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2021 1
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Page 1
Ultrastructural changes in LGMD1F.
Cenacchi G, Peterle E, Fanin M, Papa V, Salaroli R, Angelini C. Cenacchi G, et al. Among authors: peterle e. Neuropathology. 2013 Jun;33(3):276-80. doi: 10.1111/neup.12003. Epub 2012 Dec 21. Neuropathology. 2013. PMID: 23279333
Incomplete penetrance in limb-girdle muscular dystrophy type 1F.
Fanin M, Peterle E, Fritegotto C, Nascimbeni AC, Tasca E, Torella A, Nigro V, Angelini C. Fanin M, et al. Among authors: peterle e. Muscle Nerve. 2015 Aug;52(2):305-6. doi: 10.1002/mus.24539. Epub 2015 Jun 7. Muscle Nerve. 2015. PMID: 25487718 No abstract available.
Narrative Analysis of the Impact of COVID-19 on Patients with Chronic Obstructive Pulmonary Disease, Their Caregivers, and Healthcare Professionals in Italy.
Volpato E, Centanni S, Banfi P, D'Antonio S, Peterle E, Bugliaro F, Grattagliano I, Piraino A, Cavalieri L, Pennisi A, Danesi G, Santoiemma L, Marini MG. Volpato E, et al. Among authors: peterle e. Int J Chron Obstruct Pulmon Dis. 2021 Jul 24;16:2181-2201. doi: 10.2147/COPD.S312372. eCollection 2021. Int J Chron Obstruct Pulmon Dis. 2021. PMID: 34335023 Free PMC article.
Next-generation sequencing identifies transportin 3 as the causative gene for LGMD1F.
Torella A, Fanin M, Mutarelli M, Peterle E, Del Vecchio Blanco F, Rispoli R, Savarese M, Garofalo A, Piluso G, Morandi L, Ricci G, Siciliano G, Angelini C, Nigro V. Torella A, et al. Among authors: peterle e. PLoS One. 2013 May 7;8(5):e63536. doi: 10.1371/journal.pone.0063536. Print 2013. PLoS One. 2013. PMID: 23667635 Free PMC article.
Pilot trial of clenbuterol in spinal and bulbar muscular atrophy.
Querin G, D'Ascenzo C, Peterle E, Ermani M, Bello L, Melacini P, Morandi L, Mazzini L, Silani V, Raimondi M, Mandrioli J, Romito S, Angelini C, Pegoraro E, Sorarù G. Querin G, et al. Among authors: peterle e. Neurology. 2013 Jun 4;80(23):2095-8. doi: 10.1212/WNL.0b013e318295d766. Epub 2013 May 3. Neurology. 2013. PMID: 23645595 Clinical Trial.