophysiol. 2004 Sep;115(9):2128-33. doi: 10.1016/j.clinph.2004.03.028. Clin Neurophysiol. 2004. PMID: 15294215

8

Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family.

Ragno M, Perretti AC, Castaldo I, Scarcella M, Acciarri S, Manganelli F, Santoro L. Ragno M, et al. Among authors: manganelli f. Neurol Sci. 2005 Jun;26(2):67-71. doi: 10.1007/s10072-005-0438-1. Neurol Sci. 2005. PMID: 15995822

9

Prevalence and characteristics of peripheral neuropathy in hepatitis C virus population.

Santoro L, Manganelli F, Briani C, Giannini F, Benedetti L, Vitelli E, Mazzeo A, Beghi E; HCV Peripheral Nerve Study Group. Santoro L, et al. Among authors: manganelli f. J Neurol Neurosurg Psychiatry. 2006 May;77(5):626-9. doi: 10.1136/jnnp.2005.081570. Epub 2006 Feb 7. J Neurol Neurosurg Psychiatry. 2006. PMID: 16464900 Free PMC article.

10

Electrophysiologic characterization in spinocerebellar ataxia 17.

Manganelli F, Perretti A, Nolano M, Lanzillo B, Bruni AC, De Michele G, Filla A, Santoro L. Manganelli F, et al. Neurology. 2006 Mar 28;66(6):932-4. doi: 10.1212/01.wnl.0000203514.92781.fd. Neurology. 2006. PMID: 16567717

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