Lamperti C - Search Results

1

DiMauro S, Lamperti C. DiMauro S, et al. Among authors: lamperti c. Muscle Nerve. 2001 Aug;24(8):984-99. doi: 10.1002/mus.1103. Muscle Nerve. 2001. PMID: 11439374 Review.

2

Nanopore long-read next-generation sequencing for detection of mitochondrial DNA large-scale deletions.

Frascarelli C, Zanetti N, Nasca A, Izzo R, Lamperti C, Lamantea E, Legati A, Ghezzi D. Frascarelli C, et al. Among authors: lamperti c. Front Genet. 2023 Jun 29;14:1089956. doi: 10.3389/fgene.2023.1089956. eCollection 2023. Front Genet. 2023. PMID: 37456669 Free PMC article.

3

Clinicopathological features of genetically confirmed Danon disease.

Sugie K, Yamamoto A, Murayama K, Oh SJ, Takahashi M, Mora M, Riggs JE, Colomer J, Iturriaga C, Meloni A, Lamperti C, Saitoh S, Byrne E, DiMauro S, Nonaka I, Hirano M, Nishino I. Sugie K, et al. Among authors: lamperti c. Neurology. 2002 Jun 25;58(12):1773-8. doi: 10.1212/wnl.58.12.1773. Neurology. 2002. PMID: 12084876 Review.

4

Cerebellar ataxia and coenzyme Q10 deficiency.

Lamperti C, Naini A, Hirano M, De Vivo DC, Bertini E, Servidei S, Valeriani M, Lynch D, Banwell B, Berg M, Dubrovsky T, Chiriboga C, Angelini C, Pegoraro E, DiMauro S. Lamperti C, et al. Neurology. 2003 Apr 8;60(7):1206-8. doi: 10.1212/01.wnl.0000055089.39373.fc. Neurology. 2003. PMID: 12682339

5

Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes.

Mancuso M, Filosto M, Tsujino S, Lamperti C, Shanske S, Coquet M, Desnuelle C, DiMauro S. Mancuso M, et al. Among authors: lamperti c. Arch Neurol. 2003 Oct;60(10):1445-7. doi: 10.1001/archneur.60.10.1445. Arch Neurol. 2003. PMID: 14568816

6

Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency.

Gironi M, Lamperti C, Nemni R, Moggio M, Comi G, Guerini FR, Ferrante P, Canal N, Naini A, Bresolin N, DiMauro S. Gironi M, et al. Among authors: lamperti c. Neurology. 2004 Mar 9;62(5):818-20. doi: 10.1212/01.wnl.0000113719.67643.b7. Neurology. 2004. PMID: 15007142

7

Muscle coenzyme Q10 level in statin-related myopathy.

Lamperti C, Naini AB, Lucchini V, Prelle A, Bresolin N, Moggio M, Sciacco M, Kaufmann P, DiMauro S. Lamperti C, et al. Arch Neurol. 2005 Nov;62(11):1709-12. doi: 10.1001/archneur.62.11.1709. Arch Neurol. 2005. PMID: 16286544 Clinical Trial.

8

Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.

Crugnola V, Lamperti C, Lucchini V, Ronchi D, Peverelli L, Prelle A, Sciacco M, Bordoni A, Fassone E, Fortunato F, Corti S, Silani V, Bresolin N, Di Mauro S, Comi GP, Moggio M. Crugnola V, et al. Among authors: lamperti c. Arch Neurol. 2010 Jul;67(7):849-54. doi: 10.1001/archneurol.2010.128. Arch Neurol. 2010. PMID: 20625092

9

Ultrastructural mitochondrial abnormalities in patients with sporadic amyotrophic lateral sclerosis.

Napoli L, Crugnola V, Lamperti C, Silani V, Di Mauro S, Bresolin N, Moggio M. Napoli L, et al. Among authors: lamperti c. Arch Neurol. 2011 Dec;68(12):1612-3. doi: 10.1001/archneur.68.12.1612. Arch Neurol. 2011. PMID: 22159065 No abstract available.

10

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score.

Lamperti C, Fabbri G, Vercelli L, D'Amico R, Frusciante R, Bonifazi E, Fiorillo C, Borsato C, Cao M, Servida M, Greco F, Di Leo R, Volpi L, Manzoli C, Cudia P, Pastorello E, Ricciardi L, Siciliano G, Galluzzi G, Rodolico C, Santoro L, Tomelleri G, Angelini C, Ricci E, Palmucci L, Moggio M, Tupler R. Lamperti C, et al. Muscle Nerve. 2010 Aug;42(2):213-7. doi: 10.1002/mus.21671. Muscle Nerve. 2010. PMID: 20544930

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