These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
95 related articles for article (PubMed ID: 31017293)
1. [De novo sporadic mutation in the KCND3 gene in a patient with early onset chronic ataxia]. Carrasco-Marina ML; Quijada-Fraile P; Fernandez-Marmiesse A; Gutierrez-Cruz N; Martin-Del Valle F Rev Neurol; 2019 May; 68(9):398-399. PubMed ID: 31017293 [TBL] [Abstract][Full Text] [Related]
2. First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy. Smets K; Duarri A; Deconinck T; Ceulemans B; van de Warrenburg BP; Züchner S; Gonzalez MA; Schüle R; Synofzik M; Van der Aa N; De Jonghe P; Verbeek DS; Baets J BMC Med Genet; 2015 Jul; 16():51. PubMed ID: 26189493 [TBL] [Abstract][Full Text] [Related]
3. Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. Wang J; Wen Y; Zhang Q; Yu S; Chen Y; Wu X; Zhang Y; Bao X Seizure; 2019 Mar; 66():26-30. PubMed ID: 30776697 [TBL] [Abstract][Full Text] [Related]
4. Pollini L; Galosi S; Tolve M; Caputi C; Carducci C; Angeloni A; Leuzzi V Int J Mol Sci; 2020 Aug; 21(16):. PubMed ID: 32823520 [No Abstract] [Full Text] [Related]
7. Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19. Paucar M; Bergendal Å; Gustavsson P; Nordenskjöld M; Laffita-Mesa J; Savitcheva I; Svenningsson P Cerebellum; 2018 Aug; 17(4):465-476. PubMed ID: 29527639 [TBL] [Abstract][Full Text] [Related]
8. Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19. Duarri A; Jezierska J; Fokkens M; Meijer M; Schelhaas HJ; den Dunnen WF; van Dijk F; Verschuuren-Bemelmans C; Hageman G; van de Vlies P; Küsters B; van de Warrenburg BP; Kremer B; Wijmenga C; Sinke RJ; Swertz MA; Kampinga HH; Boddeke E; Verbeek DS Ann Neurol; 2012 Dec; 72(6):870-80. PubMed ID: 23280838 [TBL] [Abstract][Full Text] [Related]
9. Novel Cardiocerebral Channelopathy Associated with a KCND3 V392I Mutation. Nakajima T; Kawabata-Iwakawa R; Kaneko Y; Hamano SI; Sano R; Tamura S; Hasegawa H; Kobari T; Kominato Y; Nishiyama M; Kurabayashi M Int Heart J; 2020 Sep; 61(5):1049-1055. PubMed ID: 32921676 [TBL] [Abstract][Full Text] [Related]
10. KCND3 mutations in Brugada syndrome: the plot thickens. van den Berg MP; Bezzina CR Heart Rhythm; 2011 Jul; 8(7):1033-5. PubMed ID: 21640846 [No Abstract] [Full Text] [Related]
11. Novel SCA19/22-associated KCND3 mutations disrupt human K Hsiao CT; Fu SJ; Liu YT; Lu YH; Zhong CY; Tang CY; Soong BW; Jeng CJ Hum Mutat; 2019 Nov; 40(11):2088-2107. PubMed ID: 31293010 [TBL] [Abstract][Full Text] [Related]
12. VARPRISM: incorporating variant prioritization in tests of de novo mutation association. Hu H; Coon H; Li M; Yandell M; Huff CD Genome Med; 2016 Aug; 8(1):91. PubMed ID: 27562213 [TBL] [Abstract][Full Text] [Related]
13. Kv4.2 autism and epilepsy mutation enhances inactivation of closed channels but impairs access to inactivated state after opening. Lin MA; Cannon SC; Papazian DM Proc Natl Acad Sci U S A; 2018 Apr; 115(15):E3559-E3568. PubMed ID: 29581270 [TBL] [Abstract][Full Text] [Related]
14. Repolarization matters: mutations in the Kv4.3 potassium channel cause SCA19/22. Pulst SM; Otis TS Ann Neurol; 2012 Dec; 72(6):829-31. PubMed ID: 23280833 [No Abstract] [Full Text] [Related]
16. Novel mutation in the KCNJ10 gene in three siblings with seizures, ataxia and no electrolyte abnormalities. Al Dhaibani MA; El-Hattab AW; Holroyd KB; Orthmann-Murphy J; Larson VA; Siddiqui KA; Szolics M; Schiess N J Neurogenet; 2018 Mar; 32(1):1-5. PubMed ID: 29191078 [TBL] [Abstract][Full Text] [Related]
17. De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia. Yue Q; Jen JC; Thwe MM; Nelson SF; Baloh RW Am J Med Genet; 1998 May; 77(4):298-301. PubMed ID: 9600739 [TBL] [Abstract][Full Text] [Related]
19. Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy. Pena SD; Coimbra RL Clin Genet; 2015 Feb; 87(2):e1-3. PubMed ID: 25477152 [TBL] [Abstract][Full Text] [Related]
20. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A. García Segarra N; Gautschi I; Mittaz-Crettol L; Kallay Zetchi C; Al-Qusairi L; Van Bemmelen MX; Maeder P; Bonafé L; Schild L; Roulet-Perez E J Neurol Sci; 2014 Jul; 342(1-2):69-78. PubMed ID: 24836863 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]