يعرض 1 - 10 نتائج من 12 نتيجة بحث عن '"cardiomyopathy/si [Side Effect]"', وقت الاستعلام: 1.12s تنقيح النتائج
  1. 1
    مورد إلكتروني
  2. 2
    مورد إلكتروني

    URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/40046Test
    Journal of Medical Toxicology
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  3. 3
    مورد إلكتروني
  4. 4
    مورد إلكتروني
  5. 5
    مورد إلكتروني

    مصطلحات الفهرس: endometrium cancer/dt [Drug Therapy], enzyme inhibition, estrogen receptor positive breast cancer/dt [Drug Therapy], fatigue/si [Side Effect], gastrointestinal symptom/si [Side Effect], gene mutation, genetic transcription, human, hyperglycemia/si [Side Effect], hyperlipidemia/si [Side Effect], hypertension/si [Side Effect], hypoglycemia/si [Side Effect], hypophosphatemia/si [Side Effect], interstitial pneumonia/si [Side Effect], ischemic cardiomyopathy/si [Side Effect], kidney carcinoma/dt [Drug Therapy], lactic acidosis/si [Side Effect], lung non small cell cancer/dt [Drug Therapy], mantle cell lymphoma/dt [Drug Therapy], maximum tolerated dose, molecular interaction, mood disorder/si [Side Effect], mucosa inflammation/si [Side Effect], myeloma/dt [Drug Therapy], nausea/si [Side Effect], neoplasm, nonhuman, pancreas cancer/dt [Drug Therapy], pancreatic neuroendocrine tumor/dt [Drug Therapy], pharmacodynamics, phase 1 clinical trial (topic), priority journal, review, side effect/si [Side Effect], signal transduction, skin toxicity/si [Side Effect], solid tumor/dt [Drug Therapy], Streptomyces hygroscopicus, thrombocyte rich plasma, thrombocytopenia/si [Side Effect], treatment response, urogenital tract cancer/dt [Drug Therapy], uterine cervix cancer/dt [Drug Therapy], vomiting/si [Side Effect], 1 (1 cyano 1 methylethyl) 3 methyl 8 (3 quinolinyl)imidazo[4,5 c]quinolin 2(1h,3h) one/ct [Clinical Trial], 1 (1 cyano 1 methylethyl) 3 methyl 8 (3 quinolinyl)imidazo[4,5 c]quinolin 2(1h,3h) one/dt [Drug Therapy], 1 (1 cyano 1 methylethyl) 3 methyl 8 (3 quinolinyl)imidazo[4,5 c]quinolin 2(1h,3h) one/pd [Pharmacology], 2 (2 difluoromethylbenzimidazol 1 yl) 4,6 dimorpholino 1,3,5 triazine/ct [Clinical Trial], 2 (2 difluoromethylbenzimidazol 1 yl) 4,6 dimorpholino 1,3,5 triazine/pd [Pharmacology], 4 (4 amino 5 (7 methoxy 1h indol 2 yl)imidazo[5,1 f][1,2,4]triazin 7 yl)cyclohexanecarboxylic acid/ae [Adverse Drug Reaction], 4 (4 amino 5 (7 methoxy 1h indol 2 yl)imidazo[5,1 f][1,2,4]triazin 7 yl)cyclohexanecarboxylic acid/ct [Clinical Trial], 4 (4 amino 5 (7 methoxy 1h indol 2 yl)imidazo[5,1 f][1,2,4]triazin 7 yl)cyclohexanecarboxylic acid/pd [Pharmacology], 4 [2 (4 amino 1,2,5 oxadiazol 3 yl) 1 ethyl 7 (3 piperidinylmethoxy) 1h imidazo[4,5 c]pyridin 4 yl] 2 methyl 3 butyn 2 ol/ct [Clinical Trial], 4 [2 (4 amino 1,2,5 oxadiazol 3 yl) 1 ethyl 7 (3 piperidinylmethoxy) 1h imidazo[4,5 c]pyridin 4 yl] 2 methyl 3 butyn 2 ol/pd [Pharmacology], 4 diallylaminomethylene 1,3,4,7,10,11,12,13,14,15,16,17 dodecahydro 6 hydroxy 1 methoxymethyl 10,13 dimethyl 3,7,17 trioxo 2 