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Manrique-Rodríguez S., de la Rubia-Nieto A., García-Robles J., Goicoechea-Diezhandino M., Gimeno-Blanes J., Pernía-López M., Pellicer-Franco C., Sanjurjo-Sáez M. Individualized therapy in patients with Fabry disease: is it a feasible strategy for rare diseases?. Expert Opinion on Orphan Drugs. 1 December 2016. 4:1199-1206. 10.1080/21678707.2016.1253468
AÑO: 2016; IF: 0.559
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Sabater-Molina M, Navarro M, García-Molina Sáez E, Garrido I, Pascual-Figal D, González Carrillo J, Gimeno Blanes JR. Mutation in JPH2 cause dilated cardiomyopathy. Clin Genet. 2016 Nov;90(5):468-469. doi: 10.1111/cge.12825. Epub 2016 Jul 29. PubMed PMID: 27471098.
AÑO: 2016; IF: 3.326
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Elliott P, Charron P, Blanes JR, Tavazzi L, Tendera M, Konté M, Laroche C, Maggioni AP; EORP Cardiomyopathy Registry Pilot Investigators. European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology. Eur Heart J. 2016 Jan 7;37(2):164-73. doi: 10.1093/eurheartj/ehv497. Epub 2015 Sep 25. PubMed PMID: 26409010.
AÑO: 2016; IF: 19.651
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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
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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
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