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Lopez-Sainz A, Dominguez F, Lopes LR, Ochoa JP, Barriales-Villa R, Climent V, Linschoten M, Tiron C, Chiriatti C, Marques N, Rasmussen TB, Espinosa MA, Beinart R, Quarta G, Cesar S, Field E, Garcia-Pinilla JM, Bilinska Z, Muir AR, Roberts AM, Santas E, Zorio E, Pena-Pena ML, Navarro M, Fernandez A, Palomino-Doza J, Azevedo O, Lorenzini M, Garcia-Alvarez MI, Bento D, Jensen MK, Mendez I, Pezzoli L, Sarquella-Brugada G, Campuzano O, Gonzalez-Lopez E, Mogensen J, Kaski JP, Arad M, Brugada R, Asselbergs FW, Monserrat L, Olivotto I, Elliott PM, Garcia-Pavia P; European Genetic Cardiomyopathies Initiative Investigators. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis. J Am Coll Cardiol. 2020 Jul 14;76(2):186-197. doi: 10.1016/j.jacc.2020.05.029. PubMed PMID: 32646569.
AÑO: 2020; IF: 24.094
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32646569
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Gil-Ortuno C, Sebastian-Marcos P, Sabater-Molina M, Nicolas-Rocamora E, Gimeno-Blanes JR, Fernandez Del Palacio MJ. Genetics of feline hypertrophic cardiomyopathy. Clin Genet. 2020 Sep;98(3):203-214. doi: 10.1111/cge.13743. Epub 2020 Apr 1. PubMed PMID: 32215921.
AÑO: 2020; IF: 4.438
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Casanova JD, Carrillo JG, Jimenez JM, Munoz JC, Esparza CM, Alvarez MS, Escriba R, Milla EB, de la Pompa JL, Raya A, Gimeno JR, Molina MS, Garcia GB. Trabeculated Myocardium in Hypertrophic Cardiomyopathy: Clinical Consequences. J Clin Med. 2020 Sep 30;9(10):3171. doi: 10.3390/jcm9103171. PubMed PMID: 33007916; PubMed Central PMCID: PMC7600439.
AÑO: 2020; IF: 4.241
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Garcia-Molina E, Sabater-Molina M, Lopez-Cuenca D, Olmo MC, Perez I, Munoz 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
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Ochoa JP, Sabater-Molina M, García-Pinilla JM, Mogensen J, Restrepo-Córdoba A, Palomino-Doza J, Villacorta E, Martinez-Moreno M, Ramos-Maqueda J, Zorio E, Peña-Peña ML, García-Granja PE, Rodríguez-Palomares JF, Cárdenas-Reyes IJ, de la Torre-Carpente MM, Bautista-Pavés A, Akhtar MM, Cicerchia MN, Bilbao-Quesada R, Mogollón-Jimenez MV, Salazar-Mendiguchía J, Mesa Latorre JM, Arnaez B, Olavarri-Miguel I, Fuentes-Cañamero ME, Lamounier A Jr, Pérez Ruiz JM, Climent-Payá V, Pérez-Sanchez I, Trujillo-Quintero JP, Lopes LR, Repáraz-Andrade A, Marín-Iglesias R, Rodriguez-Vilela A, Sandín-Fuentes M, Garrote JA, Cortel-Fuster A, Lopez-Garrido M, Fontalba-Romero A, Ripoll-Vera T, Llano-Rivas I, Fernandez-Fernandez X, Isidoro-García M, Garcia-Giustiniani D, Barriales-Villa R, Ortiz-Genga M, García-Pavía P, Elliott PM, Gimeno JR, Monserrat L. Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy. J Am Coll Cardiol. 2018 Nov 13;72(20):2457-2467. doi: 10.1016/j.jacc.2018.10.001. PubMed PMID: 30442288.
AÑO: 2018; IF: 18.639
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