408 related articles for article (PubMed ID: 9403486)
1. 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]
2. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Schulz JB; Borkert J; Wolf S; Schmitz-Hübsch T; Rakowicz M; Mariotti C; Schöls L; Timmann D; van de Warrenburg B; Dürr A; Pandolfo M; Kang JS; Mandly AG; Nägele T; Grisoli M; Boguslawska R; Bauer P; Klockgether T; Hauser TK
Neuroimage; 2010 Jan; 49(1):158-68. PubMed ID: 19631275
[TBL] [Abstract][Full Text] [Related]
7. [Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory].
van de Warrenburg BP
Ned Tijdschr Geneeskd; 2001 May; 145(20):962-7. PubMed ID: 11396263
[TBL] [Abstract][Full Text] [Related]
8. 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; 42(6):879-84. PubMed ID: 9403480
[TBL] [Abstract][Full Text] [Related]
9. 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; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
10. Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlations.
Dubourg O; Dürr A; Cancel G; Stevanin G; Chneiweiss H; Penet C; Agid Y; Brice A
Ann Neurol; 1995 Feb; 37(2):176-80. PubMed ID: 7847859
[TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
Klockgether T; Skalej M; Wedekind D; Luft AR; Welte D; Schulz JB; Abele M; Bürk K; Laccone F; Brice A; Dichgans J
Brain; 1998 Sep; 121 ( Pt 9)():1687-93. PubMed ID: 9762957
[TBL] [Abstract][Full Text] [Related]
12. Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.
Rivaud-Pechoux S; Dürr A; Gaymard B; Cancel G; Ploner CJ; Agid Y; Brice A; Pierrot-Deseilligny C
Ann Neurol; 1998 Mar; 43(3):297-302. PubMed ID: 9506545
[TBL] [Abstract][Full Text] [Related]
13. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
Infante J; Combarros O; Volpini V; Corral J; Llorca J; Berciano J
Acta Neurol Scand; 2005 Jun; 111(6):391-9. PubMed ID: 15876341
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).
Dürr A; Brice A; Lepage-Lezin A; Cancel G; Smadja D; Vernant JC; Agid Y
Clin Neurosci; 1995; 3(1):12-6. PubMed ID: 7614088
[TBL] [Abstract][Full Text] [Related]
15. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
Rakowicz M; Zdzienicka E; Poniatowska R; Waliniowska E; Sułek A; Jakubowska T; Niedzielska K; Rola R; Wierzbicka A; Hoffman-Zacharska D; Głazowski C; Jakubczyk T; Niewiadomska M; Zaremba J
Neurol Neurochir Pol; 2005; 39(4):263-275. PubMed ID: 16096942
[TBL] [Abstract][Full Text] [Related]
16. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O
J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
[TBL] [Abstract][Full Text] [Related]
19. [Spinocerebellar ataxia: advances in genetic research and its clinical implication].
Sasaki H
Hokkaido Igaku Zasshi; 1997 Jan; 72(1):13-20. PubMed ID: 9086358
[TBL] [Abstract][Full Text] [Related]
20. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
Tang B; Wang D; Xia J
Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
