Literature DB >> 16972120

Spinocerebellar ataxia type 17 in a patient from an Indian kindred.

Dietrich Haubenberger, Daniela Prayer, Peter Bauer, Walter Pirker, Alexander Zimprich, Eduard Auff.   

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Year:  2006        PMID： 16972120     DOI： 10.1007/s00415-006-0265-1

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  15 in total

1.  Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype.

Authors:  P Bauer; F Laccone; A Rolfs; U Wüllner; S Bösch; H Peters; S Liebscher; M Scheible; J T Epplen; B H F Weber; E Holinski-Feder; H Weirich-Schwaiger; D J Morris-Rosendahl; J Andrich; O Riess
Journal:  J Med Genet       Date:  2004-03       Impact factor: 6.318

2.  FXTAS, SCA10, and SCA17 in American patients with movement disorders.

Authors:  Ana I Seixas; Martin H Maurer; Mark Lin; Colleen Callahan; Alka Ahuja; Tohru Matsuura; Christopher A Ross; Fuki M Hisama; Isabel Silveira; Russell L Margolis
Journal:  Am J Med Genet A       Date:  2005-07-01       Impact factor: 2.802

3.  Hyperintense putaminal rim sign is not a hallmark of multiple system atrophy at 3T.

Authors:  Wei-Hsing Lee; Chau-Chin Lee; Woei-Cherng Shyu; Pau-Nyen Chong; Shinn-Zong Lin
Journal:  AJNR Am J Neuroradiol       Date:  2005-10       Impact factor: 3.825

4.  CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

Authors:  H Fujigasaki; J J Martin; P P De Deyn; A Camuzat; D Deffond; G Stevanin; B Dermaut; C Van Broeckhoven; A Dürr; A Brice
Journal:  Brain       Date:  2001-10       Impact factor: 13.501

Review 5.  TATA-binding protein in neurodegenerative disease.

Authors:  W M C van Roon-Mom; S J Reid; R L M Faull; R G Snell
Journal:  Neuroscience       Date:  2005       Impact factor: 3.590

6.  Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging.

Authors:  Clement T Loy; Mary G Sweeney; Mary B Davis; Adrian J Wills; Guy V Sawle; Andrew J Lees; Sarah J Tabrizi
Journal:  Mov Disord       Date:  2005-11       Impact factor: 10.338

7.  Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.

Authors:  Y R Wu; H Y Lin; C M Chen; K Gwinn-Hardy; L S Ro; Y C Wang; S H Li; J C Hwang; K Fang; H M Hsieh-Li; M L Li; L C Tung; M T Su; K T Lu; G J Lee-Chen
Journal:  Clin Genet       Date:  2004-03       Impact factor: 4.438

8.  Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Authors:  K K Sinha; P F Worth; D K Jha; S Sinha; V J Stinton; M B Davis; N W Wood; M G Sweeney; K P Bhatia
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-03       Impact factor: 10.154

9.  Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).

Authors:  Arndt Rolfs; Arnulf H Koeppen; Ingrid Bauer; Peter Bauer; Sven Buhlmann; Helge Topka; Ludger Schöls; Olaf Riess
Journal:  Ann Neurol       Date:  2003-09       Impact factor: 10.422

10.  Clinical usefulness of magnetic resonance imaging in multiple system atrophy.

Authors:  A Schrag; D Kingsley; C Phatouros; C J Mathias; A J Lees; S E Daniel; N P Quinn
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-07       Impact factor: 10.154
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