Toscano A - Search Results

1

Impaired myocardial strain in early stage of Duchenne muscular dystrophy: its relation with age and motor performance.

Oreto L, Vita GL, Mandraffino G, Carerj S, Calabrò MP, Manganaro R, Cusmà-Piccione M, Todaro MC, Sframeli M, Cinquegrani M, Toscano A, Vita G, Messina S, Zito C. Oreto L, et al. Among authors: toscano a. Acta Myol. 2020 Dec 1;39(4):191-199. doi: 10.36185/2532-1900-022. eCollection 2020 Dec. Acta Myol. 2020. PMID: 33458574 Free PMC article.

2

Apoptosis and apoptosis-related proteins in thyroid myopathies.

Monici MC, Rodolico C, Toscano A, Messina S, Benvenga S, Messina C, Vita G. Monici MC, et al. Among authors: toscano a. Muscle Nerve. 2002 Sep;26(3):383-8. doi: 10.1002/mus.10212. Muscle Nerve. 2002. PMID: 12210368

3

Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data.

Di Leo R, Rodolico C, De Gregorio C, Recupero A, Coglitore S, Annesi G, Toscano A, Messina C, Vita G. Di Leo R, et al. Among authors: toscano a. Neuromuscul Disord. 2004 Feb;14(2):136-41. doi: 10.1016/j.nmd.2003.11.002. Neuromuscul Disord. 2004. PMID: 14733960

4

Axial myopathy in myasthenia: a misleading cause of dropped head.

Rodolico C, Messina S, Toscano A, Vita G, Gaeta M. Rodolico C, et al. Among authors: toscano a. Muscle Nerve. 2004 Feb;29(2):329-30. doi: 10.1002/mus.10543. Muscle Nerve. 2004. PMID: 14755502 No abstract available.

5

Oxidative stress in myotonic dystrophy type 1.

Toscano A, Messina S, Campo GM, Di Leo R, Musumeci O, Rodolico C, Aguennouz M, Annesi G, Messina C, Vita G. Toscano A, et al. Free Radic Res. 2005 Jul;39(7):771-6. doi: 10.1080/10715760500138932. Free Radic Res. 2005. PMID: 16036357

6

Diffuse metabolic changes in the brain of patients with familial amyloid polyneuropathy. A proton MRSI study.

Mazzeo A, Toscano A, Stromillo ML, Battaglini M, Messina C, Federico A, Vita G, De Stefano N. Mazzeo A, et al. Among authors: toscano a. J Neurol Sci. 2006 Jul 15;246(1-2):31-5. doi: 10.1016/j.jns.2006.01.017. Epub 2006 Mar 10. J Neurol Sci. 2006. PMID: 16530227

7

Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency.

Musumeci O, Aguennouz M, Comi GP, Rodolico C, Autunno M, Bordoni A, Baratta S, Taroni F, Vita G, Toscano A. Musumeci O, et al. Among authors: toscano a. Neuromuscul Disord. 2007 Dec;17(11-12):960-3. doi: 10.1016/j.nmd.2007.05.002. Epub 2007 Jul 24. Neuromuscul Disord. 2007. PMID: 17651973

8

Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathy.

Graceffa A, Russo M, Vita GL, Toscano A, Dattola R, Messina C, Vita G, Mazzeo A. Graceffa A, et al. Among authors: toscano a. Neuromuscul Disord. 2009 Jan;19(1):44-8. doi: 10.1016/j.nmd.2008.09.017. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084401

9

Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls.

Rodolico C, Parisi D, Portaro S, Biasini F, Sinicropi S, Ciranni A, Toscano A, Messina S, Musumeci O, Vita G, Girlanda P. Rodolico C, et al. Among authors: toscano a. J Neuromuscul Dis. 2016 Aug 30;3(3):413-418. doi: 10.3233/JND-160148. J Neuromuscul Dis. 2016. PMID: 27854225

10

Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area.

Mazzeo A, Russo M, Di Bella G, Minutoli F, Stancanelli C, Gentile L, Baldari S, Carerj S, Toscano A, Vita G. Mazzeo A, et al. Among authors: toscano a. J Neuromuscul Dis. 2015 Jul 22;2(s2):S39-S48. doi: 10.3233/JND-150091. J Neuromuscul Dis. 2015. PMID: 27858761 Free PMC article.

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