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| 1 | Quantification of fragments of human serum inter-α-trypsin inhibitor heavy chain 4 by a surface-enhanced laser desorption/ionization-based immunoassay显示文摘 | Jin S Manisha P | 2006 | Clinical Chemistry2006，52，： | 1 |
| 2 | Synthesis of 4-aryl aubstituted 3,4-Dihydropyrimidinones using silica-cldoride under solvent free conditions显示文摘 | HITENDRA N K MANISHA S KAUSHIK M P | 2007 | Molecules2007，12，： | 1 |
| 3 | R-Facter in Salmonella enteria serovar Typhi: transfer to and acquisition from Escherichia coli 显示文摘 | Shyamapada M Manisha D M Nishith K P | 2003 | Jpn J Infect Dis2003，，56： | 1 |
| 4 | Superinfection of hepatitis E Virus as a cause of decompensation in liver cirrhosis due to hepatitis B virus显示文摘Objevtive:Super infection with hepatitis A virus(HAV ) and hepatitis E virus(HEV ) in the presence of underlying hepatocellular injury can cause severe illness.In endemic areas such as India,however most patients already have been exposed to HAV but could still be susceptible to HEV infection.In our study we determined the seroprevalence of anti-HAV IgM and anti-HEV IgM to assess the incidence of superinfection with these viruses in cirrhotic patients with the goal of defining the need for protection against these viruses and further correlate the presence of these viruses with the clinical course.Methods:We studied 53 patients of cirrhosis as a result of Hepatitis B virus.Apparent causes of decompensation were ruled out before their inclusion in the study group.Serum sample from these patients was tested for HBsAg,anti HBc IgG,anti HEV IgM and anti HAV IgG and IgM by commercially available ELISA kit.Liver function test was done on all the patients and correlated with various serological markers.Results:anti HBc IgG was present in all the cases of cirrhosis. Hepatitis B surface antigen was present in 20 out of 53 cases of cirrhosis.None of the patients demonstrated anti-HAV IgM,however one patient had anti-HEV IgM.Conclusion:Superinfection with HAV in adult patient is uncommon in India.Prevalence of acute HEV infection in decompensated cirrhosis is low in the present study but presence of HEV superinfection in one patient corroborates the apprehension of liver function deterioration following superinfection with HEV virus. | Manisha Jain Anita Chakravarti P Kar Mbbs Md | 2009 | Asian Pacific Journal of Tropical Medicine2009，2，2： | 1 |
| 5 | Glycerol as a reference material for fecal fat quantitation using low- resolution time domain 1H NMR spectroscopy显示文摘 | JAMES P C JUDY S MANISHA S | 2011 | Clinical Biochemistry2011，44，16： | 1 |
| 6 | Effects of Gellant Concentration on the Burning and Flame Structure of Organic Gel Propellant Droplets 显示文摘 | Mishra D P Advitya Patyal Manisha Padhwal | 2011 | Fuel2011，90，5： | 1 |
| 7 | Kinetics of heterogeneous oxidation of benzyl alcohol withhydrogen peroxide显示文摘 | MANISHA P CHAUDHARI SUDHIRPRAKASH B SAWANT | 2005 | Chemical Engineering Journal2005，，106： | 1 |
| 8 | Suspected twin-twin transfusion syndrome: How often is the diagnosis correct and referral timely显示文摘 | Manisha G Ramesha P Michael T | 2012 | Ultrasound Med2012，31，： | 1 |
| 9 | Hydrothermal and biotechnological treatments on nutraceutical content and antioxidant activity of rice bran显示文摘 | Pradeep P M Jayadeep A Manisha G | 2014 | Journal of Cereal Science2014，60，1： | 1 |
| 10 | Development ofmeloxicam formulations utilizing ternary complexationfor solubility enhancement显示文摘 | Awasthi SS Kumar TG Manisha P | 2011 | Pak J Pharm Sci2011，24，4： | 1 |
| 11 | Synthesis and molecular modeling studies of 3-chloro-4-sub- stituted-1 - ( 8 -hydroxy-quinolin-5-yl) azetidin-2 -ones as novel anti-filarial agents 显示文摘 | Chhajed S S Manisha P Bastikar V A | 2010 | Bioorg Med Chem Lett2010，20，12： | 1 |
| 12 | Combined administration of a chelating agent ,and an antioxidant in the prevention and treatment of acute lead intoxication in rats显示文摘 | Manisha Pande Ashish Mehta Bhagwat P | 2001 | Environmental Toxicology and Pharnaeology2001，9，： | 1 |
| 13 | Combined administration of a chelating agent and an antioxidant in the prevention and treatment of acute lead intoxication in rats显示文摘 | Manisha Pande Ashish Mehta Bhagwat P | 2001 | Environmental Toxicology and Phamacology2001，9，： | 1 |
| 14 | Beneficial effects of high dietary fiber intake in patients with type 2 diabetes mellitus显示文摘 | Manisha Chandalia M D Abhimanyu Garg M D Dieter Lutjohann P D | 2000 | The New England Journal of Medicine2000，342，19： | 1 |
