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Cited by in F6Publishing
For: de Gusmão CM, Garcia L, Mikati MA, Su S, Silveira-Moriyama L. Paroxysmal Genetic Movement Disorders and Epilepsy. Front Neurol 2021;12:648031. [PMID: 33833732 DOI: 10.3389/fneur.2021.648031] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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1 Lauxmann S, Sonnenberg L, Koch NA, Bosselmann C, Winter N, Schwarz N, Wuttke TV, Hedrich UBS, Liu Y, Lerche H, Benda J, Kegele J. Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature. Front Neurol 2021;12:703970. [PMID: 34566847 DOI: 10.3389/fneur.2021.703970] [Reference Citation Analysis]
2 Tian M, Chen J, Li J, Pan H, Lei W, Shu X. Damaging novel mutations in PIGN cause developmental epileptic-dyskinetic encephalopathy: a case report. BMC Pediatr 2022;22:222. [PMID: 35468813 DOI: 10.1186/s12887-022-03246-w] [Reference Citation Analysis]
3 De Rosa A, Balint B, Kumar KR. Editorial: Genetics of Paroxysmal Movement Disorders. Front Neurol 2021;12:752000. [PMID: 34650515 DOI: 10.3389/fneur.2021.752000] [Reference Citation Analysis]
4 Geng J, Zheng Y, Li Q, Hou Q, Wang X, Jiang Y. Case Report: A Case of Concomitant Paroxysmal Kinesigenic Dyskinesia and Epilepsy: Can We Treat Two Birds With One Stone? Front Neurol 2022;13:826897. [DOI: 10.3389/fneur.2022.826897] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]