Tasca G - Search Results

1

Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies.

Morosetti R, Mirabella M, Gliubizzi C, Broccolini A, Sancricca C, Pescatori M, Gidaro T, Tasca G, Frusciante R, Tonali PA, Cossu G, Ricci E. Morosetti R, et al. Among authors: tasca g. Stem Cells. 2007 Dec;25(12):3173-82. doi: 10.1634/stemcells.2007-0465. Epub 2007 Aug 30. Stem Cells. 2007. PMID: 17761758

2

Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression.

Pescatori M, Broccolini A, Minetti C, Bertini E, Bruno C, D'amico A, Bernardini C, Mirabella M, Silvestri G, Giglio V, Modoni A, Pedemonte M, Tasca G, Galluzzi G, Mercuri E, Tonali PA, Ricci E. Pescatori M, et al. Among authors: tasca g. FASEB J. 2007 Apr;21(4):1210-26. doi: 10.1096/fj.06-7285com. Epub 2007 Jan 30. FASEB J. 2007. PMID: 17264171

3

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: tasca g. Muscle Nerve. 2008 Jan;37(1):111-4. doi: 10.1002/mus.20890. Muscle Nerve. 2008. PMID: 17763460

4

ANCA-related vasculitic neuropathy mimicking motor neuron disease.

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

5

Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemia.

Tasca G, Iorio R, Basile U, Lauriola L, Tartaglione R, Mirabella M, Ricci E, Sabatelli M. Tasca G, et al. J Neurol Sci. 2009 Sep 15;284(1-2):203-4. doi: 10.1016/j.jns.2009.04.035. Epub 2009 May 9. J Neurol Sci. 2009. PMID: 19428026

6

Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy.

Broccolini A, Gidaro T, Tasca G, Morosetti R, Rodolico C, Ricci E, Mirabella M. Broccolini A, et al. Among authors: tasca g. Neurology. 2010 Jul 20;75(3):265-72. doi: 10.1212/WNL.0b013e3181e8e8f1. Neurology. 2010. PMID: 20644153

7

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. 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

8

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: tasca g. 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

9

Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration.

Tasca G, Mirabella M, Berrettini A, Monforte M, Tonali PA, Ricci E. Tasca G, et al. Neurol Sci. 2011 Feb;32(1):171-4. doi: 10.1007/s10072-010-0423-1. Epub 2010 Oct 2. Neurol Sci. 2011. PMID: 20890626

10

CD8(+) T cells in facioscapulohumeral muscular dystrophy patients with inflammatory features at muscle MRI.

Frisullo G, Frusciante R, Nociti V, Tasca G, Renna R, Iorio R, Patanella AK, Iannaccone E, Marti A, Rossi M, Bianco A, Monforte M, Tonali PA, Mirabella M, Batocchi AP, Ricci E. Frisullo G, et al. Among authors: tasca g. J Clin Immunol. 2011 Apr;31(2):155-66. doi: 10.1007/s10875-010-9474-6. Epub 2010 Nov 10. J Clin Immunol. 2011. PMID: 21063901

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