oxacyclopenta[a]phenanthren 11 yl acetate/ae [Adverse Drug Reaction], 4 diallylaminomethylene 1,3,4,7,10,11,12,13,14,15,16,17 dodecahydro 6 hydroxy 1 methoxymethyl 10,13 dimethyl 3,7,17 trioxo 2 oxacyclopenta[a]phenanthren 11 yl acetate/ct [Clinical Trial], 4 diallylaminomethylene 1,3,4,7,10,11,12,13,14,15,16,17 dodecahydro 6 hydroxy 1 methoxymethyl 10,13 dimethyl 3,7,17 trioxo 2 oxacyclopenta[a]phenanthren 11 yl acetate/pd [Pharmacology], 1 (4 oxo 8 phenyl 4h 1 benzopyran 2 yl)morpholinio, azd 2014/ae [Adverse Drug Reaction], azd 2014/ct [Clinical Trial], azd 2014/dt [Drug Therapy], azd 2014/pk [Pharmacokinetics], azd 2014/pd [Pharmacology], azd 8055/ae [Adverse Drug Reaction], azd 8055/ct [Clinical Trial], azd 8055/dt [Drug Therapy], azd 8055/pd [Pharmacology], buparlisib/ae [Adverse Drug Reaction], buparlisib/ct [Clinical Trial], buparlisib/pd [Pharmacology], everolimus/ct [Clinical Trial], everolimus/dt [Drug Therapy], everolimus/pd [Pharmacology], interferon/cb [Drug Combination], interferon/dt [Drug Therapy], phosphatidylinositol 3 kinase inhibitor/ct [Clinical Trial], phosphatidylinositol 3 kinase inhibitor/dt [Drug Therapy], phosphatidylinositol 3 kinase inhibitor/iv [Intravenous Drug Administration], phosphatidylinositol 3 kinase inhibitor/po [Oral Drug Administration], phosphatidylinositol 3 kinase inhibitor/pk [Pharmacokinetics], phosphatidylinositol 3 kinase inhibitor/pd [Pharmacology], pictilisib/ae [Adverse Drug Reaction], pictilisib/ct [Clinical Trial], pictilisib/dt [Drug Therapy], pictilisib/pd [Pharmacology], ridaforolimus/ae [Adverse Drug Reaction], ridaforolimus/ct [Clinical Trial], ridaforolimus/pd [Pharmacology], temsirolimus/ct [Clinical Trial], temsirolimus/cb [Drug Combination], temsirolimus/dt [Drug Therapy], temsirolimus/pd [Pharmacology], unclassified drug, unindexed drug, xl 147/ae [Adverse Drug Reaction], xl 147/ct [Clinical Trial], xl 147/dt [Drug Therapy], xl 147/pd [Pharmacology], xl 765/ae [Adverse Drug Reaction], xl 765/ct [Clinical Trial], xl 765/pd [Pharmacology], azd 5363/ct [Clinical Trial], azd 5363/po [Oral Drug Administration], azd 5363/pd [Pharmacology], bay 80 6946/ae [Adverse Drug Reaction], bay 80 6946/ct [Clinical Trial], bay 80 6946/dt [Drug Therapy], bay 80 6946/iv [Intravenous Drug Administration], bay 80 6946/pd [Pharmacology], ds 7423/ct [Clinical Trial], gdc 0980/ae [Adverse Drug Reaction], gdc 0980/ct [Clinical Trial], gdc 0980/dt [Drug Therapy], gdc 0980/pd [Pharmacology], gsk 141795/ae [Adverse Drug Reaction], gsk 141795/ct [Clinical Trial], gsk 141795/pd [Pharmacology], gsk 2126458/ae [Adverse Drug Reaction], gsk 2126458/ct [Clinical Trial], gsk 2126458/dt [Drug Therapy], gsk 2126458/pd [Pharmacology], ink 128/ct [Clinical Trial], ink 128/dt [Drug Therapy], ink 128/pd [Pharmacology], ly 2780301/ct [Clinical Trial], ly 2780301/pk [Pharmacokinetics], ly 2780301/pd [Pharmacology], pf 04691502/ae [Adverse Drug Reaction], pf 04691502/ct [Clinical Trial], pf 04691502/dt [Drug Therapy], pf 04691502/po [Oral Drug