Pegoraro V - Search Results

1

A new family with transportinopathy: increased clinical heterogeneity.

Angelini C, Marozzo R, Pinzan E, Pegoraro V, Molnar MJ, Torella A, Nigro V. Angelini C, et al. Among authors: pegoraro v. Ther Adv Neurol Disord. 2019 Jun 9;12:1756286419850433. doi: 10.1177/1756286419850433. eCollection 2019. Ther Adv Neurol Disord. 2019. PMID: 31217819 Free PMC article.

2

Micro-RNAs in ALS muscle: Differences in gender, age at onset and disease duration.

Pegoraro V, Merico A, Angelini C. Pegoraro V, et al. J Neurol Sci. 2017 Sep 15;380:58-63. doi: 10.1016/j.jns.2017.07.008. Epub 2017 Jul 6. J Neurol Sci. 2017. PMID: 28870590 Free PMC article.

3

MiRNAs as biomarkers of phenotype in neutral lipid storage disease with myopathy.

Pegoraro V, Missaglia S, Marozzo R, Tavian D, Angelini C. Pegoraro V, et al. Muscle Nerve. 2020 Feb;61(2):253-257. doi: 10.1002/mus.26761. Epub 2019 Nov 29. Muscle Nerve. 2020. PMID: 31729045 Free PMC article.

4

MiRNAs, Myostatin, and Muscle MRI Imaging as Biomarkers of Clinical Features in Becker Muscular Dystrophy.

Marozzo R, Pegoraro V, Angelini C. Marozzo R, et al. Among authors: pegoraro v. Diagnostics (Basel). 2020 Sep 18;10(9):713. doi: 10.3390/diagnostics10090713. Diagnostics (Basel). 2020. PMID: 32961888 Free PMC article.

5

Circulating miR-206 as a Biomarker for Patients Affected by Severe Limb Girdle Muscle Dystrophies.

Pegoraro V, Angelini C. Pegoraro V, et al. Genes (Basel). 2021 Jan 12;12(1):85. doi: 10.3390/genes12010085. Genes (Basel). 2021. PMID: 33445560 Free PMC article.

6

Review: Danon disease: Review of natural history and recent advances.

Cenacchi G, Papa V, Pegoraro V, Marozzo R, Fanin M, Angelini C. Cenacchi G, et al. Among authors: pegoraro v. Neuropathol Appl Neurobiol. 2020 Jun;46(4):303-322. doi: 10.1111/nan.12587. Epub 2019 Nov 25. Neuropathol Appl Neurobiol. 2020. PMID: 31698507 Review.

7

Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review.

Di Stadio A, Pegoraro V, Giaretta L, Dipietro L, Marozzo R, Angelini C. Di Stadio A, et al. Among authors: pegoraro v. Orphanet J Rare Dis. 2018 Feb 21;13(1):35. doi: 10.1186/s13023-018-0770-1. Orphanet J Rare Dis. 2018. PMID: 29466997 Free PMC article.

8

Current and emerging therapies in Becker muscular dystrophy (BMD).

Angelini C, Marozzo R, Pegoraro V. Angelini C, et al. Among authors: pegoraro v. Acta Myol. 2019 Sep 1;38(3):172-179. eCollection 2019 Sep. Acta Myol. 2019. PMID: 31788661 Free PMC article. Review.

9

Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients.

Missaglia S, Pegoraro V, Marozzo R, Tavian D, Angelini C. Missaglia S, et al. Among authors: pegoraro v. Eur J Transl Myol. 2020 Apr 1;30(1):8880. doi: 10.4081/ejtm.2019.8880. eCollection 2020 Apr 7. Eur J Transl Myol. 2020. PMID: 32499892 Free PMC article.

10

Diagnostic challenges in metabolic myopathies.

Angelini C, Marozzo R, Pegoraro V, Sacconi S. Angelini C, et al. Among authors: pegoraro v. Expert Rev Neurother. 2020 Dec;20(12):1287-1298. doi: 10.1080/14737175.2020.1825943. Epub 2020 Oct 4. Expert Rev Neurother. 2020. PMID: 32941087 Review.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

93 results

Search Page

Filters