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Revista Espanola De Cardiologia (English Ed.)|April 11, 2018
Insights Into Hypertrophic Cardiomyopathy Evaluation Through Follow-up of a Founder Pathogenic VariantRebeca Lorca, Juan Gómez, María Martín, et al.Journal of Molecular Neuroscience : MN|March 23, 2011
Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's diseaseAna Miar, Victoria Alvarez, Ana I Corao, et al.Clinical Chemistry|July 26, 2003
Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patientsMónica García-Castro, Julián R Reguero, Alberto Batalla, et al.Neuroscience Letters|May 3, 2005
Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonismIgnacio F Mata, Victoria Alvarez, Eliecer Coto, et al.Epigenomics|July 3, 2018
Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathyJuan Gómez, Rebeca Lorca, Julián R Reguero, et al.Genetic Testing and Molecular Biomarkers|August 31, 2016
Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian PatientsNawel Jaafar, Juan Gómez, Ikram Kammoun, et al.Journal of Clinical Medicine|February 10, 2024
Influence of the HLA-Cw6 Allele and IFIH1/MDA5 Gene Variants on the Cardiometabolic Risk Profile of Patients with Psoriatic DiseaseRubén Queiro, Ignacio Braña, Estefanía Pardo, et al.Kidney International|July 9, 2003
A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigreesSandro Rossetti, Roser Torra, Eliecer Coto, et al.Journal of the Neurological Sciences|June 25, 2005
Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish populationCecilia Huerta, Mónica G Castro, Eliecer Coto, et al.Molecular Biology Reports|June 22, 2012
New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathyCristina Alonso-Montes, Manuel Naves-Diaz, Jose Luis Fernandez-Martin, et al.Pageof 23