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For: Papandreou A, Danti FR, Spaull R, Leuzzi V, Mctague A, Kurian MA. The expanding spectrum of movement disorders in genetic epilepsies. Dev Med Child Neurol 2020;62:178-91. [PMID: 31784983 DOI: 10.1111/dmcn.14407] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Dommel S, Hoffmann A, Berger C, Kern M, Klöting N, Kannt A, Blüher M. Effects of Whole-Body Adenylyl Cyclase 5 (Adcy5) Deficiency on Systemic Insulin Sensitivity and Adipose Tissue. Int J Mol Sci 2021;22:4353. [PMID: 33919448 DOI: 10.3390/ijms22094353] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Wang J, Xiao L, Wang J, Ding Z, Ni J, Long X. Mosaic ring chromosome 18 in a Chinese child with epilepsy: a case report and review of the literature. Neurol Sci 2021. [PMID: 33829328 DOI: 10.1007/s10072-021-05143-z] [Reference Citation Analysis]
3 Gannamani R, van der Veen S, van Egmond M, de Koning TJ, Tijssen MAJ. Challenges in Clinicogenetic Correlations: One Phenotype - Many Genes. Mov Disord Clin Pract 2021;8:311-21. [PMID: 33816658 DOI: 10.1002/mdc3.13163] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
4 Dzinovic I, Škorvánek M, Necpál J, Boesch S, Švantnerová J, Wagner M, Havránková P, Pavelekova P, Haň V, Janzarik WG, Berweck S, Diebold I, Kuster A, Jech R, Winkelmann J, Zech M. Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series. Parkinsonism Relat Disord 2021;90:73-8. [PMID: 34399161 DOI: 10.1016/j.parkreldis.2021.08.007] [Reference Citation Analysis]
5 Mastrangelo M, Galosi S, Cesario S, Renzi A, Campea L, Leuzzi V. Presenting Patterns of Genetically Determined Developmental Encephalopathies With Epilepsy and Movement Disorders: A Single Tertiary Center Retrospective Cohort Study. Front Neurol 2022;13:855134. [DOI: 10.3389/fneur.2022.855134] [Reference Citation Analysis]
6 Ahn H, Ko T. The Genetic Relationship between Paroxysmal Movement Disorders and Epilepsy. Ann Child Neurol 2020;28:76-87. [DOI: 10.26815/acn.2020.00073] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Steel D, Kurian MA. Recent genetic advances in early-onset dystonia. Curr Opin Neurol 2020;33:500-7. [PMID: 32657892 DOI: 10.1097/WCO.0000000000000831] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
8 Spagnoli C, Fusco C, Percesepe A, Leuzzi V, Pisani F. Genetic Neonatal-Onset Epilepsies and Developmental/Epileptic Encephalopathies with Movement Disorders: A Systematic Review. Int J Mol Sci 2021;22:4202. [PMID: 33919646 DOI: 10.3390/ijms22084202] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Liu Z, Naler LB, Zhu Y, Deng C, Zhang Q, Zhu B, Zhou Z, Sarma M, Murray A, Xie H, Lu C. nMOWChIP-seq: low-input genome-wide mapping of non-histone targets. NAR Genom Bioinform 2022;4:lqac030. [PMID: 35402909 DOI: 10.1093/nargab/lqac030] [Reference Citation Analysis]
10 Briere LC, Walker MA, High FA, Cooper C, Rogers CA, Callahan CJ, Ishimura R, Ichimura Y, Caruso PA, Sharma N, Brokamp E, Koziura ME, Mohammad SS, Dale RC, Riley LG, Phillips JA, Komatsu M, Sweetser DA; Undiagnosed Diseases Network. A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy. Cold Spring Harb Mol Case Stud 2021;7:a005827. [PMID: 33811063 DOI: 10.1101/mcs.a005827] [Reference Citation Analysis]
11 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]
12 Lange LM, Gonzalez-Latapi P, Rajalingam R, Tijssen MAJ, Ebrahimi-Fakhari D, Gabbert C, Ganos C, Ghosh R, Kumar KR, Lang AE, Rossi M, van der Veen S, van de Warrenburg B, Warner T, Lohmann K, Klein C, Marras C; on behalf of the Task Force on Genetic Nomenclature in Movement Disorders. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update. Mov Disord 2022. [PMID: 35481685 DOI: 10.1002/mds.28982] [Reference Citation Analysis]
13 Kim M, Yum M, Seo GH, Ko T, Lee BH. Phenotypic and Genetic Complexity in Pediatric Movement Disorders. Front Genet 2022;13:829558. [DOI: 10.3389/fgene.2022.829558] [Reference Citation Analysis]
14 Harvey S, King MD, Gorman KM. Paroxysmal Movement Disorders. Front Neurol 2021;12:659064. [PMID: 34177764 DOI: 10.3389/fneur.2021.659064] [Reference Citation Analysis]
15 Morrison-Levy N, Borlot F, Jain P, Whitney R. Early-Onset Developmental and Epileptic Encephalopathies of Infancy: An Overview of the Genetic Basis and Clinical Features. Pediatr Neurol 2021;116:85-94. [PMID: 33515866 DOI: 10.1016/j.pediatrneurol.2020.12.001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]