Administration], pf 04691502/pd [Pharmacology], pki 587/ae [Adverse Drug Reaction], pki 587/ct [Clinical Trial], pki 587/dt [Drug Therapy], pki 587/iv [Intravenous Drug Administration], pki 587/pd [Pharmacology], pwt 33597/ct [Clinical Trial], pwt 33597/dt [Drug Therapy], pwt 33597/pd [Pharmacology], sar 254409/ae [Adverse Drug Reaction], sar 254409/ct [Clinical Trial], sar 254409/pd [Pharmacology], phase 3 clinical trial (topic), adrenal cortex carcinoma/dt [Drug Therapy], aminotransferase blood level, anorexia/si [Side Effect], bladder cancer/dt [Drug Therapy], breast cancer/dt [Drug Therapy], cancer chemotherapy, cancer survival, clinical trial (topic), diarrhea/si [Side Effect], drug dose escalation, drug dose increase, drug efficacy, drug eruption/si [Side Effect], drug intermittent therapy, Review

    URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/27530Test
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    LibKey Link

  6. 6
    مورد إلكتروني

    مصطلحات الفهرس: endometrium cancer/dt [Drug Therapy], enzyme inhibition, estrogen receptor positive breast cancer/dt [Drug Therapy], fatigue/si [Side Effect], gastrointestinal symptom/si [Side Effect], gene mutation, genetic transcription, human, hyperglycemia/si [Side Effect], hyperlipidemia/si [Side Effect], hypertension/si [Side Effect], hypoglycemia/si [Side Effect], hypophosphatemia/si [Side Effect], interstitial pneumonia/si [Side Effect], ischemic cardiomyopathy/si [Side Effect], kidney carcinoma/dt [Drug Therapy], lactic acidosis/si [Side Effect], lung non small cell cancer/dt [Drug Therapy], mantle cell lymphoma/dt [Drug Therapy], maximum tolerated dose, molecular interaction, mood disorder/si [Side Effect], mucosa inflammation/si [Side Effect], myeloma/dt [Drug Therapy], nausea/si [Side Effect], neoplasm, nonhuman, pancreas cancer/dt [Drug Therapy], pancreatic neuroendocrine tumor/dt [Drug Therapy], pharmacodynamics, phase 1 clinical trial (topic), priority journal, review, side effect/si [Side Effect], signal transduction, skin toxicity/si [Side Effect], solid tumor/dt [Drug Therapy], Streptomyces hygroscopicus, thrombocyte rich plasma, thrombocytopenia/si [Side Effect], treatment response, urogenital tract cancer/dt [Drug Therapy], uterine cervix cancer/dt [Drug Therapy], vomiting/si [Side Effect], 1 (1 cyano 1 methylethyl) 3 methyl 8 (3 quinolinyl)imidazo[4,5 c]quinolin 2(1h,3h) one/ct [Clinical Trial], 1 (1 cyano 1 methylethyl) 3 methyl 8 (3 quinolinyl)imidazo[4,5 c]quinolin 2(1h,3h) one/dt [Drug Therapy], 1 (1 cyano 1 methylethyl) 3 methyl 8 (3 quinolinyl)imidazo[4,5 c]quinolin 2(1h,3h) one/pd [Pharmacology], 2 (2 difluoromethylbenzimidazol 1 yl) 4,6 dimorpholino 1,3,5 triazine/ct [Clinical Trial], 2 (2 difluoromethylbenzimidazol 1 yl) 4,6 dimorpholino 1,3,5 triazine/pd [Pharmacology], 4 (4 amino 5 (7 methoxy 1h indol 2 yl)imidazo[5,1 f][1,2,4]triazin 7 yl)cyclohexanecarboxylic acid/ae [Adverse Drug Reaction], 4 (4 amino 5 (7 methoxy 1h indol 2 yl)imidazo[5,1 f][1,2,4]triazin 7 