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Novel SCN3A variants associated with focal epilepsy in children.
Vanoye CG, Gurnett CA, Holland KD, George AL Jr, Kearney JA. Vanoye CG, et al. Among authors: holland kd. Neurobiol Dis. 2014 Feb;62:313-22. doi: 10.1016/j.nbd.2013.10.015. Epub 2013 Oct 21. Neurobiol Dis. 2014. PMID: 24157691 Free PMC article.
Genetic Testing in Epilepsy.
Ritter DM, Holland K. Ritter DM, et al. Semin Neurol. 2020 Dec;40(6):730-738. doi: 10.1055/s-0040-1719070. Epub 2020 Nov 11. Semin Neurol. 2020. PMID: 33176374 Review.
When should clinicians order genetic testing for Dravet syndrome?
Fountain-Capal JK, Holland KD, Gilbert DL, Hallinan BE. Fountain-Capal JK, et al. Among authors: holland kd. Pediatr Neurol. 2011 Nov;45(5):319-23. doi: 10.1016/j.pediatrneurol.2011.08.001. Pediatr Neurol. 2011. PMID: 22000312 Free PMC article.
In Silico Predictions of KCNQ Variant Pathogenicity in Epilepsy.
Ritter DM, Horn PS, Holland KD. Ritter DM, et al. Among authors: holland kd. Pediatr Neurol. 2021 May;118:48-54. doi: 10.1016/j.pediatrneurol.2021.01.006. Epub 2021 Jan 27. Pediatr Neurol. 2021. PMID: 33784504 Free PMC article.
113 results