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Case Reports

Coincidental occurance of episodic ataxia and multiple sclerosis: a case report and review of the literature

ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon & ORCID Icon
Pages 656-661 | Received 26 Apr 2020, Accepted 05 Oct 2020, Published online: 20 Oct 2020

References

  • Marcel C, Anheim M, Flamand-Rouvière C, et al. Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases. J Neurol. 2010;257(8):1369–1372.
  • Spacey S. Episodic Ataxia Type 2. In: GeneReviews®. Seattle (WA): University of Washington, Seattle; 1993.
  • Consortium for Clinical Investigations of Neurological Channelopathies (CINCH) – consortiapedia.fastercures.org.
  • Choi K-D, Choi J-H. Episodic ataxias: clinical and genetic features. J Mov Disord. 2016;9(3):129–135.
  • Kaido M, Furuta M, Nakamori M, et al. Episodic ataxia type 2 manifests as epileptiform electroencephalographic activity with no epileptic attacks in two family members. Clin Neurol. 2016;56(4):260–264.
  • Mantuano E, Romano S, Veneziano L, et al. Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. J Neurol Sci. 2010;291(1-2):30–36.
  • Baloh RW, Yue Q, Furman JM, et al. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p. Ann Neurol. 1997;41(1):8–16.
  • Nachbauer W, Nocker M, Karner E, et al. Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature. J Neurol. 2014;261(5):983–991.
  • Subramony SH, Schott K, Raike RS, et al. Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits. Ann Neurol. 2003;54(6):725–731.
  • Vighetto A, Froment JC, Trillet M, et al. Magnetic resonance imaging in familial paroxysmal ataxia. Arch Neurol. 1988;45(5):547–549.
  • Casey HL, Gomez CM. Spinocerebellar Ataxia Type 6. 1998 Oct 23 [Updated 2019 Nov 21]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1140/
  • Battistini S, Stenirri S, Piatti M, et al. A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia. Neurology. 1999;53(1):38–43.
  • Ducros A, Denier C, Joutel A, et al. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia. Am J Hum Genet. 1999;64(1):89–98.
  • Friend KL, Crimmins D, Phan TG, et al. Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM. Hum Genet. 1999;105(3):261–265.

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