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

Year Number of Results
1982 2
1985 2
1986 4
1987 7
1988 5
1989 7
1990 3
1991 2
1992 2
1993 2
1994 7
1995 12
1996 4
1997 5
1998 6
1999 8
2000 1
2001 6
2002 4
2003 6
2004 10
2005 8
2006 10
2007 15
2008 19
2009 10
2010 18
2011 8
2012 15
2013 23
2014 16
2015 22
2016 26
2017 23
2018 13
2019 6
2020 10
2021 15
2022 11
2023 0
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341 results
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Page 1
Charcot Marie Tooth.
Nagappa M, Sharma S, Taly AB. Nagappa M, et al. Among authors: taly ab. 2022 Aug 22. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. 2022 Aug 22. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. PMID: 32965834 Free Books & Documents.
Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.
Singh N, Kallollimath P, Shah MH, Kapoor S, Bhat VK, Viswanathan LG, Nagappa M, Bindu PS, Taly AB, Sinha S, Kumar A. Singh N, et al. Among authors: taly ab. PLoS One. 2019 May 6;14(5):e0215779. doi: 10.1371/journal.pone.0215779. eCollection 2019. PLoS One. 2019. PMID: 31059521 Free PMC article.
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
Chakrabarty S, Govindaraj P, Sankaran BP, Nagappa M, Kabekkodu SP, Jayaram P, Mallya S, Deepha S, Ponmalar JNJ, Arivinda HR, Meena AK, Jha RK, Sinha S, Gayathri N, Taly AB, Thangaraj K, Satyamoorthy K. Chakrabarty S, et al. Among authors: taly ab. J Neurol. 2021 Jun;268(6):2192-2207. doi: 10.1007/s00415-020-10390-9. Epub 2021 Jan 23. J Neurol. 2021. PMID: 33484326 Free PMC article.
Isolated Sulfite Oxidase Deficiency.
Bindu PS, Nagappa M, Bharath RD, Taly AB. Bindu PS, et al. Among authors: taly ab. 2017 Sep 21. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2017 Sep 21. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 28933809 Free Books & Documents. Review.
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: taly ab. 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: taly ab. Can J Neurol Sci. 2022 Sep;49(5):708-712. doi: 10.1017/cjn.2021.202. Epub 2021 Sep 2. Can J Neurol Sci. 2022. PMID: 34663487
Vogt-Koyanagi-Harada Syndrome - A Neurologist's Perspective.
Shivaram S, Nagappa M, Seshagiri DV, Shanthakumar JS, Panda SS, Anadure R, Nandeesh BN, Chickabasaviah YT, Bharath RD, Vijayan J, Kashyap B, Sinha S, Taly AB. Shivaram S, et al. Among authors: taly ab. Ann Indian Acad Neurol. 2021 May-Jun;24(3):405-409. doi: 10.4103/aian.AIAN_405_20. Epub 2020 Jul 31. Ann Indian Acad Neurol. 2021. PMID: 34447006 Free PMC article.
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. Among authors: taly ab. Neurology. 2020 Mar 24;94(12):e1336-e1339. doi: 10.1212/WNL.0000000000009144. Epub 2020 Feb 28. Neurology. 2020. PMID: 32111695 No abstract available.
Giant axonal neuropathy.
Vijaykumar K, Bindu PS, Taly AB, Mahadevan A, Bharath RD, Gayathri N, Nagappa M, Sinha S. Vijaykumar K, et al. Among authors: taly ab. J Child Neurol. 2015 Jun;30(7):912-5. doi: 10.1177/0883073814547721. Epub 2014 Sep 11. J Child Neurol. 2015. PMID: 25213662
341 results