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Journal Abstract Search

138 related items for PubMed ID: 9859670

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. Familial episodic ataxia type II.
    Mugundhan K, Thiruvarutchelvan K, Sivakumar S.
    J Assoc Physicians India; 2011 Oct; 59():668-70. PubMed ID: 22479753
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 11(2):187-9. PubMed ID: 12525875
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7. Late onset hereditary episodic ataxia.
    Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K.
    J Neurol Neurosurg Psychiatry; 2009 May 15; 80(5):566-8. PubMed ID: 19372292
    [Abstract] [Full Text] [Related]

  • 8.
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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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 11. Episodic ataxia type 2: an uncommon inherited CNS channelopathies.
    Pulkes T.
    J Med Assoc Thai; 2003 Apr 15; 86(4):376-80. PubMed ID: 12757085
    [Abstract] [Full Text] [Related]

  • 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 Apr 15; 60(1):16-20. PubMed ID: 18437043
    [Abstract] [Full Text] [Related]

  • 13. [Familial paroxysmal ataxia responsive to acetazolamide].
    Aimard G, Vighetto A, Trillet M, Ventre JJ, Devic M.
    Rev Neurol (Paris); 1983 Apr 15; 139(4):251-8. PubMed ID: 6612140
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 15. [A case of spinocerebellar ataxia 6 accompanied with schizophrenia].
    Nakanishi I, Miwa H, Hayata T, Kawada A, Kondo T.
    No To Shinkei; 2004 Jan 01; 56(1):49-52. PubMed ID: 15024829
    [Abstract] [Full Text] [Related]

  • 16. CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2.
    Robbins MS, Lipton RB, Laureta EC, Grosberg BM.
    Headache; 2009 Jul 01; 49(7):1042-6. PubMed ID: 19486177
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 54(6):725-31. PubMed ID: 14681882
    [Abstract] [Full Text] [Related]

  • 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 Dec 01; 127(5-6):157-62. PubMed ID: 10500422
    [Abstract] [Full Text] [Related]

  • 19. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH.
    Am J Med Genet; 2002 May 08; 114(4):450-7. PubMed ID: 11992570
    [Abstract] [Full Text] [Related]

  • 20. Large CACNA1A deletion in a family with episodic ataxia type 2.
    Riant F, Mourtada R, Saugier-Veber P, Tournier-Lasserve E.
    Arch Neurol; 2008 Jun 08; 65(6):817-20. PubMed ID: 18541804
    [Abstract] [Full Text] [Related]

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