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Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy.
Glauser TA, Holland K, O'Brien VP, Keddache M, Martin LJ, Clark PO, Cnaan A, Dlugos D, Hirtz DG, Shinnar S, Grabowski G; Childhood Absence Epilepsy Study Group. Glauser TA, et al. Among authors: keddache m. Ann Neurol. 2017 Mar;81(3):444-453. doi: 10.1002/ana.24886. Ann Neurol. 2017. PMID: 28165634 Free PMC article. Clinical Trial.
NF1 patient missense variants predict a role for ATM in modifying neurofibroma initiation.
Yu Y, Choi K, Wu J, Andreassen PR, Dexheimer PJ, Keddache M, Brems H, Spinner RJ, Cancelas JA, Martin LJ, Wallace MR, Legius E, Vogel KS, Ratner N. Yu Y, et al. Among authors: keddache m. Acta Neuropathol. 2020 Jan;139(1):157-174. doi: 10.1007/s00401-019-02086-w. Epub 2019 Oct 29. Acta Neuropathol. 2020. PMID: 31664505 Free PMC article.
Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model.
Dasgupta N, Xu YH, Li R, Peng Y, Pandey MK, Tinch SL, Liou B, Inskeep V, Zhang W, Setchell KD, Keddache M, Grabowski GA, Sun Y. Dasgupta N, et al. Among authors: keddache m. Hum Mol Genet. 2015 Dec 15;24(24):7031-48. doi: 10.1093/hmg/ddv404. Epub 2015 Sep 29. Hum Mol Genet. 2015. PMID: 26420838 Free PMC article.
50 results