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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Talbot J, Maves L. Skeletal muscle fiber type: using insights from muscle developmental biology to dissect targets for susceptibility and resistance to muscle disease. Wiley Interdiscip Rev Dev Biol 2016;5:518-34. [PMID: 27199166 DOI: 10.1002/wdev.230] [Cited by in Crossref: 110] [Cited by in F6Publishing: 101] [Article Influence: 18.3] [Reference Citation Analysis]
2 Brand P, Dyck PJ, Liu J, Berini S, Selcen D, Milone M. Distal myopathy with coexisting heterozygous TIA1 and MYH7 Variants. Neuromuscul Disord 2016;26:511-5. [PMID: 27282841 DOI: 10.1016/j.nmd.2016.05.012] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
3 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]
4 Rinné S, Ortiz-Bonnin B, Stallmeyer B, Kiper AK, Fortmüller L, Schindler RFR, Herbort-Brand U, Kabir NS, Dittmann S, Friedrich C, Zumhagen S, Gualandi F, Selvatici R, Rapezzi C, Arbustini E, Ferlini A, Fabritz L, Schulze-Bahr E, Brand T, Decher N. POPDC2 a novel susceptibility gene for conduction disorders. J Mol Cell Cardiol 2020;145:74-83. [PMID: 32535041 DOI: 10.1016/j.yjmcc.2020.06.005] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
5 Lin Y, Huang J, Zhu Z, Zhang Z, Xian J, Yang Z, Qin T, Chen L, Huang J, Huang Y, Wu Q, Hu Z, Lin X, Xu G. Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation. Orphanet J Rare Dis 2021;16:496. [PMID: 34819141 DOI: 10.1186/s13023-021-02112-9] [Reference Citation Analysis]
6 Finsterer J, Stöllberger C. Reasons for missing noncompaction in myopathies and vice versa. Cardiovasc Pathol 2018;35:20-2. [PMID: 29730526 DOI: 10.1016/j.carpath.2018.04.002] [Reference Citation Analysis]
7 Li S, Wen H, Du S. Defective sarcomere organization and reduced larval locomotion and fish survival in slow muscle heavy chain 1 (smyhc1) mutants. FASEB J 2020;34:1378-97. [PMID: 31914689 DOI: 10.1096/fj.201900935RR] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
8 Cassandrini D, Trovato R, Rubegni A, Lenzi S, Fiorillo C, Baldacci J, Minetti C, Astrea G, Bruno C, Santorelli FM; Italian Network on Congenital Myopathies. Congenital myopathies: clinical phenotypes and new diagnostic tools. Ital J Pediatr. 2017;43:101. [PMID: 29141652 DOI: 10.1186/s13052-017-0419-z] [Cited by in Crossref: 37] [Cited by in F6Publishing: 26] [Article Influence: 7.4] [Reference Citation Analysis]
9 Rubino A, Bruno G, Mazio F, de Leva MF, Ruggiero L, Santorelli FM, Varone A. Spinal Nerve Roots Abnormalities on MRI in a Child with SURF1 Mitochondrial Disease. Neuropediatrics 2021. [PMID: 34852375 DOI: 10.1055/s-0041-1739135] [Reference Citation Analysis]