BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 16109427)

  • 1. Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations.
    Kerber KA; Jen JC; Perlman S; Baloh RW
    J Neurol Sci; 2005 Nov; 238(1-2):41-5. PubMed ID: 16109427
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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; 127(5-6):157-62. PubMed ID: 10500422
    [TBL] [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; 254(1-2):69-71. PubMed ID: 17292920
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
    Schöls L; Amoiridis G; Büttner T; Przuntek H; Epplen JT; Riess O
    Ann Neurol; 1997 Dec; 42(6):924-32. PubMed ID: 9403486
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
    Yabe I; Sasaki H; Yamashita I; Takei A; Fukazawa T; Hamada T; Tashiro K
    Rinsho Shinkeigaku; 1998 Jun; 38(6):489-94. PubMed ID: 9847664
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fragile X premutation with atypical symptoms at onset.
    Cellini E; Forleo P; Ginestroni A; Nacmias B; Tedde A; Bagnoli S; Mascalchi M; Sorbi S; Piacentini S
    Arch Neurol; 2006 Aug; 63(8):1135-8. PubMed ID: 16908740
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
    Gomez CM; Thompson RM; Gammack JT; Perlman SL; Dobyns WB; Truwit CL; Zee DS; Clark HB; Anderson JH
    Ann Neurol; 1997 Dec; 42(6):933-50. PubMed ID: 9403487
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
    Lee WY; Jin DK; Oh MR; Lee JE; Song SM; Lee EA; Kim GM; Chung JS; Lee KH
    Arch Neurol; 2003 Jun; 60(6):858-63. PubMed ID: 12810491
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Late cerebellar ataxia associated with fragile X premutation].
    Chaussenot A; Borg M; Bayreuther C; Lebrun C
    Rev Neurol (Paris); 2008 Nov; 164(11):957-63. PubMed ID: 18808779
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxia.
    Adams SA; Steenblock KJ; Thibodeau SN; Lindor NM
    J Neurogenet; 2008; 22(1):77-92. PubMed ID: 18363164
    [TBL] [Abstract][Full Text] [Related]  

  • 11. FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.
    Brussino A; Gellera C; Saluto A; Mariotti C; Arduino C; Castellotti B; Camerlingo M; de Angelis V; Orsi L; Tosca P; Migone N; Taroni F; Brusco A
    Neurology; 2005 Jan; 64(1):145-7. PubMed ID: 15642922
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Positional vertigo and macroscopic downbeat positioning nystagmus in spinocerebellar ataxia type 6 (SCA6).
    Yabe I; Sasaki H; Takeichi N; Takei A; Hamada T; Fukushima K; Tashiro K
    J Neurol; 2003 Apr; 250(4):440-3. PubMed ID: 12700909
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 60(1):16-20. PubMed ID: 18437043
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
    Peters N; Kamm C; Asmus F; Holinski-Feder E; Kraft E; Dichgans M; Brüning R; Gasser T; Bötzel K
    Mov Disord; 2006 Jan; 21(1):98-102. PubMed ID: 16124012
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Differential diagnosis of spinocerebellar ataxia].
    Sasaki H
    Rinsho Shinkeigaku; 2002 Nov; 42(11):1069-72. PubMed ID: 12784668
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
    Schmitz-Hübsch T; Coudert M; Bauer P; Giunti P; Globas C; Baliko L; Filla A; Mariotti C; Rakowicz M; Charles P; Ribai P; Szymanski S; Infante J; van de Warrenburg BP; Dürr A; Timmann D; Boesch S; Fancellu R; Rola R; Depondt C; Schöls L; Zdienicka E; Kang JS; Döhlinger S; Kremer B; Stephenson DA; Melegh B; Pandolfo M; di Donato S; du Montcel ST; Klockgether T
    Neurology; 2008 Sep; 71(13):982-9. PubMed ID: 18685131
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [An apparently sporadic case with spinocerebellar ataxia type 1 (SCA1)].
    Futamura N; Matsumura R; Murata K; Suzumura A; Takayanagi T
    Rinsho Shinkeigaku; 1997 Aug; 37(8):708-10. PubMed ID: 9404150
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
    Hiramoto K; Kawakami H; Inoue K; Seki T; Maruyama H; Morino H; Matsumoto M; Kurisu K; Sakai N
    Mov Disord; 2006 Sep; 21(9):1355-60. PubMed ID: 16763984
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.
    Imbrici P; Eunson LH; Graves TD; Bhatia KP; Wadia NH; Kullmann DM; Hanna MG
    Neurology; 2005 Sep; 65(6):944-6. PubMed ID: 16186543
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oculomotor abnormalities in myoclonic tremor: a comparison with spinocerebellar ataxia type 6.
    Bour LJ; van Rootselaar AF; Koelman JH; Tijssen MA
    Brain; 2008 Sep; 131(Pt 9):2295-303. PubMed ID: 18687731
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.