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Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 67, Issue 20, pp. 2395 - 2410
Abstract Hydroxy-methyl-glutaryl-coenzyme A (HMG-CoA) reductase inhibitors or statins are well tolerated, but associated with various statin-associated... 
Cardiovascular | Internal Medicine | rhabdomyolysis | skeletal muscle | interstitial lung disease | myopathy | C-REACTIVE PROTEIN | RANDOMIZED CONTROLLED-TRIALS | CARDIAC & CARDIOVASCULAR SYSTEMS | FORCE 2014 UPDATE | PRIMARY-PREVENTION TRIAL | INDUCED MUSCLE TOXICITY | INTERSTITIAL LUNG-DISEASE | CENTRAL-NERVOUS-SYSTEM | OF-THE-LITERATURE | CORONARY-HEART-DISEASE | TYPE-2 DIABETES-MELLITUS | Liver Function Tests | Sleep Wake Disorders - chemically induced | Hydroxymethylglutaryl-CoA Reductase Inhibitors - immunology | Myalgia - chemically induced | Humans | Hyperlipidemias - drug therapy | Risk Factors | Lung Diseases, Interstitial - chemically induced | Tendon Injuries - chemically induced | Necrosis - chemically induced | Brain - drug effects | Rupture - chemically induced | Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects | Stroke - chemically induced | Cognition Disorders - etiology | Depression - chemically induced | Rhabdomyolysis - chemically induced | Antibodies - blood | Diabetes Mellitus - chemically induced | Acute Kidney Injury - chemically induced | Muscular Diseases - chemically induced | Testosterone - blood | Autoimmune Diseases - chemically induced | Hyperlipidemias - complications | Viral antibodies | Complications and side effects | Enzymes | Thiols | Antibodies | Diabetes | Cardiology | Statins | Cardiovascular agents | Creatine kinase | Muscles | Creatine | Respiratory tract diseases | Studies | Musculoskeletal system | Genotype & phenotype | Mortality | Clinical trials | Lipids | Clinical medicine
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 02/2014, Volume 63, Issue 7, pp. 630 - 635
Journal Article
European Journal of Gastroenterology & Hepatology, ISSN 0954-691X, 10/2018, Volume 30, Issue 10, pp. 1177 - 1186
OBJECTIVENew potent direct-acting antiviral (DAA) regimens against hepatitis C virus have been approved in recent years. However, information about the rate of... 
ribavirin | ledipasvir and sofosbuvir | hepatitis C virus | ombitasvir and dasabuvir | genotype 1 | adverse events | randomized | direct-acting antivirals | paritaprevir | ACUTE LIVER-FAILURE | VIRUS-INFECTION | SOFOSBUVIR | HCV INFECTION | REAL-WORLD EFFECTIVENESS | SUSTAINED VIROLOGICAL RESPONSE | DASABUVIR | GENOTYPE 1B CIRRHOSIS | RITONAVIR-BOOSTED PARITAPREVIR | GASTROENTEROLOGY & HEPATOLOGY | Anilides - adverse effects | Humans | Middle Aged | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Male | Fatigue - chemically induced | Drug Therapy, Combination - adverse effects | Ritonavir - adverse effects | Adult | Female | Fluorenes - adverse effects | Sofosbuvir - adverse effects | Benzimidazoles - adverse effects | Headache - chemically induced | Antiviral Agents - therapeutic use | Anemia - chemically induced | Genotype | Treatment Outcome | Macrocyclic Compounds - adverse effects | Hepatitis C, Chronic - drug therapy | Uracil - adverse effects | Ribavirin - adverse effects | Antiviral Agents - adverse effects | Sulfonamides - adverse effects | Carbamates - adverse effects | Viral Load - drug effects | Uracil - analogs & derivatives | Drugs | Antiviral agents | Complications and side effects | Treatment outcome | Usage | Analysis | Adverse and side effects | Hepatitis C | Drug therapy | Risk factors
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, p. e50778
Background: Hypoxia/reoxygenation(H/R)-induced apoptosis of cardiomyocytes plays an important role in myocardial injury. Lycopene is a potent antioxidant... 
ISCHEMIA-REPERFUSION INJURY | INFARCT SIZE | OXYGEN | INDUCED ACTIVATION | PATHWAY | MULTIDISCIPLINARY SCIENCES | DISEASE | CAROTENOIDS | ANEMIC RATS | AMERICAN-HEART-ASSOCIATION | CELL-DEATH | Animals, Newborn | Cell Survival - drug effects | Cell Hypoxia - drug effects | Mitochondrial Membrane Transport Proteins - chemistry | Mitochondrial Membrane Transport Proteins - metabolism | Myocytes, Cardiac - cytology | Apoptosis - drug effects | Mice, Inbred C57BL | Protein Conformation - drug effects | Mitochondria - metabolism | Mitochondria - drug effects | Carotenoids - pharmacology | Oxygen - metabolism | Animals | Myocytes, Cardiac - drug effects | Signal Transduction - drug effects | Cytoprotection - drug effects | Myocytes, Cardiac - metabolism | Mice | Oxidative Stress - drug effects | Cytochrome c | Infants (Newborn) | Antioxidants | Analysis | Heart cells | Permeability | Lycopene | Apoptosis | Cytochrome | Neonates | Reactive oxygen species | Heart attacks | Mitochondrial permeability transition pore | Membrane permeability | Cardiovascular disease | Activation | Caspase-3 | Neurotoxicity | Mitochondria | Reperfusion | Carotenoids | Ischemia | Rodents | Penicillin | Occupational health | Membrane potential | Pretreatment | Cardiology | Cardiovascular system | Caspase | Cardiomyocytes | Cultures | Pharmacology | Malondialdehyde | Hypotheses | Hospitals | Hypoxia | MPTP | Laboratory animals | Cytoplasm
Journal Article
Journal Article
Applied and Environmental Microbiology, ISSN 0099-2240, 09/2006, Volume 72, Issue 9, pp. 6111 - 6116
Journal Article
Journal Article
1985, ISBN 0774802200, xii, 168
Research into various aspects of the Holocaust has escalated in recent years just as the ranks of survivor-subjects are rapidly diminishing. All documents... 
Psychological aspects | Physiological aspects | Holocaust survivors | Bibliography |