Tasca G - Search Results

1

Radiomics and machine learning applied to STIR sequence for prediction of quantitative parameters in facioscapulohumeral disease.

Colelli G, Barzaghi L, Paoletti M, Monforte M, Bergsland N, Manco G, Deligianni X, Santini F, Ricci E, Tasca G, Mira A, Figini S, Pichiecchio A. Colelli G, et al. Among authors: tasca g. Front Neurol. 2023 Feb 24;14:1105276. doi: 10.3389/fneur.2023.1105276. eCollection 2023. Front Neurol. 2023. PMID: 36908599 Free PMC article.

2

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

3

A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia.

Luigetti M, Modoni A, Renna R, Silvestri G, Ricci E, Montano N, Tasca G, Papacci M, Monforte M, Conte A, Pomponi MG, Sabatelli M. Luigetti M, et al. Among authors: tasca g. Clin Neurol Neurosurg. 2010 Nov;112(9):794-7. doi: 10.1016/j.clineuro.2010.05.001. Epub 2010 May 26. Clin Neurol Neurosurg. 2010. PMID: 20537790

4

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

5

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

6

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

7

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

8

An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patients.

Pavoni E, Sciandra F, Tasca G, Tittarelli R, Bozzi M, Giardina B, Ricci E, Brancaccio A. Pavoni E, et al. Among authors: tasca g. Open Neurol J. 2011;5:68-74. doi: 10.2174/1874205X01105010068. Epub 2011 Oct 20. Open Neurol J. 2011. PMID: 22046204 Free PMC article.

9

Muscle imaging findings in GNE myopathy.

Tasca G, Ricci E, Monforte M, Laschena F, Ottaviani P, Rodolico C, Barca E, Silvestri G, Iannaccone E, Mirabella M, Broccolini A. Tasca G, et al. J Neurol. 2012 Jul;259(7):1358-65. doi: 10.1007/s00415-011-6357-6. Epub 2012 Jan 10. J Neurol. 2012. PMID: 22231866

10

New phenotype and pathology features in MYH7-related distal myopathy.

Tasca G, Ricci E, Penttilä S, Monforte M, Giglio V, Ottaviani P, Camastra G, Silvestri G, Udd B. Tasca G, et al. Neuromuscul Disord. 2012 Jul;22(7):640-7. doi: 10.1016/j.nmd.2012.03.003. Epub 2012 Apr 20. Neuromuscul Disord. 2012. PMID: 22521714

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