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For: Lee EH. Epilepsy syndromes during the first year of life and the usefulness of an epilepsy gene panel. Korean J Pediatr 2018;61:101-7. [PMID: 29713355 DOI: 10.3345/kjp.2018.61.4.101] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Rapaccini V, Esposito S, Strinati F, Allegretti M, Manfroi E, Miconi F, Pitzianti M, Prontera P, Principi N, Pasini A. A Child with a c.6923_6928dup (p.Arg2308_Met2309dup) SPTAN1 Mutation Associated with a Severe Early Infantile Epileptic Encephalopathy. Int J Mol Sci 2018;19:E1976. [PMID: 29986434 DOI: 10.3390/ijms19071976] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
2 Deng Y, Xu J, Yao C, Wang L, Dong X, Zhao C. Characteristics of infantile convulsions and choreoathetosis syndrome caused by PRRT2 mutation. Pediatric Investigation. [DOI: 10.1002/ped4.12308] [Reference Citation Analysis]
3 Jaxybayeva A, Nauryzbayeva A, Khamzina A, Takhanova M, Abilhadirova A, Rybalko A, Jamanbekova K. Genomic Investigation of Infantile and Childhood Epileptic Encephalopathies in Kazakhstan: An Urgent Priority. Front Neurol 2021;12:639317. [PMID: 34177756 DOI: 10.3389/fneur.2021.639317] [Reference Citation Analysis]
4 van Roest A, Van de Vel A, Lederer D, Ceulemans B. The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures. Eur J Paediatr Neurol 2020;24:148-53. [PMID: 31901402 DOI: 10.1016/j.ejpn.2019.12.003] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Marco Hernández AV, Caro A, Montoya Filardi A, Tomás Vila M, Monfort S, Beseler Soto B, Nieto-Barceló JJ, Martínez F. Extending the clinical phenotype of SPTAN1: From DEE5 to migraine, epilepsy, and subependymal heterotopias without intellectual disability. Am J Med Genet A 2021. [PMID: 34590414 DOI: 10.1002/ajmg.a.62507] [Reference Citation Analysis]
6 Bayat A, Bayat M, Rubboli G, Møller RS. Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy. Genes (Basel) 2021;12:1051. [PMID: 34356067 DOI: 10.3390/genes12071051] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
7 Yu X, Yang L, Li J, Li W, Li D, Wang R, Wu K, Chen W, Zhang Y, Qiu Z, Zhou W. De Novo and Inherited SETD1A Variants in Early-onset Epilepsy. Neurosci Bull 2019;35:1045-57. [PMID: 31197650 DOI: 10.1007/s12264-019-00400-w] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
8 Balasundaram P, Fijas M, Nafday S. A Rare Case of Lethal Neonatal Rigidity and Multi-Focal Seizure Syndrome. Cureus 2021;13:e13600. [PMID: 33816000 DOI: 10.7759/cureus.13600] [Reference Citation Analysis]