Fagiolari G - Search Results

1

Lack of apoptosis in patients with progressive external ophthalmoplegia and mutated adenine nucleotide translocator-1 gene.

Fagiolari G, Sciacco M, Chiveri L, Lamperti C, Comi GP, Scarlato G, Moggio M, Prelle A. Fagiolari G, et al. Muscle Nerve. 2002 Aug;26(2):265-9. doi: 10.1002/mus.10172. Muscle Nerve. 2002. PMID: 12210391

2

Lack of anionic phospholipid calcium binding sites in Duchenne muscular dystrophy.

Moggio M, Fagiolari G, Prelle A, Gallanti A, Sciacco M, Scarlato G. Moggio M, et al. Among authors: fagiolari g. Muscle Nerve. 1992 Mar;15(3):325-31. doi: 10.1002/mus.880150311. Muscle Nerve. 1992. PMID: 1557080

3

Lack of apoptosis in mitochondrial encephalomyopathies.

Sciacco M, Fagiolari G, Lamperti C, Messina S, Bazzi P, Napoli L, Chiveri L, Prelle A, Comi GP, Bresolin N, Scarlato G, Moggio M. Sciacco M, et al. Among authors: fagiolari g. Neurology. 2001 Apr 24;56(8):1070-4. doi: 10.1212/wnl.56.8.1070. Neurology. 2001. PMID: 11320180

4

A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy.

Sciacco M, Prelle A, Fagiolari G, Bordoni A, Crimi M, Di Fonzo A, Ciscato P, Lamperti C, D'Adda E, Jann S, Bresolin N, Comi GP, Moggio M. Sciacco M, et al. Among authors: fagiolari g. J Neurol Sci. 2005 Dec 15;239(1):21-4. doi: 10.1016/j.jns.2005.07.008. Epub 2005 Sep 15. J Neurol Sci. 2005. PMID: 16168441

5

Sporadic late-onset nemaline myopathy in a woman with multiple myeloma successfully treated with lenalidomide/dexamethasone.

Montagnese F, Portaro S, Musumeci O, Migliorato A, Moggio M, Fagiolari G, Rodolico C. Montagnese F, et al. Among authors: fagiolari g. Muscle Nerve. 2015 Jun;51(6):934-5. doi: 10.1002/mus.24545. Epub 2015 Jan 5. Muscle Nerve. 2015. PMID: 25524603 No abstract available.

6

RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy.

Reyes A, Melchionda L, Nasca A, Carrara F, Lamantea E, Zanolini A, Lamperti C, Fang M, Zhang J, Ronchi D, Bonato S, Fagiolari G, Moggio M, Ghezzi D, Zeviani M. Reyes A, et al. Among authors: fagiolari g. Am J Hum Genet. 2015 Jul 2;97(1):186-93. doi: 10.1016/j.ajhg.2015.05.013. Epub 2015 Jun 18. Am J Hum Genet. 2015. PMID: 26094573 Free PMC article.

7

Ultrastructural localization of calcium binding sites on human muscle cell surface.

Moggio M, Jann S, Adobbati L, Prelle A, Gallanti A, Fagiolari G, Pellegrini G, Scarlato G. Moggio M, et al. Among authors: fagiolari g. Muscle Nerve. 1989 Nov;12(11):910-4. doi: 10.1002/mus.880121107. Muscle Nerve. 1989. PMID: 2558316

8

Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy.

Moggio M, Prelle A, Fagiolari G, Checcarelli N, Sciacco M, Ciscato P, Scarlato G. Moggio M, et al. Among authors: fagiolari g. Muscle Nerve. 1994 May;17(5):485-8. doi: 10.1002/mus.880170503. Muscle Nerve. 1994. PMID: 8159177

9

Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle.

Prelle A, Rigoletto C, Moggio M, Sciacco M, Comi GP, Ciscato P, Fagiolari G, Rapuzzi S, Bignotti V, Scarlato G. Prelle A, et al. Among authors: fagiolari g. J Neurol Sci. 1996 Sep 1;140(1-2):132-6. doi: 10.1016/0022-510x(96)00129-3. J Neurol Sci. 1996. PMID: 8866439

10

Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.

Sciacco M, Prelle A, Comi GP, Napoli L, Battistel A, Bresolin N, Tancredi L, Lamperti C, Bordoni A, Fagiolari G, Ciscato P, Chiveri L, Perini MP, Fortunato F, Adobbati L, Messina S, Toscano A, Martinelli-Boneschi F, Papadimitriou A, Scarlato G, Moggio M. Sciacco M, et al. Among authors: fagiolari g. J Neurol. 2001 Sep;248(9):778-88. doi: 10.1007/s004150170094. J Neurol. 2001. PMID: 11596783

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