Cardiomyopathy
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Last Posted: Aug 30, 2018
- Practice Variation among an International Group of Genetic Counselors on when to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy.
Christian S et al. Journal of genetic counseling 2018 Aug - When to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy The Family Perspective
S Christian et al, CIrc Genomics Prec Medicine, August 2018 - Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands.
Blusztein David I et al. Heart, lung & circulation 2018 Aug - Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals.
Myers Valerie D, et al. JAMA cardiology 2018 8 0. - Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM).
Hudson Janella et al. Journal of community genetics 2018 Aug - Using Decision Analysis to Support Newborn Screening Policy Decisions: A Case Study for Pompe Disease.
Prosser Lisa A et al. MDM policy & practice 2018 2018 - Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals
VD Myers, et al. JAMA Cardiology, August 22, 2018 - Translating emerging molecular genetic insights into clinical practice in inherited cardiomyopathies.
Asatryan Babken et al. Journal of molecular medicine (Berlin, Germany) 2018 Aug - 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
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