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27. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Gurgel-Giannetti J, Reed UC, Marie SK, Zanoteli E, Fireman MA, Oliveira AS, Werneck LC, Beggs AH, Zatz M, Vainzof M. J Child Neurol; 2003 Mar; 18(3):235-40. PubMed ID: 12731651 [Abstract] [Full Text] [Related]
31. Congenital Nemaline Myopathy: The Value of Magnetic Resonance Imaging of Muscle. Ennis J, Dyment DA, Michaud J, McMillan HJ. Can J Neurol Sci; 2015 Sep; 42(5):338-40. PubMed ID: 26348902 [No Abstract] [Full Text] [Related]
32. Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathy. Blondelle J, Tallapaka K, Seto JT, Ghassemian M, Clark M, Laitila JM, Bournazos A, Singer JD, Lange S. JCI Insight; 2019 Apr 16; 5(10):. PubMed ID: 30990797 [Abstract] [Full Text] [Related]
33. Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci. Jeannet PY, Mittaz L, Dunand M, Lobrinus JA, Bonafe L, Kuntzer T. Neuromuscul Disord; 2007 Jan 16; 17(1):6-12. PubMed ID: 17157023 [Abstract] [Full Text] [Related]
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38. Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases. Schnitzler LJ, Schreckenbach T, Nadaj-Pakleza A, Stenzel W, Rushing EJ, Van Damme P, Ferbert A, Petri S, Hartmann C, Bornemann A, Meisel A, Petersen JA, Tousseyn T, Thal DR, Reimann J, De Jonghe P, Martin JJ, Van den Bergh PY, Schulz JB, Weis J, Claeys KG. Orphanet J Rare Dis; 2017 May 11; 12(1):86. PubMed ID: 28490364 [Abstract] [Full Text] [Related]