| 15 | A validated specific reverse phase liquid chromatographic method for the determination of valacyclovir in the presence of its degradation products in bulk drug and in tablet dosage form 显示文摘 | PATIL G D YEOLE P G MANISHA P | 2009 | Int J Chem Tech Res2009，1，1： | 1 |
| 16 | Circulating cell free DNA in plasma/Serum of lung cancer patients as a potential screening and prognostic tool显示文摘 | ASHUTOSH K P MANISHA B SACHIN K | 2006 | Clin Chem2006，52，10： | 1 |
| 17 | Past, present and future of kidney paired donation transplantation in India显示文摘One third of healthy willing living kidney donors are rejected due to ABO blood group incompatibility and donor specific antibody. This increases pre-transplant dialysis duration leading to increased morbidity and mortality on the kidney transplantation waiting list. Over the last decade kidney paired donation is most rapidly increased source of living kidney donors. In a kidney transplantation program dominated by living donor kidney transplantation, kidney paired donation is a legal and valid alternative strategy to increase living donor kidney transplantation. This is more useful in countries with limited resources where ABO incompatible kidney transplantation or desensitization protocol is not feasible because of costs/infectious complications and deceased donor kidney transplantation is in initial stages. The matching allocation, ABO blood type imbalance, reciprocity, simultaneity, geography were the limitation for the expansion of kidney paired donation. Here we describe different successful ways to increase living donor kidney transplantation through kidney paired donation. Compatible pairs, domino chain, combination of kidney paired donation with desensitization or ABO incompatible transplantation, international kidney paired donation, nonsimultaneous, extended, altruistic donor chain and list exchange are different ways to expand the donor pool.In absence of national kidney paired donation program,a dedicated kidney paired donation team will increase access to living donor kidney transplantation in individual centres with team work. Use of social networking sites to expand donor pool, HLA based national kidney paired donation program will increase quality and quantity of kidney paired donation transplantation. Transplant centres should remove the barriers to a broader implementation of multicentre, national kidney paired donation program to further optimize potential of kidney paired donation to increase transplantation of O group and sensitized patients. This review assists in the development of similar programs in other developing countries. | Vivek B Kute Himanshu V Patel Pankaj R Shah Pranjal R Modi Veena R Shah Sayyed J Rizvi Bipin C Pal Manisha P Modi Priya S Shah Umesh T Varyani Pavan S Wakhare Saiprasad G Shinde Vijay A Ghodela Minaxi H Patel Varsha B Trivedi Hargovind L Trivedi | 2017 | World Journal of Transplantation2017，7，2： | 0 |
| 18 | Increasing access to kidney transplantation for sensitized recipient through three-way kidney paired donation with desensitization: The first Indian report显示文摘The combination of kidney paired donation(KPD) with desensitization represents a promising method of increasing the rate of living donor kidney transplantation(LDKT) in immunologically challenging patients. Patients who are difficult to match and desensitize due to strong donor specific antibody are may be transplanted by a combination of desensitization and KPD protocol with more immunologically favorable donor. We present our experience of combination of desensitization protocol with three-way KPD which contributed to successful LDKT in highly sensitized end stage renal disease patient. All recipients were discharged with normal and stable allograft function at 24 mo follow up. We believe that this is first report from India where three-way KPD exchange was performed with the combination of KPD and desensitization. The combination of desensitization protocol with KPD improves access and outcomes of LDKT. | Vivek B Kute Himanshu V Patel Pankaj R Shah Pranjal R Modi Veena R Shah Sayyed J Rizvi Bipin C Pal Manisha P Modi Priya S Shah Umesh T Varyani Pavan S Wakhare Saiprasad G Shinde Viajay A Ghodela Minaxi H Patel Varsha B Trivedi Hargovind L Trivedi | 2016 | World Journal of Clinical Cases2016，4，10： | 0 |
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