Works matching IS 00086312 AND DT 2017 AND VI 137 AND IP 2
Results: 11
Hypomethylation of the Angiotensin II Type I Receptor (AGTR1) Gene Along with Environmental Factors Increases the Risk for Essential Hypertension.
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- Cardiology, 2017, v. 137, n. 2, p. 126, doi. 10.1159/000458520
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- Publication type:
- Article
Discontinuation/Dose Reduction of Angiotensin-Converting Enzyme Inhibitors/Angiotensin Receptor Blockers during Acute Decompensated Heart Failure in African-American Patients with Reduced Left-Ventricular Ejection Fraction.
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- Cardiology, 2017, v. 137, n. 2, p. 121, doi. 10.1159/000457946
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- Publication type:
- Article
Strategies and Outcomes of Repeat Mitral Valve Interventions after Failed MitraClip Therapy.
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- Cardiology, 2017, v. 137, n. 2, p. 114, doi. 10.1159/000460240
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- Publication type:
- Article
Genotyping, Platelet Activation, and Cardiovascular Outcome in Patients after Percutaneous Coronary Intervention: Two Pieces of the Puzzle of Clopidogrel Resistance.
- Published in:
- Cardiology, 2017, v. 137, n. 2, p. 104, doi. 10.1159/000457947
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- Article
Wellen's Syndrome: A Bad Omen.
- Published in:
- 2017
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- Case Study
Resolution of Cheyne-Stokes Respiration after Treatment of Heart Failure with Sacubitril/Valsartan: A First Case Report.
- Published in:
- 2017
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- Publication type:
- Case Study
Sudden Cardiac Arrest Triggered by Coadministration of Fluconazole and Amiodarone.
- Published in:
- Cardiology, 2017, v. 137, n. 2, p. 92, doi. 10.1159/000455825
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- Publication type:
- Article
Predicting Successful Recanalization in Patients with Native Coronary Chronic Total Occlusion: The Busan CTO Score.
- Published in:
- Cardiology, 2017, v. 137, n. 2, p. 83, doi. 10.1159/000455824
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- Publication type:
- Article
Exome Sequencing Identifies a Novel DES Mutation (R227C) in a Chinese Dilated Cardiomyopathy Family.
- Published in:
- Cardiology, 2017, v. 137, n. 2, p. 78, doi. 10.1159/000455181
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- Publication type:
- Article
Tafamidis for the Treatment of Hereditary Transthyretin Amyloid Cardiomyopathy: A Case Report.
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- Cardiology, 2017, v. 137, n. 2, p. 74, doi. 10.1159/000455089
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- Publication type:
- Article
Mild Left Ventricular Hypertrophy Unravels a Novel Nonsense Mutation of the GLA Gene Associated with the Classical Phenotype of Fabry Disease.
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- Cardiology, 2017, v. 137, n. 2, p. 67, doi. 10.1159/000455117
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- Publication type:
- Article