Last Posted: Apr 11, 2019
- A Genetic Score of Predisposition to Low-Grade Inflammation Associated with Obesity May Contribute to Discern Population at Risk for Metabolic Syndrome.
Galmés Sebastià et al. Nutrients 2019 Jan 11(2) - ESC e-Cardiology Working Group Position Paper: Overcoming challenges in digital health implementation in cardiovascular medicine.
Frederix Ines et al. European journal of preventive cardiology 2019 Mar 2047487319832394 - Accurate and rapid screening model for potential diabetes mellitus.
Pei Dongmei et al. BMC medical informatics and decision making 2019 Mar 19(1) 41 - Development and Evaluation of a Mobile Decision Support System for Hypertension Management in the Primary Care Setting in Brazil: Mixed-Methods Field Study on Usability, Feasibility, and Utility.
Silveira Daniel Vitório et al. JMIR mHealth and uHealth 2019 Mar 7(3) e9869 - The Association Between Medication Adherence for Chronic Conditions and Digital Health Activity Tracking: Retrospective Analysis.
Quisel Tom et al. Journal of medical Internet research 2019 Mar 21(3) e11486 - Genetics Of Atrial Fibrilation: In Search Of Novel Therapeutic Targets.
Lozano-Velasco Estefanía et al. Cardiovascular & hematological disorders drug targets 2019 Feb - Gene and environmental interactions according to the components of lifestyle modifications in hypertension guidelines.
Kokubo Yoshihiro et al. Environmental health and preventive medicine 2019 Mar 24(1) 19 - Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.
Breil Thomas et al. Journal of pediatric endocrinology & metabolism : JPEM 2019 Feb - [Pulmonary arterial hypertension as leading manifestation of methylmalonic aciduria: clinical characteristics and gene testing in 15 cases].
Liu X Q et al. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2017 49(5) 768-777 - Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations.
Regalado Ellen S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(10) 1206-1215
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