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| 1 | Evidence for downy mildew races incucumber tested in Asia,Europe,and North America显示文摘 | SHETTY N V WEHNER T C THOMAS C E D0RUCH0WSKI RW VASANTH SHETTY K P | 2002 | ScientiaHorticulturae2002，94，3： | 1 |
| 2 | Linear and whorled ne- void hypermelanosis 显示文摘 | Mehta V Vasanth V Balachandran C | 2011 | Int J Dermatol2011，50，4： | 1 |
| 3 | Equilibrium, kinetics, mechanism, and process design for the sorption of methylene blue onto rice husk显示文摘 | VADIVELAN V VASANTH KUMAR K | 2005 | Journal of Colloid and Interface Science2005，286，： | 1 |
| 4 | Power Reduction Techniques for Mi-croprocessor System显示文摘 | Michael F | 2005 | ACM computing survey2005，37，3： | 1 |
| 5 | Power reduction techniques for microprocessor system 显示文摘 | V VASANTH F MICHAEL | 2005 | ACM computing survey2005，37，3： | 1 |
| 6 | Power reduction techniques formicroprocessor system显示文摘 | V Vasanth FMichael | 2005 | ACM computing survey2005，37，3： | 1 |
| 7 | Equilibrium,kinetics,mechanism,and process design for the sorption of methylene blue onto rice husk显示文摘 | Vadivelan V Vasanth K | 2005 | Journal of Colloid and Interface Science2005，286，1： | 1 |
| 8 | Emergence ofcarbapenem non -susceptible multidrug resistant Acineto-bacter baumannii strains of clonal coxplexes 103 (B) and92(B) harboring OXA-type carbapenemases and metallo-P-lactamases in Southern India显示文摘 | Saranathan R Vasanth V Vasanth Ty | 2015 | Microbiol Immunol2015，59，5： | 1 |
| 9 | Power reduction techniques for microprocessor system显示文摘 | F Michael | 2005 | ACM computing survey2005，37，3： | 1 |
| 10 | Nickel contact dermatitis from hypodermic needles显示文摘 | Mehta V Vasanth V Balachandran C | 2011 | Indian J Dermatol2011，56，： | 1 |
| 11 | Isolated sacral injuries: Postoperative length of stay, complications, and readmission显示文摘AIM: To investigate inpatient length of stay(LOS), complication rates, and readmission rates for sacral fracture patients based on operative approach.METHODS: All patients who presented to a large tertiary care center with isolated sacral fractures in an 11-year period were included in a retrospective chart review. Operative approach(open reduction internal fixation vs percutaneous) was noted, as well as age, gender, race, and American Society of Anesthesiologists' score. Complications included infection, nonunion and malunion, deep venous thrombosis, and hardware problems; 90-d readmissions were broken down into infection, surgical revision of the sacral fracture, and medical complications. LOS was collected for the initial admission and readmission visits if applicable. Fisher's exact and non-parametric t-tests(Mann-Whitney U tests) were employed to compare LOS, complications, and readmissions between open and percutaneous approaches.RESULTS: Ninety-four patients with isolated sacral fractures were identified: 31(30.4%) who underwentopen reduction and internal fixation(ORIF) vs 63(67.0%) who underwent percutaneous fixation. There was a significant difference in LOS based on operative approach: 9.1 d for ORIF patients vs 6.1 d for percutaneous patients(P = 0.043), amounting to a difference in cost of $13590. Ten patients in the study developed complications, with no significant difference in complication rates or reasons for complications between the two groups(19.4% for ORIF patients vs 6.3% for percutaneous patients). Eight patients were readmitted, with no significant difference in readmission rates or reasons for readmission between the two groups(9.5% percutaneous vs 6.5% ORIF).CONCLUSION: There is a significant difference in LOS based on operative approach for sacral fracture patients. Given similar complications and readmission rates, we recommend a percutaneous approach. | Vasanth Sathiyakumar Hanyuan Shi Rachel V Thakore Young M Lee David Joyce Jesse Ehrenfeld William T Obremskey Manish K Sethi | 2015 | World Journal of Orthopedics2015，6，8： | 0 |
| 12 | Floral extract of Tecoma stans:A potent inhibitor of gentamicin-induced nephrotoxicity in vivo显示文摘Objective:To highlight the nephroprotective activity of ethyl acetate extract of dried flowers of Tecomu stans for its protective effects on genlamicin-induced nephrotoxicity in albino rats. Methods:For studying acute toxicity study,single oral dose of 5(KM) mg ethyl acetate floral extract/kg hodv weight was administered to albino rats(five females,five males).Nephrotoxicity was induced in albino rats by intraperitoneal administration of gentamicin 80 mg/kg/day for eight days.Effect of concurrent administration of ethyl acetate floral extract of Tecoma stans at a dose of 100.200 and 300 mg/kg/day given by oral mute was determined using serum creatinine,serum uric acid,blood urea nitrogen and serum urea as indicators of kidney damage.The study groups contained six rats in each group.As nephrotoxicity of gentamicin is known to involve induction of oxidative stress,in vitro antioxidant aclivity and free radical-scavenging activity of this extract was also evaluated.Results:For acute toxicity testing both female and male rats administered with the extract at a dose of 5 000 mg/kg.The results showed no toxicity in terms of general behavior change,mortality,or change in gross appearance of internal organs(LD50>5 000 mg/kg). It was observed that the ethyl acetate floral extract of Tecoma stans significantly protected rat kidneys from gentamicin-induced histopathological changes.Gentamicin-induced glomerular congestion,peritubular and blood vessel congestion,epithelial desquamation,accumulation ol inflamnialoiy cells and necrosis of the kidney cells were found to be reduced in the groups receiving the ethyl acetate floral extract of Tecoma starts along with gentamicin in a dose dependent manner.The floral extract also reduced the gentamicin-induced increase in serum creatinine,serum uric acid,blood urea nitrogen and serum urea levels(P>0.01).Conclusions: The present study indicates a verv important role of reactive oxygen species(BOS) and the relation to renal dysfunction and point to the therapeutic potential of Tecoma stans in gentamicin induced nephrotoxicity. | Raju S Kavimani S Uma Maheshwara rao V Sreeramulu Reddy K Vasanth Kumar G | 2011 | Asian Pacific Journal of Tropical Medicine2011，4，9： | 0 |
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