MARÍA ESPERANZA GARCÍA-MOLINA SÁEZ

García-Molina E, Sabater-Molina M, López-Cuenca D, Olmo MC, Pérez I, Muñoz Esparza C, Gimeno Blanes JR. A study of the pathogenicity of variants in familial heart disease. The value of cosegregation. Am J Transl Res. 2019 Mar 15;11(3):1724-1735. eCollection 2019. PubMed PMID: 30972196; PubMed Central PMCID: PMC6456527.

AÑO: 2019; IF: 3.375

30972196

Muñoz-Esparza C, Zorio E, Domingo Valero D, Peñafiel-Verdú P, Sánchez-Muñoz JJ, García-Molina E, Sabater M, Navarro M, San-Román I, Pérez I, Santos JJ, Cabañas-Perianes V, Valdés M, Pascual D, García-Alberola A, Gimeno Blanes JR. Value of the "Standing Test" in the Diagnosis and Evaluation of Beta-blocker Therapy Response in Long QT Syndrome. Rev Esp Cardiol (Engl Ed). 2017 Nov;70(11):907-914. doi: 10.1016/j.rec.2017.01.006. Epub 2017 Feb 21. English, Spanish. PubMed PMID: 28233664.

AÑO: 2017; IF: 5.166

28233664

Meca-Lallana, JE; Carreon-Guarnizo, E; Hernandez-Clares, R; Gomez-Espuch, J; Diaz-Perez, J; Garcia-Molina, E; Iniesta-Martinez, F; Perez-Aranda, A; Jimenez-Veiga, J; Zamarro-Parra, J; Leon-Hernandez, A; Velazquez-Marin, F; Martin-Fernandez, JJ. Recurrent immune thrombocytopenic purpura secondary to rituximab administered as neuromyelitis optica treatment: a case report presentation. MULTIPLE SCLEROSIS JOURNAL. 2017; 23:641-641.

AÑO: 2017; IF: 5.28

San Román I, Navarro M, Martínez F, Albert L, Polo L, Guardiola J, García-Molina E, Muñoz-Esparza C, López-Ayala JM, Sabater-Molina M, Gimeno JR. Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1. Clin Genet. 2016 Aug;90(2):171-6. doi: 10.1111/cge.12760. Epub 2016 Mar 23. PubMed PMID: 26857240.

AÑO: 2016; IF: 3.326

26857240

García-Molina E, Sabater-Molina M, Muñoz C, Ruiz-Espejo F, Gimeno JR. An R1632C variant in the SCN5A gene causing Brugada syndrome. Mol Med Rep. 2016 Jun;13(6):4677-80. doi: 10.3892/mmr.2016.5100. Epub 2016 Apr 11. PubMed PMID: 27082542.

AÑO: 2016; IF: 1.692

27082542