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Journal Abstract Search

226 related items for PubMed ID: 12525875

  • 1. 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
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  • 2. Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
    Subramony SH, Schott K, Raike RS, Callahan J, Langford LR, Christova PS, Anderson JH, Gomez CM.
    Ann Neurol; 2003 Dec; 54(6):725-31. PubMed ID: 14681882
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  • 13. Missense CACNA1A mutation causing episodic ataxia type 2.
    Denier C, Ducros A, Durr A, Eymard B, Chassande B, Tournier-Lasserve E.
    Arch Neurol; 2001 Feb; 58(2):292-5. PubMed ID: 11176968
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  • 14. Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
    Imbrici P, Jaffe SL, Eunson LH, Davies NP, Herd C, Robertson R, Kullmann DM, Hanna MG.
    Brain; 2004 Dec; 127(Pt 12):2682-92. PubMed ID: 15483044
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  • 15. [Familial episodic ataxia type 2. Clinical and genetic study of one family].
    Suárez-Cuervo A, Salas-Puig J, Alvarez V, Coto E, Fernández JM, Lahoz CH.
    Neurologia; 1998 Oct; 13(8):382-7. PubMed ID: 9859670
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  • 20. 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
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