Tonali P - Search Results

1

Analysis of peristaltic reflex in young mdx dystrophic mice.

Mancinelli R, Tonali P, Servidei S, Azzena GB. Mancinelli R, et al. Among authors: tonali p. Neurosci Lett. 1995 Jun 2;192(1):57-60. doi: 10.1016/0304-3940(95)11609-z. Neurosci Lett. 1995. PMID: 7675311

2

Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy.

Brahe C, Servidei S, Zappata S, Ricci E, Tonali P, Neri G. Brahe C, et al. Among authors: tonali p. Lancet. 1995 Sep 16;346(8977):741-2. doi: 10.1016/s0140-6736(95)91507-9. Lancet. 1995. PMID: 7658877

3

Retroviral vector-mediated gene transfer into human primary myogenic cells leads to expression in muscle fibers in vivo.

Salvatori G, Ferrari G, Mezzogiorno A, Servidei S, Coletta M, Tonali P, Giavazzi R, Cossu G, Mavilio F. Salvatori G, et al. Among authors: tonali p. Hum Gene Ther. 1993 Dec;4(6):713-23. doi: 10.1089/hum.1993.4.6-713. Hum Gene Ther. 1993. PMID: 8186286

4

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

5

Functional involvement of cerebral cortex in Duchenne muscular dystrophy.

Di Lazzaro V, Restuccia D, Servidei S, Nardone R, Oliviero A, Profice P, Mangiola F, Tonali P, Rothwell JC. Di Lazzaro V, et al. Among authors: tonali p. Muscle Nerve. 1998 May;21(5):662-4. doi: 10.1002/(sici)1097-4598(199805)21:5<662::aid-mus18>3.0.co;2-x. Muscle Nerve. 1998. PMID: 9572251

6

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

7

Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis.

Tricarico D, Servidei S, Tonali P, Jurkat-Rott K, Camerino DC. Tricarico D, et al. Among authors: tonali p. J Clin Invest. 1999 Mar;103(5):675-82. doi: 10.1172/JCI4552. J Clin Invest. 1999. PMID: 10074484 Free PMC article.

8

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

9

Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanism.

Mirabella M, Di Giovanni S, Silvestri G, Tonali P, Servidei S. Mirabella M, et al. Among authors: tonali p. Brain. 2000 Jan;123 ( Pt 1):93-104. doi: 10.1093/brain/123.1.93. Brain. 2000. PMID: 10611124

10

Presymptomatic diagnosis of SMA III by genotype analysis.

Brahe C, Zappata S, Velonà I, Bertini E, Servidei S, Tonali P, Neri G. Brahe C, et al. Among authors: tonali p. Am J Med Genet. 1993 Feb 1;45(3):408-11. doi: 10.1002/ajmg.1320450331. Am J Med Genet. 1993. PMID: 8434634

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

565 results

Search Page