Fabrizi GM - Search Results

1

Are novel outcome measures for Charcot-Marie-Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study.

Pazzaglia C, Padua L, Pareyson D, Schenone A, Aiello A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Coraci D, Gemignani F, Vitetta F, Quattrone A, Mazzeo A, Russo M, Vita G; CMT-TRIAAL Group. Pazzaglia C, et al. Among authors: fabrizi gm. Neuromuscul Disord. 2019 Apr;29(4):310-316. doi: 10.1016/j.nmd.2019.01.009. Epub 2019 Feb 2. Neuromuscul Disord. 2019. PMID: 30926199

2

Neuronal intranuclear inclusion disease: polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case.

Malandrini A, Fabrizi GM, Cavallaro T, Zazzi M, Parrotta E, Romano L, Berti G, Villanova M, Guazzi GC. Malandrini A, et al. Among authors: fabrizi gm. Acta Neuropathol. 1996;91(2):215-8. doi: 10.1007/s004010050417. Acta Neuropathol. 1996. PMID: 8787158

3

Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases.

Fabrizi GM, Simonati A, Morbin M, Cavallaro T, Taioli F, Benedetti MD, Edomi P, Rizzuto N. Fabrizi GM, et al. Muscle Nerve. 1998 Jul;21(7):869-77. doi: 10.1002/(sici)1097-4598(199807)21:7<869::aid-mus4>3.0.co;2-4. Muscle Nerve. 1998. PMID: 9626246

4

Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome.

Fabrizi GM, Cavallaro T, Morbin M, Simonati A, Taioli F, Rizzuto N. Fabrizi GM, et al. J Neurol Neurosurg Psychiatry. 1999 Mar;66(3):386-9. doi: 10.1136/jnnp.66.3.386. J Neurol Neurosurg Psychiatry. 1999. PMID: 10084540 Free PMC article.

5

Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22.

Simonati A, Fabrizi GM, Pasquinelli A, Taioli F, Cavallaro T, Morbin M, Marcon G, Papini M, Rizzuto N. Simonati A, et al. Among authors: fabrizi gm. Neuromuscul Disord. 1999 Jun;9(4):257-61. doi: 10.1016/s0960-8966(99)00008-5. Neuromuscul Disord. 1999. PMID: 10399754

6

Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22.

Fabrizi GM, Cavallaro T, Taioli F, Orrico D, Morbin M, Simonati A, Rizzuto N. Fabrizi GM, et al. Neurology. 1999 Sep 11;53(4):846-51. doi: 10.1212/wnl.53.4.846. Neurology. 1999. PMID: 10489052

7

Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero.

Fabrizi GM, Taioli F, Cavallaro T, Rigatelli F, Simonati A, Mariani G, Perrone P, Rizzuto N. Fabrizi GM, et al. Acta Neuropathol. 2000 Sep;100(3):299-304. doi: 10.1007/s004019900175. Acta Neuropathol. 2000. PMID: 10965800

8

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. Neurology. 2001 Jul 10;57(1):101-5. doi: 10.1212/wnl.57.1.101. Neurology. 2001. PMID: 11445635

9

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: fabrizi gm. Clin Neurophysiol. 2004 Jan;115(1):64-70. doi: 10.1016/j.clinph.2003.08.024. Clin Neurophysiol. 2004. PMID: 14706470

10

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. Neurology. 2004 Apr 27;62(8):1429-31. doi: 10.1212/01.wnl.0000120664.07186.3c. Neurology. 2004. PMID: 15111691

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

170 results

Search Page