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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 1
2004 1
2006 2
2007 3
2008 2
2009 3
2010 2
2011 4
2013 2
2014 3
2015 1
2016 4
2017 1
2018 2
2019 2
2020 2
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2022 2
2023 1
2024 0

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Page 1
Patients with disorders of heart rhythm.
Nair M, Asirvatham SJ. Nair M, et al. Indian Heart J. 2011 Jul-Aug;63(4):305. Indian Heart J. 2011. PMID: 22497044 No abstract available.
Atrial flutter with atypical presentation.
Kataria V, Yaduvanshi A, Nair M. Kataria V, et al. Among authors: nair m. Indian Pacing Electrophysiol J. 2016 Mar-Apr;16(2):77-79. doi: 10.1016/j.ipej.2016.07.002. Epub 2016 Jul 15. Indian Pacing Electrophysiol J. 2016. PMID: 27676166 Free PMC article. No abstract available.
Why are clinical trials necessary in India?
Poongothai S, Unnikrishnan R, Balasubramanian J, Nair MD, Mohan V. Poongothai S, et al. Among authors: nair md. Perspect Clin Res. 2014 Apr;5(2):55-9. doi: 10.4103/2229-3485.128018. Perspect Clin Res. 2014. PMID: 24741480 Free PMC article.
Antithrombotic therapy in atrial fibrillation associated with valvular heart disease: a joint consensus document from the European Heart Rhythm Association (EHRA) and European Society of Cardiology Working Group on Thrombosis, endorsed by the ESC Working Group on Valvular Heart Disease, Cardiac Arrhythmia Society of Southern Africa (CASSA), Heart Rhythm Society (HRS), Asia Pacific Heart Rhythm Society (APHRS), South African Heart (SA Heart) Association and Sociedad Latinoamericana de Estimulación Cardíaca y Electrofisiología (SOLEACE).
Lip GYH, Collet JP, Caterina R, Fauchier L, Lane DA, Larsen TB, Marin F, Morais J, Narasimhan C, Olshansky B, Pierard L, Potpara T, Sarrafzadegan N, Sliwa K, Varela G, Vilahur G, Weiss T, Boriani G, Rocca B; ESC Scientific Document Group. Lip GYH, et al. Europace. 2017 Nov 1;19(11):1757-1758. doi: 10.1093/europace/eux240. Europace. 2017. PMID: 29096024 Review.
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: nair m. 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.
41 results