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Severity Assessment in CDKL5 Deficiency Disorder.
Demarest S, Pestana-Knight EM, Olson HE, Downs J, Marsh ED, Kaufmann WE, Partridge CA, Leonard H, Gwadry-Sridhar F, Frame KE, Cross JH, Chin RFM, Parikh S, Panzer A, Weisenberg J, Utley K, Jaksha A, Amin S, Khwaja O, Devinsky O, Neul JL, Percy AK, Benke TA. Demarest S, et al. Among authors: parikh s. Pediatr Neurol. 2019 Aug;97:38-42. doi: 10.1016/j.pediatrneurol.2019.03.017. Epub 2019 Mar 27. Pediatr Neurol. 2019. PMID: 31147226 Free PMC article. Review.
Neurologic disorders due to mitochondrial DNA mutations.
Debrosse S, Parikh S. Debrosse S, et al. Among authors: parikh s. Semin Pediatr Neurol. 2012 Dec;19(4):194-202. doi: 10.1016/j.spen.2012.09.006. Semin Pediatr Neurol. 2012. PMID: 23245552 Review.
Treatment of mitochondrial disorders.
Avula S, Parikh S, Demarest S, Kurz J, Gropman A. Avula S, et al. Among authors: parikh s. Curr Treat Options Neurol. 2014 Jun;16(6):292. doi: 10.1007/s11940-014-0292-7. Curr Treat Options Neurol. 2014. PMID: 24700433 Free PMC article.
2,068 results