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

Year Number of Results
1994 1
2004 2
2005 2
2006 2
2007 4
2008 3
2009 6
2010 2
2011 8
2012 7
2013 4
2014 3
2015 3
2016 2
2017 4
2018 3
2019 2
2021 4
2022 4
2023 1
2024 1

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52 results

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Page 1
The Phenotypic Continuum of ATP1A3-Related Disorders.
Vezyroglou A, Akilapa R, Barwick K, Koene S, Brownstein CA, Holder-Espinasse M, Fry AE, Németh AH, Tofaris GK, Hay E, Hughes I, Mansour S, Mordekar SR, Splitt M, Turnpenny PD, Demetriou D, Koopmann TT, Ruivenkamp CAL, Agrawal PB, Carr L, Clowes V, Ghali N, Holder SE, Radley J, Male A, Sisodiya SM, Kurian MA, Cross JH, Balasubramanian M. Vezyroglou A, et al. Among authors: mordekar sr. Neurology. 2022 Oct 4;99(14):e1511-e1526. doi: 10.1212/WNL.0000000000200927. Epub 2022 Jul 18. Neurology. 2022. PMID: 36192182 Free PMC article. Review.
Neonatal hypertonia - a diagnostic challenge.
Hart AR, Sharma R, Rittey CD, Mordekar SR. Hart AR, et al. Among authors: mordekar sr. Dev Med Child Neurol. 2015 Jul;57(7):600-610. doi: 10.1111/dmcn.12658. Epub 2014 Dec 12. Dev Med Child Neurol. 2015. PMID: 25495611 Free article. Review.
The encephalopathic child.
Abeyakoon O, Batty R, Mordekar S, Raghavan A, Sinha S, Griffiths PD, Connolly DJ. Abeyakoon O, et al. Among authors: mordekar s. Neuroradiol J. 2011 Aug 31;24(4):483-502. doi: 10.1177/197140091102400403. Epub 2011 Sep 2. Neuroradiol J. 2011. PMID: 24059705
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome.
Masnada S, Sarret C, Antonello CE, Fadilah A, Krude H, Mura E, Mordekar S, Nicita F, Olivotto S, Orcesi S, Porta F, Remerand G, Siri B, Wilpert NM, Amir-Yazdani P, Bertini E, Schuelke M, Bernard G, Boespflug-Tanguy O, Tonduti D. Masnada S, et al. Among authors: mordekar s. Mol Genet Metab. 2022 Jan;135(1):109-113. doi: 10.1016/j.ymgme.2021.12.003. Epub 2021 Dec 16. Mol Genet Metab. 2022. PMID: 34969638
Fifteen minute consultation: tics and Tourette syndrome.
Ong MT, Mordekar SR, Seal A. Ong MT, et al. Among authors: mordekar sr. Arch Dis Child Educ Pract Ed. 2016 Apr;101(2):87-94. doi: 10.1136/archdischild-2015-309138. Epub 2015 Sep 22. Arch Dis Child Educ Pract Ed. 2016. PMID: 26396225 Review.
Novel <i>DNM1L</i> variants impair mitochondrial dynamics through divergent mechanisms.
Nolden KA, Egner JM, Collier JJ, Russell OM, Alston CL, Harwig MC, Widlansky ME, Sasorith S, Barbosa IA, Douglas AG, Baptista J, Walker M, Donnelly DE, Morris AA, Tan HJ, Kurian MA, Gorman K, Mordekar S, Deshpande C, Samanta R, McFarland R, Hill RB, Taylor RW, Oláhová M. Nolden KA, et al. Among authors: mordekar s. Life Sci Alliance. 2022 Aug 1;5(12):e202101284. doi: 10.26508/lsa.202101284. Life Sci Alliance. 2022. PMID: 35914810 Free PMC article.
Nonketotic hyperglycinemia case series.
Iqbal M, Prasad M, Mordekar SR. Iqbal M, et al. Among authors: mordekar sr. J Pediatr Neurosci. 2015 Oct-Dec;10(4):355-8. doi: 10.4103/1817-1745.174445. J Pediatr Neurosci. 2015. PMID: 26962342 Free PMC article.
52 results