192 related articles for article (PubMed ID: 14628900)
1. Dominant spinocerebellar ataxias: a molecular approach to classification, diagnosis, pathogenesis and the future.
Margolis RL
Expert Rev Mol Diagn; 2003 Nov; 3(6):715-32. PubMed ID: 14628900
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Spinocerebellar ataxias: an update.
Soong BW; Paulson HL
Curr Opin Neurol; 2007 Aug; 20(4):438-46. PubMed ID: 17620880
[TBL] [Abstract][Full Text] [Related]
4. [Hereditary ataxias-overview].
Nishizawa M
Rinsho Shinkeigaku; 2001 Dec; 41(12):1114-6. PubMed ID: 12235812
[TBL] [Abstract][Full Text] [Related]
5. Dynamic mutation and human disorders: the spinocerebellar ataxias (review).
Costa Lima MA; Pimentel MM
Int J Mol Med; 2004 Feb; 13(2):299-302. PubMed ID: 14719138
[TBL] [Abstract][Full Text] [Related]
6. Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy.
Michalik A; Martin JJ; Van Broeckhoven C
Eur J Hum Genet; 2004 Jan; 12(1):2-15. PubMed ID: 14571264
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3.
Paulson HL
Semin Neurol; 2007 Apr; 27(2):133-42. PubMed ID: 17390258
[TBL] [Abstract][Full Text] [Related]
9. [Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type 7].
Xie QY; Liang XL; Li XH; Feng YQ
Di Yi Jun Yi Da Xue Xue Bao; 2004 Jan; 24(1):62-5. PubMed ID: 14724100
[TBL] [Abstract][Full Text] [Related]
10. Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias.
Seneca S; Morris MA; Patton S; Elles R; Sequeiros J
Eur J Hum Genet; 2008 Aug; 16(8):913-20. PubMed ID: 18301445
[TBL] [Abstract][Full Text] [Related]
11. Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology.
Stevanin G; Dürr A; Brice A
Eur J Hum Genet; 2000 Jan; 8(1):4-18. PubMed ID: 10713882
[TBL] [Abstract][Full Text] [Related]
12. Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirable.
Gupta SN; Marks HG
J Neurol Sci; 2008 Jan; 264(1-2):173-6. PubMed ID: 17720198
[TBL] [Abstract][Full Text] [Related]
13. [Autosomal dominant spinocerebellar ataxia].
Milewska D; Hoffman-Zacharska D; Zaremba J
Neurol Neurochir Pol; 1999; 33(3):633-43. PubMed ID: 10540724
[TBL] [Abstract][Full Text] [Related]
14. Pathogenesis of polyglutamine disorders: aggregation revisited.
Michalik A; Van Broeckhoven C
Hum Mol Genet; 2003 Oct; 12 Spec No 2():R173-86. PubMed ID: 14504263
[TBL] [Abstract][Full Text] [Related]
15. [The genetics of spinocerebellar ataxias].
Jacobi H; Minnerop M; Klockgether T
Nervenarzt; 2013 Feb; 84(2):137-42. PubMed ID: 23338152
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].
Xie QY; Liang XL; Li XH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):71-3. PubMed ID: 15696485
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Spinocerebellar ataxia type 17: latest member of polyglutamine disease group highlights unanswered questions.
Tsuji S
Arch Neurol; 2004 Feb; 61(2):183-4. PubMed ID: 14967764
[No Abstract] [Full Text] [Related]
20. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Schöls L; Bauer P; Schmidt T; Schulte T; Riess O
Lancet Neurol; 2004 May; 3(5):291-304. PubMed ID: 15099544
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]