Publications by authors named "Thorsten Schulte"

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Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias.
Kathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, Juliane Vollmer-Haase, Peter Bauer, Thorsten Schulte

Mov Disord· November 2004

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Mutation at the SCA17 locus is not a common cause of primary dystonia.
Kathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, Juliane Vollmer-Haase, Peter Bauer, Thorsten Schulte

J Neurol· October 2004

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Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess

Lancet Neurol· May 2004

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Treatment benefit and daily drug costs associated with treating Parkinson's disease in a Parkinson's disease clinic.
Thomas Müller, Birgit Voss, Kerstin Hellwig, Franz Josef Stein, Thorsten Schulte

CNS Drugs· March 2004

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Mutation analysis of the neurofilament M gene in Parkinson's disease.
Rejko Krüger, Christian Fischer, Thorsten Schulte, Karsten M Strauss, Thomas Müller

Neurosci Lett· November 2003

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Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.
Kathrin Grundmann, Ulrike Laubis-Herrmann, Ingrid Bauer, Dirk Dressler, Juliane Vollmer-Haase, Thorsten Schulte

Arch Neurol· September 2003

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Do CTG expansions at the SCA8 locus cause ataxia?
Ludger Schöls, Ingrid Bauer, Christine Zühlke, Thorsten Schulte, Christina Kölmel

Ann Neurol· July 2003

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Intravenous amantadine sulphate application improves the performance of complex but not simple motor tasks in patients with Parkinson's disease.
Thomas Müller, Wilfried Kuhn, Thorsten Schulte, Horst Przuntek

Neurosci Lett· March 2003

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Polymorphisms in the interleukin-1 alpha and beta genes and the risk for Parkinson's disease.
Thorsten Schulte, Ludger Schöls, Thomas Müller, Dirk Woitalla, Klaus Berger

Neurosci Lett· June 2002

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