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Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice.
JAMA Neurol. 2022 Dec 1;79(12):1267-1276. doi: 10.1001/jamaneurol.2022.3651.
JAMA Neurol. 2022.
PMID: 36315135
Free PMC article.
Atypical imaging evolution of sturge-weber syndrome without facial nevus.
Luke RR, Malik SI, Hernandez AW, Donahue DJ, Perry MS.
Luke RR, et al.
Pediatr Neurol. 2013 Feb;48(2):143-5. doi: 10.1016/j.pediatrneurol.2012.10.002.
Pediatr Neurol. 2013.
PMID: 23337009
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Response.
Malik SI, Hernandez A, Donahue D, Perry MS, Luke RR.
Malik SI, et al. Among authors: luke rr.
Pediatr Neurol. 2013 Jul;49(1):e1-2. doi: 10.1016/j.pediatrneurol.2013.03.001.
Pediatr Neurol. 2013.
PMID: 23827434
No abstract available.
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Expanding the genotype-phenotype correlation of childhood sensory polyneuropathy of genetic origin.
Chakravorty S, Logan R, Elson MJ, Luke RR, Verma S.
Chakravorty S, et al. Among authors: luke rr.
Sci Rep. 2020 Sep 30;10(1):16184. doi: 10.1038/s41598-020-73219-5.
Sci Rep. 2020.
PMID: 32999401
Free PMC article.
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