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Genetics of cardiac electrical disease.
Perrin MJ, Gollob MH. Perrin MJ, et al. Among authors: gollob mh. Can J Cardiol. 2013 Jan;29(1):89-99. doi: 10.1016/j.cjca.2012.07.847. Epub 2012 Oct 11. Can J Cardiol. 2013. PMID: 23062665 Review.
Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease.
Hu D, Hu D, Liu L, Barr D, Liu Y, Balderrabano-Saucedo N, Wang B, Zhu F, Xue Y, Wu S, Song B, McManus H, Murphy K, Loes K, Adler A, Monserrat L, Antzelevitch C, Gollob MH, Elliott PM, Barajas-Martinez H. Hu D, et al. Among authors: gollob mh. EBioMedicine. 2020 Apr;54:102723. doi: 10.1016/j.ebiom.2020.102723. Epub 2020 Apr 4. EBioMedicine. 2020. PMID: 32259713 Free PMC article.
Genetics of inherited primary arrhythmia disorders.
Spears DA, Gollob MH. Spears DA, et al. Among authors: gollob mh. Appl Clin Genet. 2015 Sep 18;8:215-33. doi: 10.2147/TACG.S55762. eCollection 2015. Appl Clin Genet. 2015. PMID: 26425105 Free PMC article. Review.
Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia.
Roberts JD, Gollob MH, Young C, Connors SP, Gray C, Wilton SB, Green MS, Zhu DW, Hodgkinson KA, Poon A, Li Q, Orr N, Tang AS, Klein GJ, Wojciak J, Campagna J, Olgin JE, Badhwar N, Vedantham V, Marcus GM, Kwok PY, Deo RC, Scheinman MM. Roberts JD, et al. Among authors: gollob mh. JACC Clin Electrophysiol. 2017 Mar;3(3):276-288. doi: 10.1016/j.jacep.2016.09.019. Epub 2016 Dec 21. JACC Clin Electrophysiol. 2017. PMID: 29759522 Free article.
169 results