106 related articles for article (PubMed ID: 10416231)
1. [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; 1999 May 16-31; 28(10):964-6. PubMed ID: 10416231
[TBL] [Abstract][Full Text] [Related]
2. [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; 2004 Apr 16-30; 38(8):736-40. PubMed ID: 15122543
[TBL] [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; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
4. Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.
Bauer PO; Matoska V; Zumrova A; Boday A; Doi H; Marikova T; Goetz P
J Appl Genet; 2005; 46(3):325-8. PubMed ID: 16110192
[TBL] [Abstract][Full Text] [Related]
5. [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; 67(2):147-50. PubMed ID: 17593599
[TBL] [Abstract][Full Text] [Related]
6. 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; 79(5):383-7. PubMed ID: 9779806
[TBL] [Abstract][Full Text] [Related]
7. The parkinsonian phenotype of spinocerebellar ataxia type 2.
Lu CS; Wu Chou YH; Kuo PC; Chang HC; Weng YH
Arch Neurol; 2004 Jan; 61(1):35-8. PubMed ID: 14732617
[TBL] [Abstract][Full Text] [Related]
8. 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; 22(7):891-4. PubMed ID: 17715286
[TBL] [Abstract][Full Text] [Related]
9. 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; 54(5):350-2. PubMed ID: 18499737
[TBL] [Abstract][Full Text] [Related]
10. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region.
Hellenbroich Y; Bubel S; Pawlack H; Opitz S; Vieregge P; Schwinger E; Zühlke C
J Neurol; 2003 Jun; 250(6):668-71. PubMed ID: 12796826
[TBL] [Abstract][Full Text] [Related]
11. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE
J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805
[TBL] [Abstract][Full Text] [Related]
12. Fluorescent multiplex PCR--fast method for autosomal dominant spinocerebellar ataxias screening.
Bauer PO; Kotliarova SE; Matoska V; Musova Z; Hedvicakova P; Boday A; Tomek A; Nukina N; Goetz P
Genetika; 2005 Jun; 41(6):830-7. PubMed ID: 16080609
[TBL] [Abstract][Full Text] [Related]
13. Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.
Tachikawa M; Nagai Y; Nakamura K; Kobayashi K; Fujiwara T; Han HJ; Nakabayashi Y; Ichikawa Y; Goto J; Kanazawa I; Nakamura Y; Toda T
J Hum Genet; 2002; 47(6):275-8. PubMed ID: 12111376
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Clinical features of autosomal dominant spinocerebellar ataxias genetically unclassified into any known triplet-repeat diseases].
Aoki K; Kawata A; Suda M; Hirai S
Rinsho Shinkeigaku; 2001 Jan; 41(1):18-23. PubMed ID: 11433762
[TBL] [Abstract][Full Text] [Related]
16. [Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Liang XC; Tang JG
Zhonghua Yi Xue Za Zhi; 2006 Jul; 86(25):1755-8. PubMed ID: 17054842
[TBL] [Abstract][Full Text] [Related]
17. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
Hugosson T; Gränse L; Ponjavic V; Andréasson S
Ophthalmic Genet; 2009 Mar; 30(1):1-6. PubMed ID: 19172503
[TBL] [Abstract][Full Text] [Related]
18. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A
Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117
[TBL] [Abstract][Full Text] [Related]
19. [Clinical and genetic studies of a family from Peru affected by spinocerebellar ataxia type 7].
Castañeda MA; Avalos C; Jerí FR
Rev Neurol; 2000 Nov 16-30; 31(10):923-8. PubMed ID: 11244684
[TBL] [Abstract][Full Text] [Related]
20. [Type 8 spinocerebellar ataxia. A report of a family].
Sempere AP; Millán JM; Royo-Vilanova C; Medrano V
Rev Neurol; 2001 Jul 16-31; 33(2):150-2. PubMed ID: 11562876
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]