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For: Ravenscroft G, Bryson-Richardson RJ, Nowak KJ, Laing NG. Recent advances in understanding congenital myopathies. F1000Res 2018;7:F1000 Faculty Rev-1921. [PMID: 30631434 DOI: 10.12688/f1000research.16422.1] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
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2 Latham SL, Weiß N, Schwanke K, Thiel C, Croucher DR, Zweigerdt R, Manstein DJ, Taft MH. Myosin-18B Regulates Higher-Order Organization of the Cardiac Sarcomere through Thin Filament Cross-Linking and Thick Filament Dynamics. Cell Rep 2020;32:108090. [PMID: 32877672 DOI: 10.1016/j.celrep.2020.108090] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Choi JH, Huang M, Hyun C, Oh MR, Lee KJ, Cho CH, Lee EH. A muscular hypotonia-associated STIM1 mutant at R429 induces abnormalities in intracellular Ca2+ movement and extracellular Ca2+ entry in skeletal muscle. Sci Rep 2019;9:19140. [PMID: 31844136 DOI: 10.1038/s41598-019-55745-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
4 Conte E, Fonzino A, Cibelli A, De Benedictis V, Imbrici P, Nicchia GP, Pierno S, Camerino GM. Changes in Expression and Cellular Localization of Rat Skeletal Muscle ClC-1 Chloride Channel in Relation to Age, Myofiber Phenotype and PKC Modulation. Front Pharmacol 2020;11:714. [PMID: 32499703 DOI: 10.3389/fphar.2020.00714] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Magee L, Bram JT, Anari JB, Ramo B, Mayer OH, Matsumoto H, Brooks JT, Andras L, Lark R, Fitzgerald R, Truong W, Li Y, Karlin L, Schwend R, Weinstein S, Roye D, Snyder B, Flynn JM, Oetgen M, Smith J, Cahill PJ; PSSG. Outcomes and Complications in Management of Congenital Myopathy Early-Onset Scoliosis. J Pediatr Orthop 2021;41:531-6. [PMID: 34325442 DOI: 10.1097/BPO.0000000000001922] [Reference Citation Analysis]
6 Mubaraki AA. Nemaline Myopathy: A Case Report. Case Rep Neurol 2021;13:499-503. [PMID: 34413753 DOI: 10.1159/000517898] [Reference Citation Analysis]
7 Natera-de Benito D, Ortez C, Jou C, Jimenez-Mallebrera C, Codina A, Carrera-García L, Expósito-Escudero J, Cesar S, Martorell L, Gallano P, Gonzalez-Quereda L, Cuadras D, Colomer J, Yubero D, Palau F, Nascimento A. The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort. Pediatr Neurol 2021;115:50-65. [PMID: 33333461 DOI: 10.1016/j.pediatrneurol.2020.11.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
8 Meunier J, Villar-Quiles RN, Duband-Goulet I, Ferreiro A. Inherited Defects of the ASC-1 Complex in Congenital Neuromuscular Diseases. Int J Mol Sci 2021;22:6039. [PMID: 34204919 DOI: 10.3390/ijms22116039] [Reference Citation Analysis]
9 Werlauff U, Hansen PD, Witting N, Vissing J. Progression or Not - A Small Natural History Study of Genetical Confirmed Congenital Myopathies. J Neuromuscul Dis 2021;8:647-55. [PMID: 33646172 DOI: 10.3233/JND-200574] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Beecroft SJ, Yau KS, Allcock RJN, Mina K, Gooding R, Faiz F, Atkinson VJ, Wise C, Sivadorai P, Trajanoski D, Kresoje N, Ong R, Duff RM, Cabrera-Serrano M, Nowak KJ, Pachter N, Ravenscroft G, Lamont PJ, Davis MR, Laing NG. Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience. Ann Clin Transl Neurol 2020;7:353-62. [PMID: 32153140 DOI: 10.1002/acn3.51002] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]