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Journal Abstract Search

400 related items for PubMed ID: 9779806

  • 1. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
    Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV.
    Am J Med Genet; 1998 Oct 12; 79(5):383-7. PubMed ID: 9779806
    [Abstract] [Full Text] [Related]

  • 2. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
    Hashida H, Goto J, Kurisaki H, Mizusawa H, Kanazawa I.
    Ann Neurol; 1997 Apr 12; 41(4):505-11. PubMed ID: 9124808
    [Abstract] [Full Text] [Related]

  • 3. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.
    Arch Neurol; 2004 Feb 12; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 4. Spinocerebellar ataxia type 2 in a Turkish family.
    Dirik E, Yiş U, Başak N, Soydan E, Hüdaoğlu O, Ozgönül F.
    J Child Neurol; 2007 Jul 12; 22(7):891-4. PubMed ID: 17715286
    [Abstract] [Full Text] [Related]

  • 5. The parkinsonian phenotype of spinocerebellar ataxia type 2.
    Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH.
    Arch Neurol; 2004 Jan 12; 61(1):35-8. PubMed ID: 14732617
    [Abstract] [Full Text] [Related]

  • 6. Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.
    Singh A, Faruq M, Mukerji M, Dwivedi MK, Pruthi S, Kapoor S.
    J Child Neurol; 2014 Jan 12; 29(1):139-44. PubMed ID: 24300164
    [Abstract] [Full Text] [Related]

  • 7. [Spinocerebellar ataxia type 7: clinical and molecular genetic analysis of a Mexican family].
    Rolón Lacarriere O, Rasmussen Almaraz A, Hernández Cruz H, Carranza del Río J, González Cruz M, Gutiérrez Moctezuma J.
    Rev Neurol; 2014 Jan 12; 38(8):736-40. PubMed ID: 15122543
    [Abstract] [Full Text] [Related]

  • 8. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
    Sanpei K, Takano H, Igarashi S, Sato T, Oyake M, Sasaki H, Wakisaka A, Tashiro K, Ishida Y, Ikeuchi T, Koide R, Saito M, Sato A, Tanaka T, Hanyu S, Takiyama Y, Nishizawa M, Shimizu N, Nomura Y, Segawa M, Iwabuchi K, Eguchi I, Tanaka H, Takahashi H, Tsuji S.
    Nat Genet; 1996 Nov 12; 14(3):277-84. PubMed ID: 8896556
    [Abstract] [Full Text] [Related]

  • 9. [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 Nov 12; 127(5-6):157-62. PubMed ID: 10500422
    [Abstract] [Full Text] [Related]

  • 10. Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7.
    Mao R, Aylsworth AS, Potter N, Wilson WG, Breningstall G, Wick MJ, Babovic-Vuksanovic D, Nance M, Patterson MC, Gomez CM, Snow K.
    Am J Med Genet; 2002 Jul 15; 110(4):338-45. PubMed ID: 12116207
    [Abstract] [Full Text] [Related]

  • 11. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
    Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S.
    Ann Neurol; 1997 Dec 15; 42(6):879-84. PubMed ID: 9403480
    [Abstract] [Full Text] [Related]

  • 12. Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis.
    Mutesa L, Pierquin G, Segers K, Vanbellinghen JF, Gahimbare L, Bours V.
    J Trop Pediatr; 2008 Oct 15; 54(5):350-2. PubMed ID: 18499737
    [Abstract] [Full Text] [Related]

  • 13. [Spinocerebellar ataxia type VII (AEC 7). Report of a Spanish family with the disease].
    Mayo D, Yusta A, Vázquez JM, García-Ruiz P, Robledo M, Benítez J.
    Rev Neurol; 2008 Oct 15; 28(10):964-6. PubMed ID: 10416231
    [Abstract] [Full Text] [Related]

  • 14. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
    Tashiro H, Suzuki SO, Hitotsumatsu T, Iwaki T.
    Clin Neuropathol; 1999 Oct 15; 18(4):198-204. PubMed ID: 10442462
    [Abstract] [Full Text] [Related]

  • 15. [A sporadic case of spinocerebellar ataxia 6 (SCA 6) with large CAG expansion of the CACNL1A4 gene].
    Izumi Y, Sawada H, Matsuyama Z, Kawakami H, Udaka F, Nakamura S, Kameyama M.
    No To Shinkei; 1999 Feb 15; 51(2):167-70. PubMed ID: 10198907
    [Abstract] [Full Text] [Related]

  • 16. [Autosomal dominant spinocerebellar ataxia].
    Legros B, Manto MU.
    Rev Med Brux; 1999 Dec 15; 20(6):495-503. PubMed ID: 10672773
    [Abstract] [Full Text] [Related]

  • 17. [Spinocerebellar ataxia 7. Clinical and genetic investigation in an Argentine family].
    Rojas JI, Romano M, Patrucco L, Zurru MC, Igarreta P, Cristiano E.
    Medicina (B Aires); 2007 Dec 15; 67(2):147-50. PubMed ID: 17593599
    [Abstract] [Full Text] [Related]

  • 18. Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2.
    Vinther-Jensen T, Ek J, Duno M, Skovby F, Hjermind LE, Nielsen JE, Nielsen TT.
    Eur J Hum Genet; 2013 Jun 15; 21(6):626-9. PubMed ID: 23047744
    [Abstract] [Full Text] [Related]

  • 19. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
    Hagenah JM, Zühlke C, Hellenbroich Y, Heide W, Klein C.
    Mov Disord; 2004 Feb 15; 19(2):217-20. PubMed ID: 14978680
    [Abstract] [Full Text] [Related]

  • 20. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
    Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, Sahba S.
    Nat Genet; 1996 Nov 15; 14(3):269-76. PubMed ID: 8896555
    [Abstract] [Full Text] [Related]

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