Literature DB >> 15258801

Basal ganglia involvement of a patient with SCA 17--a new form of autosomal dominant spinocerebellar ataxia.

P Günther, A Storch, J Schwarz, O Sabri, P Steinbach, A Wagner, S Hesse.   

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Year:  2004        PMID： 15258801     DOI： 10.1007/s00415-004-0462-8

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


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  7 in total

1.  SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.

Authors:  K Nakamura; S Y Jeong; T Uchihara; M Anno; K Nagashima; T Nagashima; S Ikeda; S Tsuji; I Kanazawa
Journal:  Hum Mol Genet       Date:  2001-07-01       Impact factor: 6.150

2.  Striatal dopamine transporter binding in early to moderately advanced Parkinson's disease: monitoring of disease progression over 2 years.

Authors:  M Chouker; K Tatsch; R Linke; O Pogarell; K Hahn; J Schwarz
Journal:  Nucl Med Commun       Date:  2001-06       Impact factor: 1.690

3.  Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

Authors:  I Silveira; C Miranda; L Guimarães; M-C Moreira; I Alonso; P Mendonça; A Ferro; J Pinto-Basto; J Coelho; F Ferreirinha; J Poirier; E Parreira; J Vale; C Januário; C Barbot; A Tuna; J Barros; R Koide; S Tsuji; S E Holmes; R L Margolis; L Jardim; M Pandolfo; P Coutinho; J Sequeiros
Journal:  Arch Neurol       Date:  2002-04

4.  Investigating dopaminergic neurotransmission with 123I-FP-CIT SPECT: comparability of modern SPECT systems.

Authors:  Philipp T Meyer; Bernhard Sattler; Thomas Lincke; Anita Seese; Osama Sabri
Journal:  J Nucl Med       Date:  2003-05       Impact factor: 10.057

5.  Mutation at the SCA17 locus is not a common cause of parkinsonism.

Authors:  Dena Hernandez; Melissa Hanson; Amanda Singleton; Katrina Gwinn-Hardy; Jason Freeman; Bernard Ravina; Dana Doheny; Marisol Gallardo; Roberto Weiser; John Hardy; Andrew Singleton
Journal:  Parkinsonism Relat Disord       Date:  2003-08       Impact factor: 4.891

6.  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

7.  Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Authors:  Giovanni Stevanin; Hiroto Fujigasaki; Anne-Sophie Lebre; Agnes Camuzat; Cecile Jeannequin; Catherine Dode; Junko Takahashi; Chankranira San; Robert Bellance; Alexis Brice; Alexandra Durr
Journal:  Brain       Date:  2003-05-06       Impact factor: 13.501
  7 in total
  8 in total

1.  Vascular parkinsonism in a CADASIL case with an intact nigrostriatal dopaminergic system.

Authors:  F Wegner; K Strecker; J Schwarz; A Wagner; W Heinritz; F Sommerer; D R Thal; J-P Schneider; K Kendziorra; O Sabri
Journal:  J Neurol       Date:  2007-11-21       Impact factor: 4.849

2.  Intact serotonergic and dopaminergic systems in two cases of orthostatic tremor.

Authors:  F Wegner; K Strecker; D Boeckler; A Wagner; Ch Preul; D Lobsien; O Sabri; S Hesse
Journal:  J Neurol       Date:  2008-09-25       Impact factor: 4.849

3.  Magnetic resonance imaging in spinocerebellar ataxias.

Authors:  Susanne Döhlinger; Till-Karsten Hauser; Johannes Borkert; Andreas R Luft; Jörg B Schulz
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

4.  Investigating function and connectivity of morphometric findings--exemplified on cerebellar atrophy in spinocerebellar ataxia 17 (SCA17).

Authors:  Kathrin Reetz; Imis Dogan; Arndt Rolfs; Ferdinand Binkofski; Jörg B Schulz; Angela R Laird; Peter T Fox; Simon B Eickhoff
Journal:  Neuroimage       Date:  2012-05-30       Impact factor: 6.556

5.  Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.

Authors:  Kathrin Reetz; Rebekka Lencer; Johannes M Hagenah; Christian Gaser; Vera Tadic; Uwe Walter; Alexander Wolters; Susanne Steinlechner; Christine Zühlke; Katja Brockmann; Christine Klein; Arndt Rolfs; Ferdinand Binkofski
Journal:  Cerebellum       Date:  2010-06       Impact factor: 3.847

6.  Nigrostriatal involvement in ataxia with oculomotor apraxia type 1.

Authors:  Elena Salvatore; Andrea Varrone; Chiara Criscuolo; Pietro Mancini; Valeria Sansone; Caterina Strisciuglio; Domenico Cicala; Valencia Scarano; Marco Salvatore; Sabina Pappatà; Giuseppe De Michele; Alessandro Filla
Journal:  J Neurol       Date:  2007-11-21       Impact factor: 4.849

Review 7.  Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein.

Authors:  Christine Zühlke; Katrin Bürk
Journal:  Cerebellum       Date:  2007-01-19       Impact factor: 3.847

8.  Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patients.

Authors:  Caterina Mariotti; Dario Alpini; Roberto Fancellu; Paola Soliveri; Marina Grisoli; Sabrina Ravaglia; Carlo Lovati; Vincenza Fetoni; Giorgio Giaccone; Alessia Castucci; Franco Taroni; Cinzia Gellera; Stefano Di Donato
Journal:  J Neurol       Date:  2007-10-15       Impact factor: 4.849
  8 in total

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