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The New England journal of medicine, ISSN 1533-4406, 2016, Volume 375, Issue 12, pp. 1131 - 1141
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2019, Volume 380, Issue 14, pp. 1326 - 1335
Journal Article
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 2018, Volume 141, Issue 1, pp. 110 - 116.e7
Background Significant adverse effects (AEs) have been associated with continuous exposure to oral corticosteroids (OCSs). The potential association with... 
Allergy and Immunology | adverse effects | severe asthma | Oral corticosteroids | burst therapy | UNITED-STATES | EVENTS | ALLERGY | DOSE-RESPONSE RELATIONSHIP | INHALED CORTICOSTEROIDS | COMPLICATIONS | IMMUNOLOGY | Cataract - chemically induced | Humans | Middle Aged | Fractures, Bone - epidemiology | Male | Cataract - epidemiology | Gastrointestinal Hemorrhage - epidemiology | Diabetes Mellitus, Type 2 - epidemiology | Hypertension - chemically induced | Adult | Female | Retrospective Studies | Hypertension - epidemiology | Asthma - epidemiology | Osteoporosis - epidemiology | Obesity - chemically induced | Osteoporosis - chemically induced | Administration, Oral | Asthma - drug therapy | Adrenal Cortex Hormones - adverse effects | Gastrointestinal Hemorrhage - chemically induced | Obesity - epidemiology | Diabetes Mellitus, Type 2 - chemically induced | Fractures, Bone - chemically induced | Adrenal Cortex Hormones - administration & dosage | Cataracts | Corticoids | Glaucoma | Systematic review | Metabolic syndrome | Bleeding | Osteoporosis | Biomedical materials | Immunology | Databases | Biocompatibility | Drug dosages | Chronic illnesses | Hypertension | Corticosteroids | Medicare | Diabetes mellitus | Exposure | Patients | Allergies | Asthma | Studies | Side effects | Fractures | Tuberculosis | Ulcers | Diabetes
Journal Article
Journal Article
The lancet oncology, ISSN 1470-2045, 2017, Volume 18, Issue 5, pp. 640 - 653
Summary Background Although trastuzumab plus chemotherapy is the standard of care for first-line treatment of HER2-positive advanced gastric cancer, there is... 
Hematology, Oncology and Palliative Medicine | SURVIVAL | SUPPORTIVE CARE | WEEKLY PACLITAXEL | ONCOLOGY | 2ND-LINE CHEMOTHERAPY | IRINOTECAN | LEVEL | PLUS PACLITAXEL | HER2 | CANCER | DOCETAXEL | Follow-Up Studies | Febrile Neutropenia - chemically induced | Humans | Middle Aged | Male | Stomach Neoplasms - pathology | Antineoplastic Agents - therapeutic use | Taxoids - therapeutic use | Antineoplastic Agents - adverse effects | Pneumonia - chemically induced | Aged, 80 and over | Adult | Female | Stomach Neoplasms - chemistry | Adenocarcinoma - chemistry | Taxoids - adverse effects | Antibodies, Monoclonal, Humanized - adverse effects | Maytansine - adverse effects | Bridged-Ring Compounds - therapeutic use | Antibodies, Monoclonal, Humanized - therapeutic use | Maytansine - analogs & derivatives | Anemia - chemically induced | Survival Rate | Thrombocytopenia - chemically induced | Stomach Neoplasms - drug therapy | Maytansine - therapeutic use | Adenocarcinoma - drug therapy | Adenocarcinoma - secondary | Esophagogastric Junction | Gastrointestinal Hemorrhage - chemically induced | Retreatment | Intention to Treat Analysis | Bridged-Ring Compounds - adverse effects | Aged | Receptor, ErbB-2 - analysis | Trastuzumab | Adenocarcinoma | Medical research | Chemotherapy | Clinical trials | Medicine, Experimental | Metastasis | Esophageal cancer | Cancer | Analysis
Journal Article
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2011, Volume 141, Issue 4, pp. 1314 - 1322.e5
..., a primary role of cyclooxygenase (COX) inhibition in the mechanism of NSAID-induced enteropathy is not clear. On the other hand, the enterohepatic recirculation... 
Gastroenterology and Hepatology | Ulcer | Microflora | Bleeding | Acid Secretion | ULCERS | NONSTEROIDAL ANTIINFLAMMATORY DRUG | PERMEABILITY | RATS | INDOMETHACIN | LEUKOCYTE ADHERENCE | INDUCED GASTRIC DAMAGE | PATHOGENESIS | NITRIC-OXIDE | BACTERIAL OVERGROWTH | GASTROENTEROLOGY & HEPATOLOGY | Jejunum - pathology | Rats, Wistar | Colon - drug effects | Hematocrit | Peptic Ulcer - prevention & control | Male | Omeprazole - toxicity | Bifidobacterium - isolation & purification | Bifidobacterium - growth & development | Actinobacteria - drug effects | Jejunum - drug effects | Drug Interactions | Peptic Ulcer - microbiology | Time Factors | Actinobacteria - genetics | Actinobacteria - isolation & purification | Disease Models, Animal | Bifidobacterium - genetics | Jejunum - microbiology | Rats | Celecoxib | Probiotics - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Proton Pump Inhibitors - toxicity | Anti-Inflammatory Agents, Non-Steroidal - toxicity | Peptic Ulcer - pathology | Denaturing Gradient Gel Electrophoresis | 2-Pyridinylmethylsulfinylbenzimidazoles - toxicity | Gastrointestinal Hemorrhage - chemically induced | Gastrointestinal Hemorrhage - prevention & control | Bifidobacterium - drug effects | Animals | Gastrointestinal Hemorrhage - microbiology | Actinobacteria - growth & development | Pyrazoles - toxicity | Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics | Naproxen - toxicity | Sulfonamides - toxicity | Colon - microbiology | Peptic Ulcer - chemically induced | Gastrointestinal Hemorrhage - pathology | Lansoprazole | Proton pump inhibitors | Messenger RNA | Nonsteroidal anti-inflammatory drugs
Journal Article
The Lancet (British edition), ISSN 0140-6736, 2017, Volume 390, Issue 10093, pp. 490 - 499
Journal Article