Trevisan CP - Search Results

1

Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy.

Martinello F, Piazza A, Pastorello E, Angelini C, Trevisan CP. Martinello F, et al. Among authors: trevisan cp. J Neurol. 1999 Mar;246(3):186-92. doi: 10.1007/s004150050332. J Neurol. 1999. PMID: 10323316

2

Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia.

Trevisan CP, Pastorello E, Armani M, Angelini C, Nante G, Tomelleri G, Tonin P, Mongini T, Palmucci L, Galluzzi G, Tupler RG, Barchitta A. Trevisan CP, et al. Eur Neurol. 2006;56(1):1-5. doi: 10.1159/000094248. Epub 2006 Jun 27. Eur Neurol. 2006. PMID: 16804309

3

Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy.

Pastorello E, Cao M, Trevisan CP. Pastorello E, et al. Among authors: trevisan cp. Clin Neurol Neurosurg. 2012 Apr;114(3):230-4. doi: 10.1016/j.clineuro.2011.10.022. Epub 2011 Nov 12. Clin Neurol Neurosurg. 2012. PMID: 22079131 Free PMC article.

4

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up.

Trevisan CP, Martinello F, Ferruzza E, Angelini C. Trevisan CP, et al. Eur Neurol. 1995;35(4):230-5. doi: 10.1159/000117134. Eur Neurol. 1995. PMID: 7671985

5

Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.

Trevisan CP, Martinello F, Ferruzza E, Fanin M, Chevallay M, Tomé FM. Trevisan CP, et al. Childs Nerv Syst. 1996 Oct;12(10):604-10. doi: 10.1007/BF00261655. Childs Nerv Syst. 1996. PMID: 8934020

6

Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy.

Martinello F, Angelini C, Trevisan CP. Martinello F, et al. Among authors: trevisan cp. Eur Neurol. 1998 Jul;40(1):37-45. doi: 10.1159/000007954. Eur Neurol. 1998. PMID: 9693231

7

A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.

Pegoraro E, Fanin M, Trevisan CP, Angelini C, Hoffman EP. Pegoraro E, et al. Among authors: trevisan cp. Neurology. 2000 Oct 24;55(8):1128-34. doi: 10.1212/wnl.55.8.1128. Neurology. 2000. PMID: 11071490

8

Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.

Trevisan CP, Pastorello E, Tomelleri G, Vercelli L, Bruno C, Scapolan S, Siciliano G, Comacchio F. Trevisan CP, et al. Eur J Neurol. 2008 Dec;15(12):1353-8. doi: 10.1111/j.1468-1331.2008.02314.x. Eur J Neurol. 2008. PMID: 19049553

9

Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2.

Romeo V, Pegoraro E, Ferrati C, Squarzanti F, Sorarù G, Palmieri A, Zucchetta P, Antunovic L, Bonifazi E, Novelli G, Trevisan CP, Ermani M, Manara R, Angelini C. Romeo V, et al. Among authors: trevisan cp. J Neurol. 2010 Aug;257(8):1246-55. doi: 10.1007/s00415-010-5498-3. Epub 2010 Mar 11. J Neurol. 2010. PMID: 20221771

10

Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2).

Salvatori S, Furlan S, Fanin M, Picard A, Pastorello E, Romeo V, Trevisan CP, Angelini C. Salvatori S, et al. Among authors: trevisan cp. Neurol Sci. 2009 Jun;30(3):185-92. doi: 10.1007/s10072-009-0048-4. Epub 2009 Mar 27. Neurol Sci. 2009. PMID: 19326042

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