Monforte M - Search Results

1

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. Among authors: monforte m. J Neurol. 2012 Jul;259(7):1358-65. doi: 10.1007/s00415-011-6357-6. Epub 2012 Jan 10. J Neurol. 2012. PMID: 22231866

2

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: monforte m. 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

3

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: monforte 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

4

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. Among authors: monforte m. Neurol Sci. 2011 Feb;32(1):171-4. doi: 10.1007/s10072-010-0423-1. Epub 2010 Oct 2. Neurol Sci. 2011. PMID: 20890626

5

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: monforte m. 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

6

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. Among authors: monforte m. 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

7

Muscle MRI in female carriers of dystrophinopathy.

Tasca G, Monforte M, Iannaccone E, Laschena F, Ottaviani P, Silvestri G, Masciullo M, Mirabella M, Servidei S, Ricci E. Tasca G, et al. Among authors: monforte m. Eur J Neurol. 2012 Sep;19(9):1256-60. doi: 10.1111/j.1468-1331.2012.03753.x. Epub 2012 May 15. Eur J Neurol. 2012. PMID: 22583668

8

Different molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles.

Tasca G, Pescatori M, Monforte M, Mirabella M, Iannaccone E, Frusciante R, Cubeddu T, Laschena F, Ottaviani P, Ricci E. Tasca G, et al. Among authors: monforte m. PLoS One. 2012;7(6):e38779. doi: 10.1371/journal.pone.0038779. Epub 2012 Jun 13. PLoS One. 2012. PMID: 22719944 Free PMC article.

9

Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia.

Tasca G, Odgerel Z, Monforte M, Aurino S, Clarke NF, Waddell LB, Udd B, Ricci E, Goldfarb LG. Tasca G, et al. Among authors: monforte m. Muscle Nerve. 2012 Aug;46(2):275-82. doi: 10.1002/mus.23349. Muscle Nerve. 2012. PMID: 22806379 Free PMC article.

10

Muscle MRI in Becker muscular dystrophy.

Tasca G, Iannaccone E, Monforte M, Masciullo M, Bianco F, Laschena F, Ottaviani P, Pelliccioni M, Pane M, Mercuri E, Ricci E. Tasca G, et al. Among authors: monforte m. Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S100-6. doi: 10.1016/j.nmd.2012.05.015. Neuromuscul Disord. 2012. PMID: 22980760

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