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Page 1
Genes frequently associated with sudden death in primary hypertrophic cardiomyopathy.
Herrera-Rodríguez DL, Totomoch-Serra A, Rosas-Madrigal S, Luna-Limón C, Marroquín-Ramírez D, Carnevale A, Rosendo-Gutiérrez R, Villarreal-Molina MT, Márquez-Murillo MF. Herrera-Rodríguez DL, et al. Among authors: rosendo gutierrez r. Arch Cardiol Mex. 2020;90(1):58-68. doi: 10.24875/ACM.19000294. Arch Cardiol Mex. 2020. PMID: 31996869 Free article. Review. English.
Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
Carnevale A, Rosas-Madrigal S, Rosendo-Gutiérrez R, López-Mora E, Romero-Hidalgo S, Avila-Vazzini N, Jacobo-Albavera L, Domínguez-Pérez M, Vargas-Alarcón G, Pérez-Villatoro F, Navarrete-Martínez JI, Villarreal-Molina MT. Carnevale A, et al. Among authors: rosendo gutierrez r. Mol Genet Genomic Med. 2020 Nov;8(11):e1504. doi: 10.1002/mgg3.1504. Epub 2020 Sep 24. Mol Genet Genomic Med. 2020. PMID: 32969603 Free PMC article.
Homozygous Fukutin Missense Mutation in Two Mexican Siblings with Dilated Cardiomyopathy.
Villarreal-mMolina MT, Rosas-Madrigal S, López-Mora E, Calderón-Avila AL, Rodríguez-Zanella H, Romero-Hidalgo S, Rosendo-Gutierrez R, Carnevale A. Villarreal-mMolina MT, et al. Among authors: rosendo gutierrez r. Rev Invest Clin. 2020 May 7;73(5). doi: 10.24875/RIC.20000277. Online ahead of print. Rev Invest Clin. 2020. PMID: 33048919 Free article.
Leukocyte Nuclear Morphology Alterations in Dilated Cardiomyopathy Caused by a Lamin AC Truncating Mutation (LMNA/Ser431*) Are Modified by the Presence of a LAP2 Missense Polymorphism (TMPO/Arg690Cys).
González-Garrido A, Rosas-Madrigal S, Rojo-Domínguez A, Arellanes-Robledo J, López-Mora E, Carnevale A, Arregui L, Rosendo-Gutiérrez R, Romero-Hidalgo S, Villarreal-Molina MT. González-Garrido A, et al. Among authors: rosendo gutierrez r. Int J Mol Sci. 2022 Nov 7;23(21):13626. doi: 10.3390/ijms232113626. Int J Mol Sci. 2022. PMID: 36362411 Free PMC article.