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2. Episodic ataxia type 2 characterised by recurrent dizziness/vertigo: a report of four cases. Ling X; Zhao DH; Zhao J; Shen B; Yang X Int J Neurosci; 2019 Feb; 129(2):103-109. PubMed ID: 29883219 [TBL] [Abstract][Full Text] [Related]
3. Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus. Young GF; Leon-Barth CA; Green J Arch Neurol; 1970 Sep; 23(3):201-9. PubMed ID: 5311627 [No Abstract] [Full Text] [Related]
4. Ataxia and oscillopsia in downbeat-nystagmus vertigo syndrome. Büchele W; Brandt T; Degner D Adv Otorhinolaryngol; 1983; 30():291-7. PubMed ID: 12325208 [No Abstract] [Full Text] [Related]
5. A novel CACNA1A mutation associated with episodic ataxia 2 presenting with periodic paralysis. Park D; Kim SH; Lee YJ; Song GJ; Park JS Acta Neurol Belg; 2018 Mar; 118(1):137-139. PubMed ID: 29442233 [No Abstract] [Full Text] [Related]
6. Benign paroxysmal vertigo of childhood: a migraine equivalent. Koehler B Eur J Pediatr; 1980 Aug; 134(2):149-51. PubMed ID: 7439200 [TBL] [Abstract][Full Text] [Related]
8. Familial cerebellar ataxia presenting with down beat nystagmus. Schott GD J Med Genet; 1980 Apr; 17(2):115-8. PubMed ID: 7381864 [TBL] [Abstract][Full Text] [Related]
9. A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p. Kramer PL; Yue Q; Gancher ST; Nutt JG; Baloh R; Smith E; Browne D; Bussey K; Lovrien E; Nelson S Am J Hum Genet; 1995 Jul; 57(1):182-5. PubMed ID: 7611286 [No Abstract] [Full Text] [Related]
10. An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. Steckley JL; Ebers GC; Cader MZ; McLachlan RS Neurology; 2001 Oct; 57(8):1499-502. PubMed ID: 11673600 [TBL] [Abstract][Full Text] [Related]
12. Exercise-induced downbeat nystagmus in a Korean family with a nonsense mutation in CACNA1A. Choi JH; Seo JD; Choi YR; Kim MJ; Shin JH; Kim JS; Choi KD Neurol Sci; 2015 Aug; 36(8):1393-6. PubMed ID: 25784583 [TBL] [Abstract][Full Text] [Related]
13. Non-epileptic episodic disorders in young children. Bower BD Proc R Soc Med; 1974 May; 67(5):377-8. PubMed ID: 4835286 [No Abstract] [Full Text] [Related]
14. Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination. Wolf NI; Cundall M; Rutland P; Rosser E; Surtees R; Benton S; Chong WK; Malcolm S; Ebinger F; Bitner-Glindzicz M; Woodward KJ Neurogenetics; 2007 Jan; 8(1):39-44. PubMed ID: 16969684 [TBL] [Abstract][Full Text] [Related]
16. Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo). Brandt T; Strupp M Audiol Neurootol; 1997; 2(6):373-83. PubMed ID: 9390841 [TBL] [Abstract][Full Text] [Related]
17. [Positional nystagmus in patients with the vertigo syndrome]. Vela Colina M An Otorrinolaringol Ibero Am; 1984; 11(1):39-47. PubMed ID: 6476304 [No Abstract] [Full Text] [Related]
18. Positional vertigo and nystagmus. Barber HO Otolaryngol Clin North Am; 1973 Feb; 6(1):169-87. PubMed ID: 4220277 [No Abstract] [Full Text] [Related]
19. Familial episodic ataxia type II. Mugundhan K; Thiruvarutchelvan K; Sivakumar S J Assoc Physicians India; 2011 Oct; 59():668-70. PubMed ID: 22479753 [TBL] [Abstract][Full Text] [Related]
20. Novel missense variant of CACNA1A gene: A case report of a family with episodic ataxia type 2. Sivák Š; Kurča E; Krajčiová A; Hikkelová M; Šimko J; Mišovicová N; Kantorová E; Turčanová-Koprušáková M; Burjanivová T; Čierny D; Nosál' V J Neurol Sci; 2017 May; 376():119-120. PubMed ID: 28431595 [No Abstract] [Full Text] [Related] [Next] [New Search]