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For: Clarke NF. Congenital fibre type disproportion--a syndrome at the crossroads of the congenital myopathies. Neuromuscul Disord. 2011;21:252-253. [PMID: 21420627 DOI: 10.1016/j.nmd.2011.02.015] [Cited by in Crossref: 18] [Cited by in F6Publishing: 13] [Article Influence: 1.6] [Reference Citation Analysis]
Number Citing Articles
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5 Clarke NF, Waddell LB, Sie LT, van Bon BW, Mclean C, Clark D, Kornberg A, Lammens M, North KN. Mutations in TPM2 and congenital fibre type disproportion. Neuromuscular Disorders 2012;22:955-8. [DOI: 10.1016/j.nmd.2012.06.002] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 1.6] [Reference Citation Analysis]
6 Sewry CA, Wallgren-Pettersson C. Myopathology in congenital myopathies. Neuropathol Appl Neurobiol 2017;43:5-23. [PMID: 27976420 DOI: 10.1111/nan.12369] [Cited by in Crossref: 44] [Cited by in F6Publishing: 31] [Article Influence: 11.0] [Reference Citation Analysis]
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9 Borovikov YS, Karpicheva OE, Simonyan AO, Avrova SV, Rogozovets EA, Sirenko VV, Redwood CS. The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies. Int J Mol Sci 2018;19:E3975. [PMID: 30544720 DOI: 10.3390/ijms19123975] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
10 Rodenas S, Guo LT, Shelton GD. Myopathy associated with congenital fibre type disproportion in a young dog. J Comp Pathol 2012;147:486-90. [PMID: 22789857 DOI: 10.1016/j.jcpa.2012.05.003] [Reference Citation Analysis]
11 Iannaccone ST, Castro D. Congenital muscular dystrophies and congenital myopathies. Continuum (Minneap Minn) 2013;19:1509-34. [PMID: 24305446 DOI: 10.1212/01.CON.0000440658.03557.f1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
12 Yang HM, Guo JX, Yang YM. Congenital fiber-type disproportion presenting with type II respiratory failure after delivery: A case report. World J Clin Cases 2021; 9(7): 1748-1754 [PMID: 33728321 DOI: 10.12998/wjcc.v9.i7.1748] [Reference Citation Analysis]
13 Kondo E, Nishimura T, Kosho T, Inaba Y, Mitsuhashi S, Ishida T, Baba A, Koike K, Nishino I, Nonaka I, Furukawa T, Saito K. Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing. Am J Med Genet 2012;158A:772-8. [DOI: 10.1002/ajmg.a.35243] [Cited by in Crossref: 23] [Cited by in F6Publishing: 21] [Article Influence: 2.3] [Reference Citation Analysis]
14 Ogasawara M, Nishino I. A review of core myopathy: central core disease, multiminicore disease, dusty core disease, and core-rod myopathy. Neuromuscul Disord 2021;31:968-77. [PMID: 34627702 DOI: 10.1016/j.nmd.2021.08.015] [Reference Citation Analysis]
15 Ruggiero L, Fiorillo C, Gibertini S, De Stefano F, Manganelli F, Iodice R, Vitale F, Zanotti S, Galderisi M, Mora M, Santoro L. A rare mutation in MYH7 gene occurs with overlapping phenotype. Biochem Biophys Res Commun 2015;457:262-6. [PMID: 25576864 DOI: 10.1016/j.bbrc.2014.12.098] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]