Manganelli F - Search Results

1

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

2

A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family.

Santoro L, Barbieri F, Crisci C, Gasparo Rippa P, Manganelli F. Santoro L, et al. Among authors: manganelli f. J Neurol. 1998 Apr;245(4):240-4. doi: 10.1007/s004150050213. J Neurol. 1998. PMID: 9591228 No abstract available.

3

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

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

Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome.

Santoro L, Manganelli F, Bruno R, Nolano M, Provitera V, Barbieri F. Santoro L, et al. Among authors: manganelli f. Eur J Neurol. 2006 Jan;13(1):99-102. doi: 10.1111/j.1468-1331.2006.01117.x. Eur J Neurol. 2006. PMID: 16420405 No abstract available.

10

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.

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