To study thecorrelation of thrombophilic polymorphism of Factor V Leiden (FV R506Q),Prothrombin gene mutation (G20210A) and Methylenetetrahydrofolate reductasegene (MTHFR C677T) mutation studies with type of cerebral palsy in children.
Best paper award for oral presentation on: Â“Glutathione-sÂ–transferase polymorphism and response to cyclophosphamide therapy in idiopathic nephrotic syndromeÂ” at 38th Annual Conference of Indian Society of Nephrology (ISNCON), 13-15th December 2007, New Delhi
Awarded the FIRST PRIZE for poster presentation entitled Â“De novo segmental duplication of 15q, confirmed by chromosomal microarray and FISH, in a child with global developmental delay and facial dysmorphismÂ” during the International Conference on Birth Defects 2014 & Symposium on Genetic Eye Diseases in Clinical Ophthalmology, Colombo, Sri Lanka; Â“Genes, Genome and Human MalformationsÂ” ; 9th Â– 11th February 2014
G Sharma, SV Attri, B Behra, S Bhisikar, PKumar, M Tageja, S Sharda, P Singhi, S Singhi. Analysis of 26 aminoacids in human plasma by HPLC using AQC as derivatizing agent and itsapplication in metabolic laboratory. Amino Acids, 2014. Feb 14: 1-11.Impact factor 3.914
Prasun P, Prasad N, Tripathi G, Jafar T, ShardaS, Gulati S, Agrawal S. Association of angiotensin-converting enzyme geneI/D polymorphism with steroid responsiveness in childhood nephrotic syndrome.Indian J Nephrol. 2011 Jan; 21(1):26-9
Panigrahi I, Das RR, Sharda S, MarwahaRK, Khandelwal N. Response to zolendronic acid in children with type IIIosteogenesis imperfecta. J Bone Miner Metab. 2010 Jul; 28(4):451-5.
Sharda SV, Gulati S, Tripathi G, Jafar T, Kumar A, Sharma RK, Agrawal S. Doglutathione-S-transferase polymorphisms influence response to intravenouscyclophosphamide therapy in idiopathic nephrotic syndrome? Pediatr Nephrol.2008 Nov; 23(11):2001-6
Sharda S, Phadke SR. Uptake of invasive prenatal diagnostic tests in womenafter detection of soft markers for chromosomal abnormality on ultrasonographicevaluation. J Perinatol. 2007 Sep; 27(9):550-5
ShardaS, Gilmour A, Harris V, Singh VP, Sinha N, Tewari S, Ramesh V, Agrawal S,Mastana S. Chemokine receptor 5 (CCR5) deletion polymorphism in North Indianpatients with coronary artery disease. Int J Cardiol. 2008 Feb 29;124(2):254-8
Girisha KM, Sharda SV, Phadke SR. Issuesin counseling for Down syndrome. Indian Pediatr. 2007 Feb; 44(2):131-3
Bajpai A, Kabra M, Gupta N, Sharda S,Ghosh M. Intravenous pamidronate therapy in osteogenesis imperfecta: responseto treatment and factors influencing outcome. J Pediatr Orthop. 2007 Mar;27(2):225-7
Dalal AB, Phadke SR, Pradhan M, Sharda S.Hemihyperplasia syndromes. Indian J Pediatr. 2006 Jul; 73(7):609-15
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