Ricci E - 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: ricci e. Front Neurol. 2023 Feb 24;14:1105276. doi: 10.3389/fneur.2023.1105276. eCollection 2023. Front Neurol. 2023. PMID: 36908599 Free PMC article.

2

Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutations.

Mercuri E, Topaloglu H, Brockington M, Berardinelli A, Pichiecchio A, Santorelli F, Rutherford M, Talim B, Ricci E, Voit T, Muntoni F. Mercuri E, et al. Among authors: ricci e. Arch Neurol. 2006 Feb;63(2):251-7. doi: 10.1001/archneur.63.2.251. Arch Neurol. 2006. PMID: 16476814

3

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: ricci e. Stem Cells. 2007 Dec;25(12):3173-82. doi: 10.1634/stemcells.2007-0465. Epub 2007 Aug 30. Stem Cells. 2007. PMID: 17761758

4

Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study.

Mercuri E, Messina S, Bruno C, Mora M, Pegoraro E, Comi GP, D'Amico A, Aiello C, Biancheri R, Berardinelli A, Boffi P, Cassandrini D, Laverda A, Moggio M, Morandi L, Moroni I, Pane M, Pezzani R, Pichiecchio A, Pini A, Minetti C, Mongini T, Mottarelli E, Ricci E, Ruggieri A, Saredi S, Scuderi C, Tessa A, Toscano A, Tortorella G, Trevisan CP, Uggetti C, Vasco G, Santorelli FM, Bertini E. Mercuri E, et al. Among authors: ricci e. Neurology. 2009 May 26;72(21):1802-9. doi: 10.1212/01.wnl.0000346518.68110.60. Epub 2009 Mar 18. Neurology. 2009. PMID: 19299310

5

Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine.

Mercuri E, Clements E, Offiah A, Pichiecchio A, Vasco G, Bianco F, Berardinelli A, Manzur A, Pane M, Messina S, Gualandi F, Ricci E, Rutherford M, Muntoni F. Mercuri E, et al. Among authors: ricci e. Ann Neurol. 2010 Feb;67(2):201-8. doi: 10.1002/ana.21846. Ann Neurol. 2010. PMID: 20225280

6

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: ricci e. 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

7

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: ricci e. Neurology. 2010 Jul 20;75(3):265-72. doi: 10.1212/WNL.0b013e3181e8e8f1. Neurology. 2010. PMID: 20644153

8

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: ricci e. 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

9

Congenital muscular dystrophies with cognitive impairment. A population study.

Messina S, Bruno C, Moroni I, Pegoraro E, D'Amico A, Biancheri R, Berardinelli A, Boffi P, Cassandrini D, Farina L, Minetti C, Moggio M, Mongini T, Mottarelli E, Pane M, Pantaleoni C, Pichiecchio A, Pini A, Ricci E, Saredi S, Sframeli M, Tortorella G, Toscano A, Trevisan CP, Uggetti C, Vasco G, Comi GP, Santorelli FM, Bertini E, Mercuri E. Messina S, et al. Among authors: ricci e. Neurology. 2010 Sep 7;75(10):898-903. doi: 10.1212/WNL.0b013e3181f11dd5. Neurology. 2010. PMID: 20820001

10

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

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