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Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study.
Kurian MA, Li Y, Zhen J, Meyer E, Hai N, Christen HJ, Hoffmann GF, Jardine P, von Moers A, Mordekar SR, O'Callaghan F, Wassmer E, Wraige E, Dietrich C, Lewis T, Hyland K, Heales S Jr, Sanger T, Gissen P, Assmann BE, Reith ME, Maher ER. Kurian MA, et al. Among authors: mordekar sr. Lancet Neurol. 2011 Jan;10(1):54-62. doi: 10.1016/S1474-4422(10)70269-6. Epub 2010 Nov 25. Lancet Neurol. 2011. PMID: 21112253 Free PMC article.
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.
Kurian MA, Zhen J, Cheng SY, Li Y, Mordekar SR, Jardine P, Morgan NV, Meyer E, Tee L, Pasha S, Wassmer E, Heales SJ, Gissen P, Reith ME, Maher ER. Kurian MA, et al. Among authors: mordekar sr. J Clin Invest. 2009 Jun;119(6):1595-603. doi: 10.1172/JCI39060. Epub 2009 May 26. J Clin Invest. 2009. PMID: 19478460 Free PMC article.
An investigation into the relationship between vigabatrin, movement disorders, and brain magnetic resonance imaging abnormalities in children with infantile spasms.
Fong CY, Osborne JP, Edwards SW, Hemingway C, Hancock E, Johnson AL, Kennedy CR, Kneen R, Likeman M, Lux AL, Mordekar SR, Murugan V, Newton RW, Pike M, Quinn M, Spinty S, Vassallo G, Verity CM, Whitney A, O'Callaghan FJ. Fong CY, et al. Among authors: mordekar sr. Dev Med Child Neurol. 2013 Sep;55(9):862-7. doi: 10.1111/dmcn.12188. Epub 2013 Jun 22. Dev Med Child Neurol. 2013. PMID: 23789722 Free article.
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.
Retention rate of Gabapentin in children with intractable epilepsies at 1 year.
Mills JK, Ruslan NE, Lewis TG, Mughal K, Ali I, Ugar A, Wassmer E, Siddiqua A, Gupta R, Mordekar SR, Sharma R, Sasidharan L, Whitehouse WP. Mills JK, et al. Among authors: mordekar sr. Seizure. 2012 Jan;21(1):28-31. doi: 10.1016/j.seizure.2011.08.013. Epub 2011 Oct 5. Seizure. 2012. PMID: 21982407 Free article.
Novel DNM1L 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. Life Sci Alliance. 2022 Aug 1;5(12):e202101284. doi: 10.26508/lsa.202101284. Life Sci Alliance. 2022. PMID: 35914810 Free PMC article.
Long term outcome in non-multiple sclerosis paediatric acquired demyelinating syndromes.
Wassmer E, Billaud C, Absoud M, Abdel-Mannan O, Benetou C, Cummins C, Forrest K, De Goede C, Eltantawi N, Hickson H, Hussain N, Jardine P, Livingston JH, Mordekar S, Ramdas S, Taylor M, Vijayakumar K, West S, Whitehouse WP, Kneen R, Hemingway C, Lim M, Hacohen Y, Wright S; PUDDLS STUDY GROUP. Wassmer E, et al. Eur J Paediatr Neurol. 2024 Sep;52:52-58. doi: 10.1016/j.ejpn.2024.07.002. Epub 2024 Jul 6. Eur J Paediatr Neurol. 2024. PMID: 39025036 Free article.
52 results