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For: Bertini E, D'Amico A, Gualandi F, Petrini S. Congenital muscular dystrophies: a brief review. Semin Pediatr Neurol 2011;18:277-88. [PMID: 22172424 DOI: 10.1016/j.spen.2011.10.010] [Cited by in Crossref: 63] [Cited by in F6Publishing: 50] [Article Influence: 6.3] [Reference Citation Analysis]
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17 Olchowy C, Olchowy A, Pawluś A, Więckiewicz M, Sconfienza LM. Stiffness of the Masseter Muscle in Children-Establishing the Reference Values in the Pediatric Population Using Shear-Wave Elastography. Int J Environ Res Public Health 2021;18:9619. [PMID: 34574544 DOI: 10.3390/ijerph18189619] [Reference Citation Analysis]
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20 Wood AJ, Currie PD. Analysing regenerative potential in zebrafish models of congenital muscular dystrophy. Int J Biochem Cell Biol 2014;56:30-7. [PMID: 25449259 DOI: 10.1016/j.biocel.2014.10.021] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
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25 Nunes RH, Pacheco FT, da Rocha AJ. Magnetic resonance imaging of anterior temporal lobe cysts in children: discriminating special imaging features in a particular group of diseases. Neuroradiology 2014;56:569-77. [DOI: 10.1007/s00234-014-1356-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
26 Koul R, Al-Yarubi S, Al-Kindy H, Al-Futaisi A, Al-Thihli K, Chacko PA, Sankhla D. Rigid spinal muscular dystrophy and rigid spine syndrome: report of 7 children. J Child Neurol 2014;29:1436-40. [PMID: 23481446 DOI: 10.1177/0883073813479173] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
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31 Plantié E, Migocka-Patrzałek M, Daczewska M, Jagla K. Model organisms in the fight against muscular dystrophy: lessons from drosophila and Zebrafish. Molecules 2015;20:6237-53. [PMID: 25859781 DOI: 10.3390/molecules20046237] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 4.6] [Reference Citation Analysis]
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48 Davignon L, Chauveau C, Julien C, Dill C, Duband-Goulet I, Cabet E, Buendia B, Lilienbaum A, Rendu J, Minot MC, Guichet A, Allamand V, Vadrot N, Fauré J, Odent S, Lazaro L, Leroy JP, Marcorelles P, Dubourg O, Ferreiro A. The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease. Hum Mol Genet 2016;25:1559-73. [PMID: 27008887 DOI: 10.1093/hmg/ddw033] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 2.7] [Reference Citation Analysis]
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