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For: Quijano-roy S, Carlier RY, Fischer D. Muscle Imaging in Congenital Myopathies. Seminars in Pediatric Neurology 2011;18:221-9. [DOI: 10.1016/j.spen.2011.10.003] [Cited by in Crossref: 49] [Cited by in F6Publishing: 40] [Article Influence: 4.5] [Reference Citation Analysis]
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12 Fiorillo C, Astrea G, Savarese M, Cassandrini D, Brisca G, Trucco F, Pedemonte M, Trovato R, Ruggiero L, Vercelli L, D'Amico A, Tasca G, Pane M, Fanin M, Bello L, Broda P, Musumeci O, Rodolico C, Messina S, Vita GL, Sframeli M, Gibertini S, Morandi L, Mora M, Maggi L, Petrucci A, Massa R, Grandis M, Toscano A, Pegoraro E, Mercuri E, Bertini E, Mongini T, Santoro L, Nigro V, Minetti C, Santorelli FM, Bruno C; Italian Network on Congenital Myopathies. MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients. Orphanet J Rare Dis 2016;11:91. [PMID: 27387980 DOI: 10.1186/s13023-016-0476-1] [Cited by in Crossref: 38] [Cited by in F6Publishing: 35] [Article Influence: 6.3] [Reference Citation Analysis]
13 Hafner P, Bonati U, Fischmann A, Schneider J, Frank S, Morris-Rosendahl DJ, Dumea A, Heinimann K, Fischer D. Skeletal muscle MRI of the lower limbs in congenital muscular dystrophy patients with novel POMT1 and POMT2 mutations. Neuromuscul Disord 2014;24:321-4. [PMID: 24556424 DOI: 10.1016/j.nmd.2014.01.009] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 1.9] [Reference Citation Analysis]
14 Gineste C, De Winter JM, Kohl C, Witt CC, Giannesini B, Brohm K, Le Fur Y, Gretz N, Vilmen C, Pecchi E, Jubeau M, Cozzone PJ, Stienen GJ, Granzier H, Labeit S, Ottenheijm CA, Bendahan D, Gondin J. In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype. Neuromuscul Disord 2013;23:357-69. [PMID: 23375831 DOI: 10.1016/j.nmd.2012.12.011] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 2.0] [Reference Citation Analysis]
15 Mercier S, Magot A, Caillon F, Isidor B, David A, Ferrer X, Vital A, Coquet M, Penttilä S, Udd B, Mussini JM, Pereon Y. Muscle magnetic resonance imaging abnormalities in X-linked myopathy with excessive autophagy. Muscle Nerve 2015;52:673-80. [PMID: 25809233 DOI: 10.1002/mus.24664] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
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17 Renard D, Thouvenot E. Lower limb muscle atrophy on MRI as a guide in the diagnosis of muscle diseases. Acta Neurol Belg 2017;117:635-6. [PMID: 28602008 DOI: 10.1007/s13760-017-0804-9] [Reference Citation Analysis]
18 Warman Chardon J, Díaz-manera J, Tasca G, Bönnemann CG, Gómez-andrés D, Heerschap A, Mercuri E, Muntoni F, Pichiecchio A, Ricci E, Walter MC, Hanna M, Jungbluth H, Morrow JM, Fernández-torrón R, Udd B, Vissing J, Yousry T, Quijano-roy S, Straub V, Carlier RY. MYO-MRI diagnostic protocols in genetic myopathies. Neuromuscular Disorders 2019;29:827-41. [DOI: 10.1016/j.nmd.2019.08.011] [Cited by in Crossref: 19] [Cited by in F6Publishing: 13] [Article Influence: 6.3] [Reference Citation Analysis]
19 Alejaldre A, Díaz-manera J, Ravaglia S, Tibaldi EC, D’amore F, Morís G, Muelas N, Vílchez JJ, García-medina A, Usón M, Martínez García FA, Illa I, Pichiecchio A. Trunk muscle involvement in late-onset Pompe disease: Study of thirty patients. Neuromuscular Disorders 2012;22:S148-54. [DOI: 10.1016/j.nmd.2012.05.011] [Cited by in Crossref: 36] [Cited by in F6Publishing: 30] [Article Influence: 3.6] [Reference Citation Analysis]
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22 Wattjes MP, Fischmann A, Fischer D. [Imaging of primary muscular diseases : What do neurologists expect from radiologists?]. Radiologe 2017;57:1005-11. [PMID: 28986620 DOI: 10.1007/s00117-017-0309-9] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
