Last Posted: Aug 16, 2018
- Clinical Course and Management of Hypertrophic Cardiomyopathy.
Maron Barry J et al. The New England journal of medicine 2018 Aug (7) 655-668 - Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California.
Gallant N M et al. Molecular genetics and metabolism 2017 Nov 122(3) 76-84 - Challenges in the Diagnosis of Anderson-Fabry Disease: A Deceptively Simple and Yet Complicated Genetic Disease.
Marian Ali J et al. Journal of the American College of Cardiology 2016 68(10) 1051-3 - Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.
Nishiuchi Suguru et al. Circulation. Cardiovascular genetics 2017 Dec 10(6) - Genetics of Dilated Cardiomyopathy: Clinical Implications.
Paldino A et al. Current cardiology reports 2018 Aug 20(10) 83 - Genetics of hypertrophic cardiomyopathy: A review of current state.
Sabater-Molina M et al. Clinical genetics 2018 Jan 93(1) 3-14 - Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population.
Newman Randa et al. Pediatric cardiology 2018 Apr 39(4) 709-717 - Physical activity restriction for children and adolescents diagnosed with an inherited arrhythmia or cardiomyopathy and its impact on body mass index.
Christian Susan et al. Journal of cardiovascular electrophysiology 2018 Aug - Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease.
Pulignani Silvia et al. Pediatric cardiology 2018 Apr 39(4) 682-689 - Outcomes of Cardiac Screening in Adolescent Soccer Players.
Malhotra Aneil et al. The New England journal of medicine 2018 Aug (6) 524-534
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