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Journal Abstract Search

138 related items for PubMed ID: 9859670

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  • 3. 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 15; 254(1-2):69-71. PubMed ID: 17292920
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  • 4. [Acute intermittent familial ataxia: report of a new family].
    Pérez-Rodríguez MJ, Lorenzo-Sanz G, Aparicio-Meix JM.
    Rev Neurol; 1996 May 15; 24(129):570-1. PubMed ID: 8681177
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  • 6. 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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  • 9. [Hereditary episodic ataxia].
    Riant F, Vahedi K, Tournier-Lasserve E.
    Rev Neurol (Paris); 2011 May 15; 167(5):401-7. PubMed ID: 21492892
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  • 10. [Familial paroxysmal ataxia: a new case].
    Escribano JB, Moltó JM, Martínez-García FA, Morales A, Jiménez-Martínez JM, Fernández-Barreiro A.
    Rev Neurol; 1996 May 15; 24(129):567-9. PubMed ID: 8681176
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  • 12. Progressive cerebellar ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation.
    Marti S, Baloh RW, Jen JC, Straumann D, Jung HH.
    Eur Neurol; 2008 May 15; 60(1):16-20. PubMed ID: 18437043
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  • 14. X-linked congenital ataxia: a clinical and genetic study.
    Bertini E, des Portes V, Zanni G, Santorelli F, Dionisi-Vici C, Vicari S, Fariello G, Chelly J.
    Am J Med Genet; 2000 May 01; 92(1):53-6. PubMed ID: 10797423
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  • 18. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M, Culjković B, Sternić N, Dragasević B, Stojković I, Romac S, Kostić VS.
    Srp Arh Celok Lek; 1999 May 01; 127(5-6):157-62. PubMed ID: 10500422
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