Neural Networks and Rules-based Systems used to Find Rational and Scientific Correlations between being Here and Now with Afterlife Conditions
Neural Networks and Rules-based Systems used to Find Rational and
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This study was designed to assess short-term therapeutic effectiveness and psychological adverse effects of combination of pegylated interferon α-2a and ribavirin in Iraqi chronic hepatitis C patients. For this purpose fifty newly diagnosed chronic hepatitis C patients divided into three groups A, B and C, treated with equal doses of pegylated interferon α-2a (180 μg/week) and different doses of ribavirin (1200, 1000 and 800 mg/day respectively) and followed up for 12 weeks of starting treatment (prospective groups). Twenty healthy subjects were selected to be a normal group for the purpose of comparison. The results at week 12 (the time of achieving EVR) showed 100% complete EVR (cEVR) in group A, 4.4% cEVR and 5.6% null response in group B, 88.9% cEVR and 11.1% partial response in group C.
Dr. Vian Ahmed Wasta Ismael. 1970. \u201cEarly Virological Response of the First Line Combination Therapy (Pegylated Interferon I-2a and Ribavirin) in Iraqi Chronic Hepatitis C Patients and Their Psychological Adverse Effects\u201d. Unknown Journal GJMR Volume 12 (GJMR Volume 12 Issue 11): .
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Total Score: 112
Country: Iraq
Subject: Uncategorized
Authors: Dr. Vian Ahmed Wasta Ismael, Prof. Dr. Kassim Al-Shamma & Dr. Hiwa Abubakir Hussein (PhD/Dr. count: 2)
View Count (all-time): 132
Total Views (Real + Logic): 20904
Total Downloads (simulated): 11069
Publish Date: 1970 01, Thu
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Neural Networks and Rules-based Systems used to Find Rational and
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This study was designed to assess short-term therapeutic effectiveness and psychological adverse effects of combination of pegylated interferon α-2a and ribavirin in Iraqi chronic hepatitis C patients. For this purpose fifty newly diagnosed chronic hepatitis C patients divided into three groups A, B and C, treated with equal doses of pegylated interferon α-2a (180 μg/week) and different doses of ribavirin (1200, 1000 and 800 mg/day respectively) and followed up for 12 weeks of starting treatment (prospective groups). Twenty healthy subjects were selected to be a normal group for the purpose of comparison. The results at week 12 (the time of achieving EVR) showed 100% complete EVR (cEVR) in group A, 4.4% cEVR and 5.6% null response in group B, 88.9% cEVR and 11.1% partial response in group C.
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