Pastorello E - Search Results

1

Prevalence of inherited ataxias in the province of Padua, Italy.

Zortea M, Armani M, Pastorello E, Nunez GF, Lombardi S, Tonello S, Rigoni MT, Zuliani L, Mostacciuolo ML, Gellera C, Di Donato S, Trevisan CP. Zortea M, et al. Among authors: pastorello e. Neuroepidemiology. 2004 Nov-Dec;23(6):275-80. doi: 10.1159/000080092. Epub 2004 Aug 5. Neuroepidemiology. 2004. PMID: 15297793

2

Ataxia and congenital muscular dystrophy: the follow-up of a new specific phenotype.

Trevisan CP, Pastorello E, Tonello S, Armani M, Rigoni MT, Tormene AP, Freda MP, Zortea M, Lombardi S. Trevisan CP, et al. Among authors: pastorello e. Brain Dev. 2001 Mar;23(2):108-14. doi: 10.1016/s0387-7604(01)00187-5. Brain Dev. 2001. PMID: 11248459

3

Friedreich's ataxia: clinical heterogeneity in two sisters.

Armani M, Zortea M, Pastorello E, Lombardi S, Tonello S, Zuliani L, Rigoni MT, Trevisan CP. Armani M, et al. Among authors: pastorello e. Neurol Sci. 2006 Jun;27(2):140-2. doi: 10.1007/s10072-006-0617-8. Neurol Sci. 2006. PMID: 16816915

4

Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample.

Mostacciuolo ML, Pastorello E, Vazza G, Miorin M, Angelini C, Tomelleri G, Galluzzi G, Trevisan CP. Mostacciuolo ML, et al. Among authors: pastorello e. Clin Genet. 2009 Jun;75(6):550-5. doi: 10.1111/j.1399-0004.2009.01158.x. Epub 2009 Mar 23. Clin Genet. 2009. PMID: 19320656

5

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

Pastorello E, Cao M, Trevisan CP. Pastorello E, et al. 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.

6

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: pastorello e. J Neurol. 1999 Mar;246(3):186-92. doi: 10.1007/s004150050332. J Neurol. 1999. PMID: 10323316

7

Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function.

Trevisan CP, Pastorello E, Ermani M, Angelini C, Tomelleri G, Tonin P, Mongini T, Palmucci L, Galluzzi G, Tupler RG, Marioni G, Rimini A. Trevisan CP, et al. Among authors: pastorello e. Audiol Neurootol. 2008;13(1):1-6. doi: 10.1159/000107431. Epub 2007 Aug 22. Audiol Neurootol. 2008. PMID: 17715463

8

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. Among authors: pastorello e. Eur Neurol. 2006;56(1):1-5. doi: 10.1159/000094248. Epub 2006 Jun 27. Eur Neurol. 2006. PMID: 16804309

9

Alterations of the retino-cortical conduction in patients affected by classical congenital muscular dystrophy (CI-CMD) with merosin deficiency.

Tormene AP, Trevisan C, Martinello F, Riva C, Pastorello E. Tormene AP, et al. Among authors: pastorello e. Doc Ophthalmol. 1999;98(2):127-38. doi: 10.1023/a:1002093705611. Doc Ophthalmol. 1999. PMID: 10946999

10

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. Among authors: pastorello e. Eur J Neurol. 2008 Dec;15(12):1353-8. doi: 10.1111/j.1468-1331.2008.02314.x. Eur J Neurol. 2008. PMID: 19049553

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