yl)cyclohexanecarboxylic acid/ct [Clinical Trial], 4 (4 amino 5 (7 methoxy 1h indol 2 yl)imidazo[5,1 f][1,2,4]triazin 7 yl)cyclohexanecarboxylic acid/pd [Pharmacology], 4 [2 (4 amino 1,2,5 oxadiazol 3 yl) 1 ethyl 7 (3 piperidinylmethoxy) 1h imidazo[4,5 c]pyridin 4 yl] 2 methyl 3 butyn 2 ol/ct [Clinical Trial], 4 [2 (4 amino 1,2,5 oxadiazol 3 yl) 1 ethyl 7 (3 piperidinylmethoxy) 1h imidazo[4,5 c]pyridin 4 yl] 2 methyl 3 butyn 2 ol/pd [Pharmacology], 4 diallylaminomethylene 1,3,4,7,10,11,12,13,14,15,16,17 dodecahydro 6 hydroxy 1 methoxymethyl 10,13 dimethyl 3,7,17 trioxo 2 oxacyclopenta[a]phenanthren 11 yl acetate/ae [Adverse Drug Reaction], 4 diallylaminomethylene 1,3,4,7,10,11,12,13,14,15,16,17 dodecahydro 6 hydroxy 1 methoxymethyl 10,13 dimethyl 3,7,17 trioxo 2 oxacyclopenta[a]phenanthren 11 yl acetate/ct [Clinical Trial], 4 diallylaminomethylene 1,3,4,7,10,11,12,13,14,15,16,17 dodecahydro 6 hydroxy 1 methoxymethyl 10,13 dimethyl 3,7,17 trioxo 2 oxacyclopenta[a]phenanthren 11 yl acetate/pd [Pharmacology], 1 (4 oxo 8 phenyl 4h 1 benzopyran 2 yl)morpholinio, azd 2014/ae [Adverse Drug Reaction], azd 2014/ct [Clinical Trial], azd 2014/dt [Drug Therapy], azd 2014/pk [Pharmacokinetics], azd 2014/pd [Pharmacology], azd 8055/ae [Adverse Drug Reaction], azd 8055/ct [Clinical Trial], azd 8055/dt [Drug Therapy], azd 8055/pd [Pharmacology], buparlisib/ae [Adverse Drug Reaction], buparlisib/ct [Clinical Trial], buparlisib/pd [Pharmacology], everolimus/ct [Clinical Trial], everolimus/dt [Drug Therapy], everolimus/pd [Pharmacology], interferon/cb [Drug Combination], interferon/dt [Drug Therapy], phosphatidylinositol 3 kinase inhibitor/ct [Clinical Trial], phosphatidylinositol 3 kinase inhibitor/dt [Drug Therapy], phosphatidylinositol 3 kinase inhibitor/iv [Intravenous Drug Administration], phosphatidylinositol 3 kinase inhibitor/po [Oral Drug Administration], phosphatidylinositol 3 kinase inhibitor/pk [Pharmacokinetics], phosphatidylinositol 3 kinase inhibitor/pd [Pharmacology], pictilisib/ae [Adverse Drug Reaction], pictilisib/ct [Clinical Trial], pictilisib/dt [Drug Therapy], pictilisib/pd [Pharmacology], ridaforolimus/ae [Adverse Drug Reaction], ridaforolimus/ct [Clinical Trial], ridaforolimus/pd [Pharmacology], temsirolimus/ct [Clinical Trial], temsirolimus/cb [Drug Combination], temsirolimus/dt [Drug Therapy], temsirolimus/pd [Pharmacology], unclassified drug, unindexed drug, xl 147/ae [Adverse Drug Reaction], xl 147/ct [Clinical Trial], xl 147/dt [Drug Therapy], xl 147/pd [Pharmacology], xl 765/ae [Adverse Drug Reaction], xl 765/ct [Clinical Trial], xl 765/pd [Pharmacology], azd 5363/ct [Clinical Trial], azd 5363/po [Oral Drug Administration], azd 5363/pd [Pharmacology], bay 80 6946/ae [Adverse Drug Reaction], bay 80 6946/ct [Clinical Trial], bay 80 6946/dt [Drug Therapy], bay 80 6946/iv [Intravenous Drug Administration], bay 80 6946/pd [Pharmacology], ds 7423/ct [Clinical Trial], gdc 0980/ae [Adverse Drug Reaction], gdc 0980/ct [Clinical Trial], gdc 0980/dt [Drug