S
Sylvia Boesch
Researcher at Innsbruck Medical University
Publications - 143
Citations - 5713
Sylvia Boesch is an academic researcher from Innsbruck Medical University. The author has contributed to research in topics: Ataxia & Medicine. The author has an hindex of 37, co-authored 122 publications receiving 4509 citations.
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Journal ArticleDOI
The natural history of multiple system atrophy: a prospective European cohort study
Gregor K. Wenning,Felix Geser,Felix Geser,Florian Krismer,Klaus Seppi,Susanne Duerr,Sylvia Boesch,Martin Köllensperger,Georg Goebel,Karl P. Pfeiffer,Karl P. Pfeiffer,Paolo Barone,Maria Teresa Pellecchia,Niall Quinn,Vasiliki Koukouni,Clare J. Fowler,Anette Schrag,Christopher J. Mathias,Nir Giladi,Tanya Gurevich,Erik Dupont,Karen Østergaard,Christer Nilsson,Håkan Widner,Wolfgang H. Oertel,Karla Eggert,Alberto Albanese,Francesca Del Sorbo,Eduardo Tolosa,Adriana Cardozo,Günther Deuschl,Helge Hellriegel,Thomas Klockgether,Richard Dodel,Cristina Sampaio,Miguel Coelho,Ruth Djaldetti,Eldad Melamed,Thomas Gasser,Christoph Kamm,Christoph Kamm,Giuseppe Meco,Carlo Colosimo,Olivier Rascol,Wassilios G. Meissner,François Tison,Werner Poewe +46 more
TL;DR: The final analysis of a prospective multicentre study by the European MSA Study Group provides new insights into the evolution of MSA based on a follow-up period that exceeds that of previous studies.
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Diffusion-weighted imaging discriminates progressive supranuclear palsy from PD, but not from the parkinson variant of multiple system atrophy
Klaus Seppi,Michael Schocke,Regina Esterhammer,Christian Kremser,Christian Brenneis,Joerg Mueller,Sylvia Boesch,Werner Jaschke,Werner Poewe,Gregor K. Wenning +9 more
TL;DR: Results show that DWI detects basal ganglia abnormalities in PSP patients within few years of disease onset, discriminating patients with PSP from those with PD, but not fromThose with MSA-P.
Journal ArticleDOI
Diagnosis and treatment of Friedreich ataxia: a European perspective
Jörg B. Schulz,Sylvia Boesch,Katrin Bürk,Alexandra Durr,Paola Giunti,Caterina Mariotti,Françoise Pousset,Ludger Schöls,Pierre Vankan,Massimo Pandolfo +9 more
TL;DR: This Review provides guidelines, from a European perspective, for the diagnosis of Friedreich ataxia, differential diagnosis of ataxias and genetic counseling, and treatment of neurological and non-neurological symptoms.
Journal ArticleDOI
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,Arron Cook,Robyn Labrum,Michael H Parkinson,Alexandra Durr,Alexis Brice,Perrine Charles,Cecilia Marelli,Caterina Mariotti,Lorenzo Nanetti,Marta Panzeri,Maria Rakowicz,Anna Sulek,Anna Sobanska,Tanja Schmitz-Hübsch,Ludger Schöls,Ludger Schöls,Holger Hengel,Holger Hengel,Laszlo Baliko,Béla Melegh,Alessandro Filla,Antonella Antenora,Jon Infante,José Berciano,Bart P.C. van de Warrenburg,Dagmar Timmann,Sandra Szymanski,Sylvia Boesch,Jun Suk Kang,Massimo Pandolfo,Jörg B. Schulz,Sonia Molho,Alhassane Diallo,Thomas Klockgether,Thomas Klockgether +38 more
TL;DR: This study provides quantitative data on the progression of the most common spinocerebellar ataxias based on a follow-up period that exceeds those of previous studies and could prove useful for sample size calculation and patient stratification in interventional trials.
Journal ArticleDOI
Red flags for multiple system atrophy
Martin Köllensperger,Felix Geser,Klaus Seppi,Michaela Stampfer-Kountchev,Martin Sawires,Christoph Scherfler,Sylvia Boesch,Joerg Mueller,Vasiliki Koukouni,Niall Quinn,Maria Teresa Pellecchia,Paolo Barone,Nicole Schimke,Richard Dodel,Wolfgang H. Oertel,Erik Dupont,Karen Østergaard,C. Daniels,Günther Deuschl,Tanya Gurevich,Nir Giladi,Miguel Coelho,Cristina Sampaio,Christer Nilsson,Håkan Widner,Francesca Del Sorbo,Alberto Albanese,Adriana Cardozo,Eduardo Tolosa,Michael Abele,Thomas Klockgether,Christoph Kamm,Thomas Gasser,Ruth Djaldetti,Carlo Colosimo,Giuseppe Meco,Anette Schrag,Werner Poewe,Gregor K. Wenning +38 more
TL;DR: A combination of two out of six red flag categories as additional diagnostic criteria for probable MSA‐P is proposed and 76.5% of them would have been correctly diagnosed as probable Msa‐P 15.9 months earlier than with the Consensus criteria alone.