Movva S - Search Results

1

Trichohepatoenteric syndrome: founder mutation in asian indians.

Kotecha UH, Movva S, Puri RD, Verma IC. Kotecha UH, et al. Among authors: movva s. Mol Syndromol. 2012 Aug;3(2):89-93. doi: 10.1159/000339896. Epub 2012 Jul 5. Mol Syndromol. 2012. PMID: 23326254 Free PMC article.

2

Molecular evaluation of a novel missense mutation & an insertional truncating mutation in SUMF1 gene.

Kotecha UH, Movva S, Sharma D, Verma J, Puri RD, Verma IC. Kotecha UH, et al. Among authors: movva s. Indian J Med Res. 2014 Jul;140(1):55-9. Indian J Med Res. 2014. PMID: 25222778 Free PMC article.

3

Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India.

Bijarnia-Mahay S, Movva S, Gupta N, Sharma D, Puri RD, Kotecha U, Saxena R, Kabra M, Mohan N, Verma IC. Bijarnia-Mahay S, et al. Among authors: movva s. JIMD Rep. 2015;19:85-93. doi: 10.1007/8904_2014_374. Epub 2015 Jan 18. JIMD Rep. 2015. PMID: 25595217 Free PMC article.

4

KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1.

Vyas B, Puri RD, Namboodiri N, Nair M, Sharma D, Movva S, Saxena R, Bohora S, Aggarwal N, Vora A, Kumar J, Singh T, Verma IC. Vyas B, et al. Among authors: movva s. Am J Med Genet A. 2016 Jun;170(6):1510-9. doi: 10.1002/ajmg.a.37636. Epub 2016 Apr 4. Am J Med Genet A. 2016. PMID: 27041150 Review.

5

Genetic analysis of familial hypercholesterolemia in Asian Indians: A single-center study.

Setia N, Movva S, Balakrishnan P, Biji IK, Sawhney JPS, Puri R, Arora A, Puri RD, Saxena R, Mishra S, Apte S, Kulshrestha S, Ramprasad VL, Verma IC. Setia N, et al. Among authors: movva s. J Clin Lipidol. 2020 Jan-Feb;14(1):35-45. doi: 10.1016/j.jacl.2019.12.010. Epub 2020 Jan 9. J Clin Lipidol. 2020. PMID: 32044282

6

Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent in situ hybridization.

Eswarachari V, Kadam P, Movva S, Lingaiah S, Akther RM, Kidangan FX, Gowda KC, Golakoti RRK, Lall M, Mahajan S, Saviour P, Puri R, Verma IC, Vedam RL. Eswarachari V, et al. Among authors: movva s. J Matern Fetal Neonatal Med. 2019 Dec;32(24):4177-4180. doi: 10.1080/14767058.2018.1481383. Epub 2018 Jun 13. J Matern Fetal Neonatal Med. 2019. PMID: 29793366

7

Relationship of angiotensin-converting enzyme gene polymorphism with nephropathy associated with Type 2 diabetes mellitus in Asian Indians.

Movva S, Alluri RV, Komandur S, Vattam K, Eppa K, Mukkavali KK, Mubigonda S, Saharia S, Shastry JC, Hasan Q. Movva S, et al. J Diabetes Complications. 2007 Jul-Aug;21(4):237-41. doi: 10.1016/j.jdiacomp.2006.07.001. J Diabetes Complications. 2007. PMID: 17616353

8

Mitochondrial D310 instability in Asian Indian breast cancer patients.

Alhomidi MA, Vedicherla B, Movva S, Rao PK, Ahuja YR, Hasan Q. Alhomidi MA, et al. Among authors: movva s. Tumour Biol. 2013 Aug;34(4):2427-32. doi: 10.1007/s13277-013-0793-0. Epub 2013 May 3. Tumour Biol. 2013. PMID: 23640059

9

Association of methylene tetrahydrofolate reductase C677T genotype with type 2 diabetes mellitus patients with and without renal complications.

Movva S, Alluri RV, Venkatasubramanian S, Vedicherla B, Vattam KK, Ahuja YR, Hasan Q. Movva S, et al. Genet Test Mol Biomarkers. 2011 Apr;15(4):257-61. doi: 10.1089/gtmb.2010.0118. Epub 2010 Dec 27. Genet Test Mol Biomarkers. 2011. PMID: 21186995

10

Association of PON1 and APOA5 gene polymorphisms in a cohort of Indian patients having coronary artery disease with and without type 2 diabetes.

Bhaskar S, Ganesan M, Chandak GR, Mani R, Idris MM, Khaja N, Gulla S, Kumar U, Movva S, Vattam KK, Eppa K, Hasan Q, Pulakurthy UR. Bhaskar S, et al. Among authors: movva s. Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):507-12. doi: 10.1089/gtmb.2010.0207. Epub 2011 Mar 25. Genet Test Mol Biomarkers. 2011. PMID: 21438666

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