Therapy], gdc 0980/pd [Pharmacology], gsk 141795/ae [Adverse Drug Reaction], gsk 141795/ct [Clinical Trial], gsk 141795/pd [Pharmacology], gsk 2126458/ae [Adverse Drug Reaction], gsk 2126458/ct [Clinical Trial], gsk 2126458/dt [Drug Therapy], gsk 2126458/pd [Pharmacology], ink 128/ct [Clinical Trial], ink 128/dt [Drug Therapy], ink 128/pd [Pharmacology], ly 2780301/ct [Clinical Trial], ly 2780301/pk [Pharmacokinetics], ly 2780301/pd [Pharmacology], pf 04691502/ae [Adverse Drug Reaction], pf 04691502/ct [Clinical Trial], pf 04691502/dt [Drug Therapy], pf 04691502/po [Oral Drug Administration], pf 04691502/pd [Pharmacology], pki 587/ae [Adverse Drug Reaction], pki 587/ct [Clinical Trial], pki 587/dt [Drug Therapy], pki 587/iv [Intravenous Drug Administration], pki 587/pd [Pharmacology], pwt 33597/ct [Clinical Trial], pwt 33597/dt [Drug Therapy], pwt 33597/pd [Pharmacology], sar 254409/ae [Adverse Drug Reaction], sar 254409/ct [Clinical Trial], sar 254409/pd [Pharmacology], phase 3 clinical trial (topic), adrenal cortex carcinoma/dt [Drug Therapy], aminotransferase blood level, anorexia/si [Side Effect], bladder cancer/dt [Drug Therapy], breast cancer/dt [Drug Therapy], cancer chemotherapy, cancer survival, clinical trial (topic), diarrhea/si [Side Effect], drug dose escalation, drug dose increase, drug efficacy, drug eruption/si [Side Effect], drug intermittent therapy, Review

  7. 7
    مورد إلكتروني
  8. 8
    مورد إلكتروني

    مصطلحات الفهرس: chronic lung disease/pc [Prevention], chronic lung disease/th [Therapy], clinical trial, Cochrane Library, diet supplementation, disease association, diuresis, drug dose reduction, drug potentiation, duodenum perforation/si [Side Effect], echocardiography, electrolyte disturbance/si [Side Effect], evidence based medicine, family history, fiberoptic bronchoscopy, gastroduodenal ulcer/si [Side Effect], gastrointestinal symptom/dt [Drug Therapy], gastrointestinal symptom/pc [Prevention], genetic polymorphism, genetic predisposition, glucose intolerance/si [Side Effect], human, hypercalciuria/si [Side Effect], hypertension/si [Side Effect], hypertrophic obstructive cardiomyopathy/si [Side Effect], incidence, interstitial pneumonia, intrauterine infection, kidney calcification/si [Side Effect], leukomalacia/si [Side Effect], lipid diet, long term care, magnesium deficiency, meta analysis, monotherapy, nebulization, nephrolithiasis/si [Side Effect], newborn intensive care, oxygen therapy, oxygen toxicity/co [Complication], patent ductus arteriosus, pathogenesis, pertussis/dt [Drug Therapy], pertussis/pc [Prevention], positive end expiratory pressure, prematurity/dt [Drug Therapy], prematurity/pc [Prevention], prognosis, protein degradation, pulmonary hypertension/co [Complication], pulmonary hypertension/di [Diagnosis], pulmonary hypertension/dt [Drug Therapy], pulmonary hypertension/pc [Prevention], respiratory tract infection, retinol deficiency/dt [Drug Therapy], retinol deficiency/pc [Prevention], risk benefit analysis, secondary