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

Year Number of Results
1993 1
1996 1
2005 1
2009 2
2010 1
2011 5
2012 1
2013 8
2014 5
2015 8
2016 7
2017 7
2018 6
2019 4
2020 4
2021 11
2022 0
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65 results
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Page 1
Huppke-Brendel Syndrome.
Bindu PS, Chiplunkar S, Vandana VP, Nagappa M, Govindaraj P, Taly A. Bindu PS, et al. Among authors: govindaraj p. 2019 Jun 13. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2019 Jun 13. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 31194315 Free Books & Documents. Review.
Child Neurology: Ethylmalonic encephalopathy.
Govindaraj P, Parayil Sankaran B, Nagappa M, Arvinda HR, Deepha S, Jessiena Ponmalar JN, Sinha S, Gayathri N, Taly AB. Govindaraj P, et al. Neurology. 2020 Mar 24;94(12):e1336-e1339. doi: 10.1212/WNL.0000000000009144. Epub 2020 Feb 28. Neurology. 2020. PMID: 32111695 No abstract available.
Mitochondrial disorders: challenges in diagnosis & treatment.
Khan NA, Govindaraj P, Meena AK, Thangaraj K. Khan NA, et al. Among authors: govindaraj p. Indian J Med Res. 2015 Jan;141(1):13-26. doi: 10.4103/0971-5916.154489. Indian J Med Res. 2015. PMID: 25857492 Free PMC article. Review.
Mitochondrial genome variations in idiopathic dilated cardiomyopathy.
Govindaraj P, Rani B, Sundaravadivel P, Vanniarajan A, Indumathi KP, Khan NA, Dhandapany PS, Rani DS, Tamang R, Bahl A, Narasimhan C, Rakshak D, Rathinavel A, Premkumar K, Khullar M, Thangaraj K. Govindaraj P, et al. Mitochondrion. 2019 Sep;48:51-59. doi: 10.1016/j.mito.2019.03.003. Epub 2019 Mar 22. Mitochondrion. 2019. PMID: 30910572
Child Neurology: Hereditary Folate Malabsorption.
Huddar A, Chiplunkar S, Nagappa M, Govindaraj P, Sinha S, Taly AB, Sankaran BP. Huddar A, et al. Among authors: govindaraj p. Neurology. 2021 Jul 6;97(1):40-43. doi: 10.1212/WNL.0000000000012083. Epub 2021 Apr 23. Neurology. 2021. PMID: 33893200 No abstract available.
Leukodystrophy Due to eIF2B Mutations in Adults.
Shivaram S, Nagappa M, Seshagiri DV, Saini J, Govindaraj P, Sinha S, Bindu PS, Taly AB. Shivaram S, et al. Among authors: govindaraj p. Can J Neurol Sci. 2021 Sep 2:1-5. doi: 10.1017/cjn.2021.202. Online ahead of print. Can J Neurol Sci. 2021. PMID: 34663487
Genome-wide analysis correlates Ayurveda Prakriti.
Govindaraj P, Nizamuddin S, Sharath A, Jyothi V, Rotti H, Raval R, Nayak J, Bhat BK, Prasanna BV, Shintre P, Sule M, Joshi KS, Dedge AP, Bharadwaj R, Gangadharan GG, Nair S, Gopinath PM, Patwardhan B, Kondaiah P, Satyamoorthy K, Valiathan MV, Thangaraj K. Govindaraj P, et al. Sci Rep. 2015 Oct 29;5:15786. doi: 10.1038/srep15786. Sci Rep. 2015. PMID: 26511157 Free PMC article.
PMP22 Gene-Associated Neuropathies: Phenotypic Spectrum in a Cohort from India.
Nagappa M, Sharma S, Govindaraj P, Chickabasaviah YT, Siram R, Shroti A, Debnath M, Sinha S, Bindu PS, Taly AB. Nagappa M, et al. Among authors: govindaraj p. J Mol Neurosci. 2020 May;70(5):778-789. doi: 10.1007/s12031-020-01488-w. Epub 2020 Jan 28. J Mol Neurosci. 2020. PMID: 31993930
RAF1 mutations in childhood-onset dilated cardiomyopathy.
Dhandapany PS, Razzaque MA, Muthusami U, Kunnoth S, Edwards JJ, Mulero-Navarro S, Riess I, Pardo S, Sheng J, Rani DS, Rani B, Govindaraj P, Flex E, Yokota T, Furutani M, Nishizawa T, Nakanishi T, Robbins J, Limongelli G, Hajjar RJ, Lebeche D, Bahl A, Khullar M, Rathinavel A, Sadler KC, Tartaglia M, Matsuoka R, Thangaraj K, Gelb BD. Dhandapany PS, et al. Among authors: govindaraj p. Nat Genet. 2014 Jun;46(6):635-639. doi: 10.1038/ng.2963. Epub 2014 Apr 28. Nat Genet. 2014. PMID: 24777450 Free PMC article.
65 results