Sabatelli M - Search Results

1

Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking.

Swan AH, Schindler RFR, Savarese M, Mayer I, Rinné S, Bleser F, Schänzer A, Hahn A, Sabatelli M, Perna F, Chapman K, Pfuhl M, Spivey AC, Decher N, Udd B, Tasca G, Brand T. Swan AH, et al. Among authors: sabatelli m. Acta Neuropathol Commun. 2023 Jan 9;11(1):4. doi: 10.1186/s40478-022-01501-w. Acta Neuropathol Commun. 2023. PMID: 36624536 Free PMC article.

2

An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene.

Gidaro T, Modoni A, Sabatelli M, Tasca G, Broccolini A, Mirabella M. Gidaro T, et al. Among authors: sabatelli m. Muscle Nerve. 2008 Jan;37(1):111-4. doi: 10.1002/mus.20890. Muscle Nerve. 2008. PMID: 17763460

3

ANCA-related vasculitic neuropathy mimicking motor neuron disease.

Luigetti M, Tasca G, Mirabella M, Tonali PA, Sabatelli M. Luigetti M, et al. Among authors: sabatelli m. Acta Neurol Belg. 2008 Sep;108(3):109-11. Acta Neurol Belg. 2008. PMID: 19115676

4

An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation.

Tasca G, Mirabella M, Broccolini A, Monforte M, Sabatelli M, Biscione GL, Piluso G, Gualandi F, Tonali PA, Udd B, Ricci E. Tasca G, et al. Among authors: sabatelli m. Neuromuscul Disord. 2010 Nov;20(11):730-4. doi: 10.1016/j.nmd.2010.07.269. Epub 2010 Aug 13. Neuromuscul Disord. 2010. PMID: 20708934

5

A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype.

Luigetti M, Fabrizi GM, Madia F, Ferrarini M, Conte A, Del Grande A, Tasca G, Tonali PA, Sabatelli M. Luigetti M, et al. Among authors: sabatelli m. J Neurol Sci. 2010 Nov 15;298(1-2):114-7. doi: 10.1016/j.jns.2010.09.008. Epub 2010 Sep 25. J Neurol Sci. 2010. PMID: 20870250

6

Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patients.

Bernardini C, Censi F, Lattanzi W, Barba M, Calcagnini G, Giuliani A, Tasca G, Sabatelli M, Ricci E, Michetti F. Bernardini C, et al. Among authors: sabatelli m. PLoS One. 2013;8(2):e57739. doi: 10.1371/journal.pone.0057739. Epub 2013 Feb 28. PLoS One. 2013. PMID: 23469062 Free PMC article.

7

Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods.

Tasca G, Fattori F, Monforte M, Hedberg-Oldfors C, Sabatelli M, Udd B, Boldrini R, Bertini E, Ricci E, Oldfors A. Tasca G, et al. Among authors: sabatelli m. J Neurol. 2016 Oct;263(10):2133-5. doi: 10.1007/s00415-016-8268-z. Epub 2016 Aug 20. J Neurol. 2016. PMID: 27544502 No abstract available.

8

Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients.

Di Pietro L, Baranzini M, Berardinelli MG, Lattanzi W, Monforte M, Tasca G, Conte A, Logroscino G, Michetti F, Ricci E, Sabatelli M, Bernardini C. Di Pietro L, et al. Among authors: sabatelli m. Sci Rep. 2017 Aug 25;7(1):9538. doi: 10.1038/s41598-017-10161-z. Sci Rep. 2017. PMID: 28842714 Free PMC article.

9

SOD1 p.D12Y variant is associated with amyotrophic lateral sclerosis/distal myopathy spectrum.

Tasca G, Lattante S, Marangi G, Conte A, Bernardo D, Bisogni G, Mandich P, Zollino M, Ragozzino E, Udd B, Sabatelli M. Tasca G, et al. Among authors: sabatelli m. Eur J Neurol. 2020 Jul;27(7):1304-1309. doi: 10.1111/ene.14246. Epub 2020 Apr 28. Eur J Neurol. 2020. PMID: 32250500

10

Response to: SOD1 mutations in adult-onset distal spinal muscular atrophy.

Tasca G, Udd B, Sabatelli M. Tasca G, et al. Among authors: sabatelli m. Eur J Neurol. 2020 Nov;27(11):e74. doi: 10.1111/ene.14425. Epub 2020 Jul 28. Eur J Neurol. 2020. PMID: 32618054 No abstract available.

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