Lamperti C - Search Results

1

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.

2

Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature.

Remiche G, Ronchi D, Magri F, Lamperti C, Bordoni A, Moggio M, Bresolin N, Comi GP. Remiche G, et al. Among authors: lamperti c. J Neurol. 2014 Jan;261(1):83-97. doi: 10.1007/s00415-013-7137-2. Epub 2013 Oct 25. J Neurol. 2014. PMID: 24158270 Review.

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

Multi-system neurological disease is common in patients with OPA1 mutations.

Yu-Wai-Man P, Griffiths PG, Gorman GS, Lourenco CM, Wright AF, Auer-Grumbach M, Toscano A, Musumeci O, Valentino ML, Caporali L, Lamperti C, Tallaksen CM, Duffey P, Miller J, Whittaker RG, Baker MR, Jackson MJ, Clarke MP, Dhillon B, Czermin B, Stewart JD, Hudson G, Reynier P, Bonneau D, Marques W Jr, Lenaers G, McFarland R, Taylor RW, Turnbull DM, Votruba M, Zeviani M, Carelli V, Bindoff LA, Horvath R, Amati-Bonneau P, Chinnery PF. Yu-Wai-Man P, et al. Among authors: lamperti c. Brain. 2010 Mar;133(Pt 3):771-86. doi: 10.1093/brain/awq007. Epub 2010 Feb 15. Brain. 2010. PMID: 20157015 Free PMC article.

5

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation.

Bersano A, Del Bo R, Lamperti C, Ghezzi S, Fagiolari G, Fortunato F, Ballabio E, Moggio M, Candelise L, Galimberti D, Virgilio R, Lanfranconi S, Torrente Y, Carpo M, Bresolin N, Comi GP, Corti S. Bersano A, et al. Among authors: lamperti c. Neurobiol Aging. 2009 May;30(5):752-8. doi: 10.1016/j.neurobiolaging.2007.08.009. Epub 2007 Sep 24. Neurobiol Aging. 2009. PMID: 17889967

6

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.

Magri F, Govoni A, D'Angelo MG, Del Bo R, Ghezzi S, Sandra G, Turconi AC, Sciacco M, Ciscato P, Bordoni A, Tedeschi S, Fortunato F, Lucchini V, Bonato S, Lamperti C, Coviello D, Torrente Y, Corti S, Moggio M, Bresolin N, Comi GP. Magri F, et al. Among authors: lamperti c. J Neurol. 2011 Sep;258(9):1610-23. doi: 10.1007/s00415-011-5979-z. Epub 2011 Mar 12. J Neurol. 2011. PMID: 21399986

7

Effects of interleukin-8 on suppression of human lymphocyte polarization and migration by anti-LFA-1 antibody.

Torre D, Ferrario G, Lamperti C, Issi M, Tambini R, Speranza F. Torre D, et al. Among authors: lamperti c. Eur Cytokine Netw. 1992 Nov-Dec;3(6):565-70. Eur Cytokine Netw. 1992. PMID: 1363595

8

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

9

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

10

Women with pregnancy-related polymyositis and high serum CK levels in the newborn.

Messina S, Fagiolari G, Lamperti C, Cavaletti G, Prelle A, Scarlato G, Bresolin M, Moggio M, Sciacco M. Messina S, et al. Among authors: lamperti c. Neurology. 2002 Feb 12;58(3):482-4. doi: 10.1212/wnl.58.3.482. Neurology. 2002. PMID: 11839858

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