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For: Paulhus K, Ammerman L, Glasscock E. Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity. Int J Mol Sci 2020;21:E2802. [PMID: 32316562 DOI: 10.3390/ijms21082802] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Kegele J, Krüger J, Koko M, Lange L, Marco Hernandez AV, Martinez F, Münchau A, Lerche H, Lauxmann S. Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related Disorders. Front Neurol 2021;12:701351. [PMID: 34305802 DOI: 10.3389/fneur.2021.701351] [Reference Citation Analysis]
2 Lee GB, Kim GY, Jeong IH, Kim N, Kim JW. A Novel KCNA1 Mutation in an Episodic Ataxia Type 1 Patient with Asterixis and Falls. J Clin Neurol 2021;17:333-5. [PMID: 33835760 DOI: 10.3988/jcn.2021.17.2.333] [Reference Citation Analysis]
3 Claverie-Martin F, Perdomo-Ramirez A, Garcia-Nieto V. Hereditary kidney diseases associated with hypomagnesemia. Kidney Res Clin Pract 2021. [PMID: 34784661 DOI: 10.23876/j.krcp.21.112] [Reference Citation Analysis]
4 Dinoi G, Morin M, Conte E, Mor Shaked H, Coppola MA, D’adamo MC, Elpeleg O, Liantonio A, Hartmann I, De Luca A, Blunck R, Russo A, Imbrici P. Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia. IJMS 2022;23:8079. [DOI: 10.3390/ijms23158079] [Reference Citation Analysis]
5 Thouta S, Zhang Y, Garcia E, Snutch TP. Kv1.1 channels mediate network excitability and feed-forward inhibition in local amygdala circuits. Sci Rep 2021;11:15180. [PMID: 34312446 DOI: 10.1038/s41598-021-94633-3] [Reference Citation Analysis]
6 Bhattacharjee S, Deenadayalu A, Paramanandam V. Interictal Headache, Pseudodystonia, and Persistent Ataxia in Episodic Ataxia Type 1 Due to a Novel KCNA1 Gene Mutation. Movement Disord Clin Pract 2022;9:272-4. [DOI: 10.1002/mdc3.13381] [Reference Citation Analysis]
7 Trosclair K, Si M, Watts M, Gautier NM, Voigt N, Traylor J, Bitay M, Baczko I, Dobrev D, Hamilton KA, Bhuiyan MS, Dominic P, Glasscock E. Kv1.1 potassium channel subunit deficiency alters ventricular arrhythmia susceptibility, contractility, and repolarization. Physiol Rep 2021;9:e14702. [PMID: 33427415 DOI: 10.14814/phy2.14702] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Simkin D, Marshall KA, Vanoye CG, Desai RR, Bustos BI, Piyevsky BN, Ortega JA, Forrest M, Robertson GL, Penzes P, Laux LC, Lubbe SJ, Millichap JJ, George AL Jr, Kiskinis E. Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy. Elife 2021;10:e64434. [PMID: 33544076 DOI: 10.7554/eLife.64434] [Reference Citation Analysis]
9 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]
10 Miceli F, Guerrini R, Nappi M, Soldovieri MV, Cellini E, Gurnett CA, Parmeggiani L, Mei D, Taglialatela M. Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants. Epilepsia 2021. [PMID: 34778950 DOI: 10.1111/epi.17118] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Ma L, Han L, Niu M, Chen L, Yu Y, Feng T. Screening of the TMEM151A Gene in Patients With Paroxysmal Kinesigenic Dyskinesia and Other Movement Disorders. Front Neurol 2022;13:865690. [DOI: 10.3389/fneur.2022.865690] [Reference Citation Analysis]
12 Amadori E, Pellino G, Bansal L, Mazzone S, Møller RS, Rubboli G, Striano P, Russo A. Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy. European Journal of Medical Genetics 2022. [DOI: 10.1016/j.ejmg.2022.104450] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Indumathy J, Pruitt A, Gautier NM, Crane K, Glasscock E. Kv1.1 deficiency alters repetitive and social behaviors in mice and rescues autistic-like behaviors due to Scn2a haploinsufficiency. Brain Behav 2021;11:e02041. [PMID: 33484493 DOI: 10.1002/brb3.2041] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
14 Maggi L, Bonanno S, Altamura C, Desaphy JF. Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy. Cells 2021;10:1521. [PMID: 34208776 DOI: 10.3390/cells10061521] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
15 Deodhar M, Matthews SA, Thomas B, Adamian L, Mattes S, Wells T, Zieba B, Simeone KA, Simeone TA. Pharmacoresponsiveness of spontaneous recurrent seizures and the comorbid sleep disorder of epileptic Kcna1-null mice. Eur J Pharmacol 2021;913:174656. [PMID: 34838797 DOI: 10.1016/j.ejphar.2021.174656] [Reference Citation Analysis]
16 Sahly AN, Shevell M, Sadleir LG, Myers KA. SUDEP risk and autonomic dysfunction in genetic epilepsies. Auton Neurosci 2021;237:102907. [PMID: 34773737 DOI: 10.1016/j.autneu.2021.102907] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
17 Döring JH, Schröter J, Jüngling J, Biskup S, Klotz KA, Bast T, Dietel T, Korenke GC, Christoph S, Brennenstuhl H, Rubboli G, Møller RS, Lesca G, Chaix Y, Kölker S, Hoffmann GF, Lemke JR, Syrbe S. Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders. Int J Mol Sci 2021;22:2824. [PMID: 33802230 DOI: 10.3390/ijms22062824] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
18 Imbrici P, Accogli A, Blunck R, Altamura C, Iacomino M, D'adamo MC, Allegri A, Pedemonte M, Brolatti N, Vari S, Cataldi M, Capra V, Gustincich S, Zara F, Desaphy JF, Fiorillo C. Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel. Biomedicines 2021;9:75. [PMID: 33466780 DOI: 10.3390/biomedicines9010075] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 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]
20 Benarroch E. What Is the Role of Potassium Channels in Ataxia? Neurology 2021;97:938-41. [PMID: 34782409 DOI: 10.1212/WNL.0000000000012870] [Reference Citation Analysis]
21 Xu C, Zhang Y, Gozal D, Carney P. Channelopathy of Dravet Syndrome and Potential Neuroprotective Effects of Cannabidiol. J Cent Nerv Syst Dis 2021;13:11795735211048045. [PMID: 34992485 DOI: 10.1177/11795735211048045] [Reference Citation Analysis]
22 Tseng MH, Konrad M, Ding JJ, Lin SH. Clinical and Genetic Approach to Renal Hypomagnesemia. Biomed J 2021:S2319-4170(21)00150-5. [PMID: 34767995 DOI: 10.1016/j.bj.2021.11.002] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
23 Danti FR, Invernizzi F, Moroni I, Garavaglia B, Nardocci N, Zorzi G. Pediatric Paroxysmal Exercise-Induced Neurological Symptoms: Clinical Spectrum and Diagnostic Algorithm. Front Neurol 2021;12:658178. [PMID: 34140924 DOI: 10.3389/fneur.2021.658178] [Reference Citation Analysis]
24 Choi HW. Fasciculations in Children. Pediatr Neurol 2021;125:40-7. [PMID: 34628142 DOI: 10.1016/j.pediatrneurol.2021.08.008] [Reference Citation Analysis]