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5. 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]
6. CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2. Robbins MS; Lipton RB; Laureta EC; Grosberg BM Headache; 2009 Jul; 49(7):1042-6. PubMed ID: 19486177 [TBL] [Abstract][Full Text] [Related]
7. A family of episodic ataxia type 2: no evidence of genetic linkage to the CACNA1A gene. Hirose H; Arayama T; Takita J; Igarashi T; Hayashi Y; Nagao Y Int J Mol Med; 2003 Feb; 11(2):187-9. PubMed ID: 12525875 [TBL] [Abstract][Full Text] [Related]
8. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop. Cricchi F; Di Lorenzo C; Grieco GS; Rengo C; Cardinale A; Racaniello M; Santorelli FM; Nappi G; Pierelli F; Casali C J Neurol Sci; 2007 Mar; 254(1-2):69-71. PubMed ID: 17292920 [TBL] [Abstract][Full Text] [Related]
9. [Optokynetic and ocular dysmetria tests in the diagnosis of atypical internuclear ophthalmoplegia (author's transl)]. Mutani R; Agnetti V; Fassio F; Monaco F Riv Patol Nerv Ment; 1978; 99(3):135-40. PubMed ID: 752905 [TBL] [Abstract][Full Text] [Related]
10. Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation. Blumkin L; Michelson M; Leshinsky-Silver E; Kivity S; Lev D; Lerman-Sagie T J Child Neurol; 2010 Jul; 25(7):892-7. PubMed ID: 20097664 [TBL] [Abstract][Full Text] [Related]
11. Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene. Cuenca-León E; Banchs I; Serra SA; Latorre P; Fernàndez-Castillo N; Corominas R; Valverde MA; Volpini V; Fernández-Fernández JM; Macaya A; Cormand B J Neurol Sci; 2009 May; 280(1-2):10-4. PubMed ID: 19232643 [TBL] [Abstract][Full Text] [Related]
13. A model-based study of internuclear ophthalmoparesis and ocular-motor fatigue in multiple sclerosis. Jacobs JB; Chisari C; Skelly MM; Walker MF; Serra A Prog Brain Res; 2019; 249():329-344. PubMed ID: 31325992 [TBL] [Abstract][Full Text] [Related]
14. Otolith function in cerebellar ataxia due to mutations in the calcium channel gene CACNA1A. Wiest G; Tian JR; Baloh RW; Crane BT; Demer JL Brain; 2001 Dec; 124(Pt 12):2407-16. PubMed ID: 11701595 [TBL] [Abstract][Full Text] [Related]
15. A new clinical technique for demonstrating changes in eye acceleration during horizontal saccades in patients with partial internuclear ophthalmoplegias. Brown P J Neuroophthalmol; 1998 Mar; 18(1):36-9. PubMed ID: 9532538 [TBL] [Abstract][Full Text] [Related]
16. Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation. Zafeiriou DI; Lehmann-Horn F; Vargiami E; Teflioudi E; Ververi A; Jurkat-Rott K Eur J Paediatr Neurol; 2009 Mar; 13(2):191-3. PubMed ID: 18602318 [TBL] [Abstract][Full Text] [Related]
17. [Clinically detectable oculomotor disorders in multiple sclerosis. Results of studies on 100 patients]. Müri RM; Meienberg O Nervenarzt; 1987 Mar; 58(3):171-4. PubMed ID: 3587451 [TBL] [Abstract][Full Text] [Related]
18. Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study. Harno H; Heikkinen S; Kaunisto MA; Kallela M; Häkkinen AM; Wessman M; Färkkilä M; Lundbom N Neurology; 2005 Feb; 64(3):542-4. PubMed ID: 15699392 [TBL] [Abstract][Full Text] [Related]
19. 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]