Tonali P - Search Results

1

Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophy.

Mirabella M, Servidei S, Manfredi G, Ricci E, Frustaci A, Bertini E, Rana M, Tonali P. Mirabella M, et al. Among authors: tonali p. Neurology. 1993 Nov;43(11):2342-5. doi: 10.1212/wnl.43.11.2342. Neurology. 1993. PMID: 8232953

2

Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy.

Mirabella M, Galluzzi G, Manfredi G, Bertini E, Ricci E, De Leo R, Tonali P, Servidei S. Mirabella M, et al. Among authors: tonali p. Neurology. 1998 Aug;51(2):592-5. doi: 10.1212/wnl.51.2.592. Neurology. 1998. PMID: 9710043

3

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.

Ricci E, Galluzzi G, Deidda G, Cacurri S, Colantoni L, Merico B, Piazzo N, Servidei S, Vigneti E, Pasceri V, Silvestri G, Mirabella M, Mangiola F, Tonali P, Felicetti L. Ricci E, et al. Among authors: tonali p. Ann Neurol. 1999 Jun;45(6):751-7. doi: 10.1002/1531-8249(199906)45:6<751::aid-ana9>3.0.co;2-m. Ann Neurol. 1999. PMID: 10360767

4

A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.

Servidei S, Capon F, Spinazzola A, Mirabella M, Semprini S, de Rosa G, Gennarelli M, Sangiuolo F, Ricci E, Mohrenweiser HW, Dallapiccola B, Tonali P, Novelli G. Servidei S, et al. Among authors: tonali p. Neurology. 1999 Sep 11;53(4):830-7. doi: 10.1212/wnl.53.4.830. Neurology. 1999. PMID: 10489050

5

GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophy.

Mirabella M, Silvestri G, de Rosa G, Di Giovanni S, Di Muzio A, Uncini A, Tonali P, Servidei S. Mirabella M, et al. Among authors: tonali p. Neurology. 2000 Feb 8;54(3):608-14. doi: 10.1212/wnl.54.3.608. Neurology. 2000. PMID: 10680791

6

Apoptotic features accompany acute quadriplegic myopathy.

Di Giovanni S, Mirabella M, D'Amico A, Tonali P, Servidei S. Di Giovanni S, et al. Among authors: tonali p. Neurology. 2000 Sep 26;55(6):854-8. doi: 10.1212/wnl.55.6.854. Neurology. 2000. PMID: 10994008

7

Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency.

Di Giovanni S, Mirabella M, Spinazzola A, Crociani P, Silvestri G, Broccolini A, Tonali P, Di Mauro S, Servidei S. Di Giovanni S, et al. Among authors: tonali p. Neurology. 2001 Aug 14;57(3):515-8. doi: 10.1212/wnl.57.3.515. Neurology. 2001. PMID: 11502923

8

Heart rate variability in facioscapulohumeral muscular dystrophy.

Della Marca G, Frusciante R, Scatena M, Dittoni S, Testani E, Vollono C, Losurdo A, Scarano E, Colicchio S, Farina B, Gnoni V, Mazza S, Tonali PA, Ricci E. Della Marca G, et al. Among authors: tonali pa. Funct Neurol. 2010 Oct-Dec;25(4):211-6. Funct Neurol. 2010. PMID: 21388582

9

Ultrasound tissue characterization detects preclinical myocardial structural changes in children affected by Duchenne muscular dystrophy.

Giglio V, Pasceri V, Messano L, Mangiola F, Pasquini L, Dello Russo A, Damiani A, Mirabella M, Galluzzi G, Tonali P, Ricci E. Giglio V, et al. Among authors: tonali p. J Am Coll Cardiol. 2003 Jul 16;42(2):309-16. doi: 10.1016/s0735-1097(03)00581-3. J Am Coll Cardiol. 2003. PMID: 12875769 Free article.

10

Insulin-like growth factor I in inclusion-body myositis and human muscle cultures.

Broccolini A, Ricci E, Pescatori M, Papacci M, Gliubizzi C, D'Amico A, Servidei S, Tonali P, Mirabella M. Broccolini A, et al. Among authors: tonali p. J Neuropathol Exp Neurol. 2004 Jun;63(6):650-9. doi: 10.1093/jnen/63.6.650. J Neuropathol Exp Neurol. 2004. PMID: 15217093

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