23 Biancalana V, Scheidecker S, Miguet M, Laquerrière A, Romero NB, Stojkovic T, Abath Neto O, Mercier S, Voermans N, Tanner L, Rogers C, Ollagnon-Roman E, Roper H, Boutte C, Ben-Shachar S, Lornage X, Vasli N, Schaefer E, Laforet P, Pouget J, Moerman A, Pasquier L, Marcorelle P, Magot A, Küsters B, Streichenberger N, Tranchant C, Dondaine N, Schneider R, Gasnier C, Calmels N, Kremer V, Nguyen K, Perrier J, Kamsteeg EJ, Carlier P, Carlier RY, Thompson J, Boland A, Deleuze JF, Fardeau M, Zanoteli E, Eymard B, Laporte J. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta Neuropathol 2017;134:889-904. [PMID: 28685322 DOI: 10.1007/s00401-017-1748-0] [Cited by in Crossref: 31] [Cited by in F6Publishing: 30] [Article Influence: 6.2] [Reference Citation Analysis]
24 Catteruccia M, Fattori F, Codemo V, Ruggiero L, Maggi L, Tasca G, Fiorillo C, Pane M, Berardinelli A, Verardo M, Bragato C, Mora M, Morandi L, Bruno C, Santoro L, Pegoraro E, Mercuri E, Bertini E, D'Amico A. Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohort. Neuromuscul Disord 2013;23:229-38. [PMID: 23394783 DOI: 10.1016/j.nmd.2012.12.009] [Cited by in Crossref: 41] [Cited by in F6Publishing: 28] [Article Influence: 4.6] [Reference Citation Analysis]
25 Ardissone A, Bragato C, Blasevich F, Maccagnano E, Salerno F, Gandioli C, Morandi L, Mora M, Moroni I. SEPN1-related myopathy in three patients: novel mutations and diagnostic clues. Eur J Pediatr 2016;175:1113-8. [PMID: 26780752 DOI: 10.1007/s00431-015-2685-3] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 2.2] [Reference Citation Analysis]
26 Tomas X, Milisenda JC, Garcia-Diez AI, Prieto-Gonzalez S, Faruch M, Pomes J, Grau-Junyent JM. Whole-body MRI and pathological findings in adult patients with myopathies. Skeletal Radiol 2019;48:653-76. [PMID: 30377729 DOI: 10.1007/s00256-018-3107-1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
27 Jarraya M, Quijano-Roy S, Monnier N, Béhin A, Avila-Smirnov D, Romero NB, Allamand V, Richard P, Barois A, May A, Estournet B, Mercuri E, Carlier PG, Carlier RY. Whole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutations. Neuromuscul Disord 2012;22 Suppl 2:S137-47. [PMID: 22980765 DOI: 10.1016/j.nmd.2012.06.347] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 3.1] [Reference Citation Analysis]
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31 Straub V, Carlier PG, Mercuri E. TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 February 2011, Rome, Italy. Neuromuscul Disord 2012;22 Suppl 2:S42-53. [PMID: 22980768 DOI: 10.1016/j.nmd.2012.08.002] [Cited by in Crossref: 73] [Cited by in F6Publishing: 56] [Article Influence: 8.1] [Reference Citation Analysis]
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35 Bönnemann CG, Wang CH, Quijano-Roy S, Deconinck N, Bertini E, Ferreiro A, Muntoni F, Sewry C, Béroud C, Mathews KD, Moore SA, Bellini J, Rutkowski A, North KN; Members of International Standard of Care Committee for Congenital Muscular Dystrophies. Diagnostic approach to the congenital muscular dystrophies. Neuromuscul Disord 2014;24:289-311. [PMID: 24581957 DOI: 10.1016/j.nmd.2013.12.011] [Cited by in Crossref: 189] [Cited by in F6Publishing: 158] [Article Influence: 23.6] [Reference Citation Analysis]
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37 Gineste C, Duhamel G, Le Fur Y, Vilmen C, Cozzone PJ, Nowak KJ, Bendahan D, Gondin J. Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism. PLoS One 2013;8:e72294. [PMID: 23977274 DOI: 10.1371/journal.pone.0072294] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 1.3] [Reference Citation Analysis]
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40 Carlier R, Quijano-roy S. Myoimaging in Congenital Myopathies. Seminars in Pediatric Neurology 2019;29:30-43. [DOI: 10.1016/j.spen.2019.03.019] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
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