Peterle E - Search Results

1

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.

2

Old and new therapeutic developments in steroid treatment in Duchenne muscular dystrophy.

Angelini C, Peterle E. Angelini C, et al. Among authors: peterle e. Acta Myol. 2012 May;31(1):9-15. Acta Myol. 2012. PMID: 22655511 Free PMC article. Review.

3

Clinical phenotype, muscle MRI and muscle pathology of LGMD1F.

Peterle E, Fanin M, Semplicini C, Padilla JJ, Nigro V, Angelini C. Peterle E, et al. J Neurol. 2013 Aug;260(8):2033-41. doi: 10.1007/s00415-013-6931-1. Epub 2013 Apr 30. J Neurol. 2013. PMID: 23632945

4

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.

5

Dysferlinopathy course and sportive activity: clues for possible treatment.

Angelini C, Peterle E, Gaiani A, Bortolussi L, Borsato C. Angelini C, et al. Among authors: peterle e. Acta Myol. 2011 Oct;30(2):127-32. Acta Myol. 2011. PMID: 22106716 Free PMC article.

6

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.

7

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

8

Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases.

Filocamo M, Baldo C, Goldwurm S, Renieri A, Angelini C, Moggio M, Mora M, Merla G, Politano L, Garavaglia B, Casareto L, Bricarelli FD; Telethon Network of Genetic Biobanks Staff. Filocamo M, et al. Orphanet J Rare Dis. 2013 Aug 30;8:129. doi: 10.1186/1750-1172-8-129. Orphanet J Rare Dis. 2013. PMID: 24004821 Free PMC article.

9

An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps.

Fanin M, Benedicenti F, Fritegotto C, Nascimbeni AC, Peterle E, Stanzial F, Cristofoletti A, Castellan C, Angelini C. Fanin M, et al. Among authors: peterle e. Clin Genet. 2012 Dec;82(6):601-2. doi: 10.1111/j.1399-0004.2012.01873.x. Epub 2012 Apr 9. Clin Genet. 2012. PMID: 22486197 No abstract available.

10

Well-Established and Traditional Use of Vegetal Extracts as an Approach to the "Deep Roots" of Cough.

Pecoraro L, Peterle E, Dalla Benetta E, Piazza M, Chatziparasidis G, Kantar A. Pecoraro L, et al. Among authors: peterle e. Children (Basel). 2024 May 11;11(5):584. doi: 10.3390/children11050584. Children (Basel). 2024. PMID: 38790578 Free PMC article. Review.

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