Last Posted: Aug 08, 2019
- Assessing the barriers to cardiac care in carriers of Duchenne and Becker muscular dystrophy.
Eekhoff Lauren et al. Journal of genetic counseling 2019 Aug - A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes.
Park Joseph et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Aug - Using machine learning to predict one-year cardiovascular events in patients with severe dilated cardiomyopathy.
Chen Rui et al. European journal of radiology 2019 Aug 117178-183 - Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy.
Limongelli Giuseppe et al. International journal of cardiology 2019 Jul - Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project.
Machini Kalotina et al. American journal of human genetics 2019 Jul 105(1) 177-188 - Identification of Fabry Disease in a Tertiary Referral Cohort of Patients with Hypertrophic Cardiomyopathy.
Maron Martin S et al. The American journal of medicine 2018 131(2) 200.e1-200.e8 - Pathophysiology, diagnosis and management of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Study Group on peripartum cardiomyopathy.
Bauersachs Johann et al. European journal of heart failure 2019 Jun - Updates on the Genetic Paradigm in Heart Failure.
Rosenbaum Andrew N et al. Current treatment options in cardiovascular medicine 2019 Jun 21(8) 37 - A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy.
Catchpool Max et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jun - Genetic Testing and Cascade Screening in Pediatric Long QT Syndrome and Hypertrophic Cardiomyopathy.
Knight Linda M et al. Heart rhythm 2019 Jun
No hay comentarios:
Publicar un comentario