Sylvia Boesch

Best Publications

• Scale for the assessment and rating of ataxia: development of a new clinical scale.

  T Schmitz-Hübsch;S Tezenas du Montcel;L Baliko;J Berciano

  2130
  Citations

• The natural history of multiple system atrophy: a prospective European cohort study

  Gregor K Wenning;Felix Geser;Felix Geser;Florian Krismer;Klaus Seppi

  590
  Citations

• Diagnosis and treatment of Friedreich ataxia: a European perspective

  Jörg B. Schulz;Sylvia Boesch;Katrin Bürk;Alexandra Dürr

  347
  Citations

• Clinical features of Friedreich's ataxia: Classical and atypical phenotypes

  Michael H. Parkinson;Sylvia Boesch;Wolfgang Nachbauer;Caterina Mariotti

  342
  Citations

• Spinocerebellar ataxia types 1, 2, 3, and 6 Disease severity and nonataxia symptoms

  T Schmitz-Hübsch;M Coudert;Peter Bauer;P Giunti

  309
  Citations

• Presentation, diagnosis, and management of multiple system atrophy in Europe: Final analysis of the European multiple system atrophy registry

  Martin Köllensperger;Felix Geser;Jean Pierre Ndayisaba;Sylvia Boesch

  303
  Citations

• Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

  Heike Jacobi;Sophie Tezenas du Montcel;Peter Bauer;Paola Giunti

  300
  Citations

• Diffusion-weighted imaging discriminates progressive supranuclear palsy from PD, but not from the parkinson variant of multiple system atrophy

  K. Seppi;M.F.H. Schocke;R. Esterhammer;C. Kremser

  291
  Citations

• Red flags for multiple system atrophy

  Martin Köllensperger;Felix Geser;Klaus Seppi;Michaela Stampfer-Kountchev

  274
  Citations

• Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (MOXIe Study).

  David R Lynch;Melanie P Chin;Martin B Delatycki;S H Subramony

  269
  Citations

• The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study

  H. Jacobi;P. Bauer;P. Giunti;R. Labrum

  241
  Citations

• Consensus Paper: Management of Degenerative Cerebellar Disorders

  W. Ilg;A. J. Bastian;S. Boesch;R. G. Burciu

  232
  Citations

• Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: A cross-sectional analysis of baseline data

  Kathrin Reetz;Imis Dogan;Imis Dogan;Ana S Costa;Manuel Dafotakis

  232
  Citations

• Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data

  Heike Jacobi;Kathrin Reetz;Kathrin Reetz;Sophie Tezenas du Montcel;Peter Bauer

  205
  Citations

• Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients

  Tanja T. Schmitz-Hübsch;Sophie Tezenas S.T. du Montcel;Laszlo L. Baliko;Sylvia S. Boesch

  202
  Citations

• Monogenic variants in dystonia: an exome-wide sequencing study.

  Michael Zech;Robert Jech;Sylvia Boesch;Matej Škorvánek

  199
  Citations

• Dystonia in multiple system atrophy

  S M Boesch;G K Wenning;G Ransmayr;W Poewe

  198
  Citations

• Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

  Sophie Tezenas Du Montcel;Sophie Tezenas Du Montcel;Alexandra Durr;Peter Bauer;Karla P. Figueroa

  194
  Citations

• Comparison of three clinical rating scales in Friedreich ataxia (FRDA).

  Katrin Bürk;Katrin Bürk;Ulrike Mälzig;Stefanie Wolf;Suzette Heck

  194
  Citations

• Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

  Christoph Globas;Sophie Tezenas du Montcel;Laslo Baliko;Syliva Boesch

  192
  Citations