Ferrarini M - Search Results

1

Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: Pitfalls and red flags.

Campagnolo M, Taioli F, Cacciavillani M, Ruiz M, Luigetti M, Salvalaggio A, Castellani F, Testi S, Ferrarini M, Cavallaro T, Gasparotti R, Fabrizi GM, Briani C. Campagnolo M, et al. Among authors: ferrarini m. J Peripher Nerv Syst. 2020 Mar;25(1):19-26. doi: 10.1111/jns.12362. Epub 2020 Jan 14. J Peripher Nerv Syst. 2020. PMID: 31919945

2

PMP22 related congenital hypomyelination neuropathy.

Fabrizi GM, Simonati A, Taioli F, Cavallaro T, Ferrarini M, Rigatelli F, Pini A, Mostacciuolo ML, Rizzuto N. Fabrizi GM, et al. Among authors: ferrarini m. J Neurol Neurosurg Psychiatry. 2001 Jan;70(1):123-6. doi: 10.1136/jnnp.70.1.123. J Neurol Neurosurg Psychiatry. 2001. PMID: 11118262 Free PMC article.

3

A somatic and germline mosaic mutation in MPZ/P(0) mimics recessive inheritance of CMT1B.

Fabrizi GM, Ferrarini M, Cavallaro T, Jarre L, Polo A, Rizzuto N. Fabrizi GM, et al. Among authors: ferrarini m. Neurology. 2001 Jul 10;57(1):101-5. doi: 10.1212/wnl.57.1.101. Neurology. 2001. PMID: 11445635

4

Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation.

Capasso M, Di Muzio A, Ferrarini M, De Angelis MV, Caporale CM, Lupo S, Cavallaro T, Fabrizi GM, Uncini A. Capasso M, et al. Among authors: ferrarini m. Clin Neurophysiol. 2004 Jan;115(1):64-70. doi: 10.1016/j.clinph.2003.08.024. Clin Neurophysiol. 2004. PMID: 14706470

5

Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E.

Fabrizi GM, Cavallaro T, Angiari C, Bertolasi L, Cabrini I, Ferrarini M, Rizzuto N. Fabrizi GM, et al. Among authors: ferrarini m. Neurology. 2004 Apr 27;62(8):1429-31. doi: 10.1212/01.wnl.0000120664.07186.3c. Neurology. 2004. PMID: 15111691

6

An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy.

Frigerio R, Fabrizi GM, Ferrarini M, Cavallaro T, Brighina L, Santoro P, Agostoni E, Cavaletti G, Rizzuto N, Ferrarese C. Frigerio R, et al. Among authors: ferrarini m. Amyloid. 2004 Jun;11(2):121-4. doi: 10.1080/13506120410001727767. Amyloid. 2004. PMID: 15478468

7

A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization.

Ferrarini M, Squintani G, Cavallaro T, Ferrari S, Rizzuto N, Fabrizi GM. Ferrarini M, et al. J Neurol Sci. 2007 Sep 15;260(1-2):219-24. doi: 10.1016/j.jns.2007.05.015. Epub 2007 Jun 18. J Neurol Sci. 2007. PMID: 17572444

8

Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease.

Fabrizi GM, Ferrarini M, Cavallaro T, Cabrini I, Cerini R, Bertolasi L, Rizzuto N. Fabrizi GM, et al. Among authors: ferrarini m. Neurology. 2007 Jul 17;69(3):291-5. doi: 10.1212/01.wnl.0000265820.51075.61. Neurology. 2007. PMID: 17636067

9

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study.

Mazzucco S, Anzola GP, Ferrarini M, Taioli F, Olivato S, Burlina AP, Fabrizi GM, Rizzuto N. Mazzucco S, et al. Among authors: ferrarini m. Eur Neurol. 2009;61(1):46-9. doi: 10.1159/000165350. Epub 2008 Oct 24. Eur Neurol. 2009. PMID: 18948701

10

Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs.

Luigetti M, Fabrizi GM, Madia F, Ferrarini M, Conte A, Delgrande A, Tonali PA, Sabatelli M. Luigetti M, et al. Among authors: ferrarini m. Muscle Nerve. 2010 Sep;42(3):448-51. doi: 10.1002/mus.21734. Muscle Nerve. 2010. PMID: 20806400

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