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2. Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. Reinson K; Õiglane-Shlik E; Talvik I; Vaher U; Õunapuu A; Ennok M; Teek R; Pajusalu S; Murumets Ü; Tomberg T; Puusepp S; Piirsoo A; Reimand T; Õunap K Am J Med Genet A; 2016 Aug; 170(8):2173-6. PubMed ID: 27250579 [TBL] [Abstract][Full Text] [Related]
3. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. Tonelli A; D'Angelo MG; Salati R; Villa L; Germinasi C; Frattini T; Meola G; Turconi AC; Bresolin N; Bassi MT J Neurol Sci; 2006 Feb; 241(1-2):13-7. PubMed ID: 16325861 [TBL] [Abstract][Full Text] [Related]
4. Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant. Nardello R; Plicato G; Mangano GD; Gennaro E; Mangano S; Brighina F; Raieli V; Fontana A BMC Neurol; 2020 Apr; 20(1):155. PubMed ID: 32336275 [TBL] [Abstract][Full Text] [Related]
5. Epilepsy and episodic ataxia type 2: family study and review of the literature. Verriello L; Pauletto G; Nilo A; Lonigro I; Betto E; Valente M; Curcio F; Gigli GL J Neurol; 2021 Nov; 268(11):4296-4302. PubMed ID: 33983550 [TBL] [Abstract][Full Text] [Related]
6. CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics. Wan J; Khanna R; Sandusky M; Papazian DM; Jen JC; Baloh RW Neurology; 2005 Jun; 64(12):2090-7. PubMed ID: 15985579 [TBL] [Abstract][Full Text] [Related]
7. Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation. Pradotto L; Mencarelli M; Bigoni M; Milesi A; Di Blasio A; Mauro A J Neurol Sci; 2016 Dec; 371():81-84. PubMed ID: 27871455 [TBL] [Abstract][Full Text] [Related]
8. Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. Mantuano E; Romano S; Veneziano L; Gellera C; Castellotti B; Caimi S; Testa D; Estienne M; Zorzi G; Bugiani M; Rajabally YA; Barcina MJ; Servidei S; Panico A; Frontali M; Mariotti C J Neurol Sci; 2010 Apr; 291(1-2):30-6. PubMed ID: 20129625 [TBL] [Abstract][Full Text] [Related]
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10. Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia. Stendel C; D'Adamo MC; Wiessner M; Dusl M; Cenciarini M; Belia S; Nematian-Ardestani E; Bauer P; Senderek J; Klopstock T; Pessia M Int J Mol Sci; 2020 May; 21(11):. PubMed ID: 32471306 [TBL] [Abstract][Full Text] [Related]
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13. The neuropsychiatric phenotype in CACNA1A mutations: a retrospective single center study and review of the literature. Indelicato E; Nachbauer W; Karner E; Eigentler A; Wagner M; Unterberger I; Poewe W; Delazer M; Boesch S Eur J Neurol; 2019 Jan; 26(1):66-e7. PubMed ID: 30063100 [TBL] [Abstract][Full Text] [Related]
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16. Link between confusional migraine, hemiplegic migraine and episodic ataxia type 2: hypothesis, family genealogy, gene typing and classification. Cleves C; Parikh S; Rothner AD; Tepper SJ Cephalalgia; 2010 Jun; 30(6):740-3. PubMed ID: 19624685 [TBL] [Abstract][Full Text] [Related]
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19. Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature. Nachbauer W; Nocker M; Karner E; Stankovic I; Unterberger I; Eigentler A; Schneider R; Poewe W; Delazer M; Boesch S J Neurol; 2014 May; 261(5):983-91. PubMed ID: 24658662 [TBL] [Abstract][Full Text] [Related]
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