The Pattern and Stages of Atrophy in Spinocerebellar Ataxia Type 2: Volumetrics from <scp>ENIGMA</scp>‐Ataxia

The magnitude and pattern of brain atrophy evolve over the course of SCA2, with widespread, nonuniform involvement across the brainstem, cerebellar tracts, and cerebellar cortex; and late involvement of the cerebral cortex and striatum. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Journal
Movement Disorders
Published
2025-02-10
DOI
https://doi.org/10.1002/mds.30143
Citations
1
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.91

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article

The Pattern and Stages of Atrophy in Spinocerebellar Ataxia Type 2: Volumetrics from ENIGMA‐Ataxia

Imis Dogan, Sophia Göricke, Anna Nigri, Wolfgang Nachbauer et al.
1 citations
Movement Disorders
Genetic Neurodegenerative Diseases
0.91
article

The Pattern and Stages of Atrophy in Spinocerebellar Ataxia Type 2: Volumetrics from ENIGMA‐Ataxia

Imis Dogan, Sophia Göricke, Anna Nigri, Wolfgang Nachbauer, Lorenzo Nanetti, Sophia I. Thomopoulos, Alexandra Dürr, Francesco Saccà, Matthis Synofzik, Sandro Romanzetti, Marina Grisoli, Carlos R. Hernandez‐Castillo, Jason W. Robertson, Chiadi U. Onyike, Fanny Mochel, Caterina Mariotti, Kathrin Reetz, Isaac Adanyeguh, Sergio Eiji Ono, Benjamin Bender, Hélio Afonso Ghizoni Teive, Sylvia Boesch, Ian H. Harding, Dagmar Timmann, Mario Mascalchi, Jerry L. Prince, Stefano Diciotti, Shuo Han, Sirio Cocozza, Juan Fernández-Ruíz, Léo Coutinho, Andreas Deistung, Chiara Marzi, Arturo Brunetti, Paul M. Thompson, Sarah H. Ying
article en
1 citations

Abstract

The magnitude and pattern of brain atrophy evolve over the course of SCA2, with widespread, nonuniform involvement across the brainstem, cerebellar tracts, and cerebellar cortex; and late involvement of the cerebral cortex and striatum. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Movement DisordersVol. 40(4)
University of Southern California (US), Centre National de la Recherche Scientifique (FR), Dalhousie University (CA), Innsbruck Medical University (AT), Johns Hopkins University (US), Inserm (FR), Universität Innsbruck (AT), QIMR Berghofer Medical Research Institute (AU), Marconi University (IT), German Center for Neurodegenerative Diseases (DE), Sorbonne Université (FR), Centrus Diagnósticos por Imagem (BR), Laboratori Guglielmo Marconi (Italy) (IT), Essen University Hospital (DE), Pitié-Salpêtrière Hospital (FR), Jülich Aachen Research Alliance (DE), Hospital de Clínicas Universidade Federal do Paraná (BR), Hertie Institute for Clinical Brain Research (DE), University Hospital in Halle (DE), Institut du Cerveau (FR), Fondazione IRCCS Istituto Neurologico Carlo Besta (IT), University of Florence (IT), Universidade Federal do Paraná (BR), Monash University (AU), University of Duisburg-Essen (DE), University of Naples Federico II (IT), RWTH Aachen University (DE), Universidad Nacional Autónoma de México (MX), University of Bologna (IT)
National Science Foundation, National Ataxia Foundation, Johns Hopkins University, Deutsche Forschungsgemeinschaft, Canada Research Chairs, Bundesministerium für Bildung und Forschung, Consejo Nacional de Ciencia y Tecnología, Ministero della Salute, National Institutes of Health, Natural Sciences and Engineering Research Council of Canada, Medical Research Council, National Health and Medical Research Council, Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México, National Institute of Neurological Disorders and Stroke, National Center for Advancing Translational Sciences
Good health and well-being
Openalex Percentile: Top 31%
Genetic Neurodegenerative Diseases
0.91
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