M. Santori

发表

Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths.

Á. Carracedo, F. Lotufo-Neto, M. Hirata, 2019, Forensic science international. Genetics.

Sarcomeric gene mutations in sudden infant death syndrome (SIDS).

R. Brugada, Á. Carracedo, B. Madea, 2012, Forensic science international.

Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS)

Á. Carracedo, B. Madea, M. Torres, 2009 .

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases

Á. Carracedo, L. Concheiro, C. Allegue, 2011, International Journal of Legal Medicine.

Novel Genomic Approach to the Arrhytmogenic Sudden Cardiac Death

Á. Carracedo, B. Sobrino, R. Gil, 2012 .

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders

Á. Carracedo, J. Amigo, B. Sobrino, 2014, Electrophoresis.

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation.

R. Brugada, Á. Carracedo, R. Gil, 2019, Forensic science international. Genetics.

Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood

Á. Carracedo, P. Schneider, J. Cortis, 2015, Archives of Disease in Childhood.

Prospective and Retrospective Diagnosis of Barth Syndrome Aided by Next-Generation Sequencing.

M. Couce, M. Santori, M. Brion, 2016, American journal of clinical pathology.