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

Year Number of Results
1993 2
2005 1
2006 1
2007 6
2008 2
2009 3
2010 7
2011 3
2012 9
2013 16
2014 16
2015 19
2016 14
2017 12
2018 11
2019 6
2020 7
2021 3
2022 5
2023 1
2024 1
2025 0

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120 results

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Page 1
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: bindu ps. PLoS One. 2019 May 6;14(5):e0215779. doi: 10.1371/journal.pone.0215779. eCollection 2019. PLoS One. 2019. PMID: 31059521 Free PMC article.
Huppke-Brendel Syndrome.
Bindu PS, Chiplunkar S, Vandana VP, Nagappa M, Govindaraj P, Taly A. Bindu PS, et al. 2019 Jun 13. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2019 Jun 13. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 31194315 Free Books & Documents. Review.
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GMH, Karminejad A, Kara M, Kara B, Bozorgmehri B, Ben-Omran T, Mojahedi F, El Din Mahmoud IG, Bouslam N, Bouhouche A, Benomar A, Hanein S, Raymond L, Forlani S, Mascaro M, Selim L, Shehata N, Al-Allawi N, Bindu PS, Azam M, Gunel M, Caglayan A, Bilguvar K, Tolun A, Issa MY, Schroth J, Spencer EG, Rosti RO, Akizu N, Vaux KK, Johansen A, Koh AA, Megahed H, Durr A, Brice A, Stevanin G, Gabriel SB, Ideker T, Gleeson JG. Novarino G, et al. Among authors: bindu ps. Science. 2014 Jan 31;343(6170):506-511. doi: 10.1126/science.1247363. Science. 2014. PMID: 24482476 Free PMC article.
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: bindu ps. J Child Neurol. 2015 Jun;30(7):912-5. doi: 10.1177/0883073814547721. Epub 2014 Sep 11. J Child Neurol. 2015. PMID: 25213662
Isolated Sulfite Oxidase Deficiency.
Bindu PS, Nagappa M, Bharath RD, Taly AB. Bindu PS, et al. 2017 Sep 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2017 Sep 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 28933809 Free Books & Documents. Review.
Child Neurology: Sjögren-Larsson syndrome.
Nagappa M, Bindu PS, Chiplunkar S, Gupta N, Sinha S, Mathuranath PS, Bharath RD, Taly AB. Nagappa M, et al. Among authors: bindu ps. Neurology. 2017 Jan 3;88(1):e1-e4. doi: 10.1212/WNL.0000000000003456. Neurology. 2017. PMID: 28025403 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: bindu ps. 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
Therapeutic strategies for mitochondrial disorders.
Finsterer J, Bindu PS. Finsterer J, et al. Among authors: bindu ps. Pediatr Neurol. 2015 Mar;52(3):302-13. doi: 10.1016/j.pediatrneurol.2014.06.023. Epub 2014 Nov 15. Pediatr Neurol. 2015. PMID: 25701186 Review.
120 results