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PUBMED FOR HANDHELDS

Journal Abstract Search


352 related items for PubMed ID: 29883219

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  • 7. 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
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  • 8. 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 26; 20(1):155. PubMed ID: 32336275
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  • 10. 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 15; 291(1-2):30-6. PubMed ID: 20129625
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  • 14. Clinical spectrum of episodic ataxia type 2.
    Jen J, Kim GW, Baloh RW.
    Neurology; 2004 Jan 13; 62(1):17-22. PubMed ID: 14718690
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  • 15. What Is Behind Cerebellar Vertigo and Dizziness?
    Feil K, Strobl R, Schindler A, Krafczyk S, Goldschagg N, Frenzel C, Glaser M, Schöberl F, Zwergal A, Strupp M.
    Cerebellum; 2019 Jun 13; 18(3):320-332. PubMed ID: 30552638
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  • 16. Slowed abduction during smooth pursuit eye movement in episodic ataxia type 2 with a novel CACNA1A mutation.
    Shimmura M, Uehara T, Yamashita K, Shigeto H, Yamasaki R, Ishikawa K, Kira JI.
    J Neurol Sci; 2017 Oct 15; 381():4-6. PubMed ID: 28991713
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  • 17. Novel CACNA1A mutation(s) associated with slow saccade velocities.
    Kipfer S, Jung S, Lemke JR, Kipfer-Kauer A, Howell JP, Kaelin-Lang A, Nyffeler T, Gutbrod K, Abicht A, Müri RM.
    J Neurol; 2013 Dec 15; 260(12):3010-4. PubMed ID: 24046065
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  • 19. 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 15; 268(11):4296-4302. PubMed ID: 33983550
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