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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
Post-Treatment Movement Disorder in a Child with Late-onset Cobalamin Deficiency.
Fadilah A, Baxter PS, Sarrigiannis PG, Sengupta S, Sharrard MJ, Mordekar SR. Fadilah A, et al. Among authors: mordekar sr. Mov Disord Clin Pract. 2021 Dec 27;9(2):245-248. doi: 10.1002/mdc3.13387. eCollection 2022 Feb. Mov Disord Clin Pract. 2021. PMID: 35146063 Free PMC article. No abstract available.
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.
Stroke in a child with neurofibromatosis type 2.
Ng J, Mordekar SR, Connolly DJ, Baxter P. Ng J, et al. Eur J Paediatr Neurol. 2009 Jan;13(1):77-9. doi: 10.1016/j.ejpn.2008.02.007. Epub 2008 Apr 11. Eur J Paediatr Neurol. 2009. PMID: 18406647
53 results