hyperparathyroidism/si [Side Effect], selenium deficiency, sepsis/si [Side Effect], side effect/si [Side Effect], systematic review, therapy delay, tidal volume, urea nitrogen blood level, virus infection/dt [Drug Therapy], beclometasone dipropionate/dt [Drug Therapy], bronchodilating agent/dt [Drug Therapy], chlorothiazide/cb [Drug Combination], chlorothiazide/dt [Drug Therapy], chlorothiazide/po [Oral Drug Administration], corticosteroid/cb [Drug Combination], corticosteroid/dt [Drug Therapy], dexamethasone/ae [Adverse Drug Reaction], dexamethasone/ct [Clinical Trial], dexamethasone/do [Drug Dose], dexamethasone/dt [Drug Therapy], dexamethasone/pd [Pharmacology], diuretic agent/cb [Drug Combination], diuretic agent/it [Drug Interaction], diuretic agent/dt [Drug Therapy], furosemide/ae [Adverse Drug Reaction], furosemide/cb [Drug Combination], furosemide/dt [Drug Therapy], furosemide/iv [Intravenous Drug Administration], furosemide/po [Oral Drug Administration], helium/dt [Drug Therapy], hydrochlorothiazide/cb [Drug Combination], hydrochlorothiazide/dt [Drug Therapy], hydrochlorothiazide/po [Oral Drug Administration], indometacin/ct [Clinical Trial], indometacin/dt [Drug Therapy], ipratropium bromide/dt [Drug Therapy], isoetarine/dt [Drug Therapy], isoprenaline/dt [Drug Therapy], nifedipine/dt [Drug Therapy], nifedipine/po [Oral Drug Administration], nitric oxide/dt [Drug Therapy], nitric oxide/ih [Inhalational Drug Administration], orciprenaline/dt [Drug Therapy], oxygen, pertussis vaccine/dt [Drug Therapy], protirelin/cb [Drug Combination], protirelin/dt [Drug Therapy], ranitidine/dt [Drug Therapy], ranitidine/iv [Intravenous Drug Administration], recombinant erythropoietin/dt [Drug Therapy], retinol/dt [Drug Therapy], ribavirin/dt [Drug Therapy], salbutamol/ae [Adverse Drug Reaction], salbutamol/ad [Drug Administration], salbutamol/dt [Drug Therapy], salbutamol/iv [Intravenous Drug Administration], salbutamol/po [Oral Drug Administration], sildenafil/dt [Drug Therapy], spironolactone/cb [Drug Combination], spironolactone/dt [Drug Therapy], spironolactone/po [Oral Drug Administration], steroid/ct [Clinical Trial], steroid/dt [Drug Therapy], steroid/ih [Inhalational Drug Administration], steroid/pd [Pharmacology], theophylline/cb [Drug Combination], theophylline/it [Drug Interaction], theophylline/dt [Drug Therapy], unindexed drug, uterus spasmolytic agent/dt [Drug Therapy], lung compliance, amino acid blood level, antioxidant activity, article, artificial ventilation, balloon dilatation, body weight disorder/si [Side Effect], bronchospasm, cardiovascular disease/si [Side Effect], cholelithiasis/si [Side Effect], chorioamnionitis, chronic lung disease/cn [Congenital Disorder], chronic lung disease/di [Diagnosis], chronic lung disease/dt [Drug Therapy], chronic lung disease/et [Etiology], Article

    URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/31781Test
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  9. 9
  10. 10
    مورد إلكتروني