The Medication Patterns of Spinocerebellar Ataxia Type 3 Mutation Carriers Enrolled in the ESMI Cohort

This is the first study to explore medication usage patterns in SCA3 mutation carriers. Our study provides a comprehensive overview of the medications administered in SCA3 and underscores the importance of collaborative efforts toward achieving standardized clinical practices in the management of this disease.

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Publication Details

Journal
CNS Drugs
Published
2025-10-17
DOI
https://doi.org/10.1007/s40263-025-01237-w
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

The Medication Patterns of Spinocerebellar Ataxia Type 3 Mutation Carriers Enrolled in the ESMI Cohort

Héctor García‐Moreno, Paula Pires, João Vasconcelos, Bart P.C. van de Warrenburg et al.
CNS Drugs
Genetic Neurodegenerative Diseases
article

The Medication Patterns of Spinocerebellar Ataxia Type 3 Mutation Carriers Enrolled in the ESMI Cohort

Héctor García‐Moreno, Paula Pires, João Vasconcelos, Bart P.C. van de Warrenburg, Manuela Lima, Jon Infante, Pedro Lopes, Mafalda Raposo, Luís Pereira de Almeida, Ana Paula Rosa, João Durães, Magda M. Santana, Kathrin Reetz, Cristina Januário, Inês Cunha, Pedro Coelho, Cristina Gonzalez‐Robles, Ana F. Ferreira, Paola Giunti, Jennifer Faber, Dagmar Timmann, Laetitia S. Gaspar, Heike Jacobi, Luís Teves, Friedrich Erdlenbruch, Andreas Gustafsson Thieme, Ludger J. Schöls, João Lemos, Lukas Beichert, Carlos González, Patrick Silva, Joana Ribeiro, Jeannette Hübener‐Schmid, Bárbara Oliveiros, Thomas Klockgether, Jeroen J. de Vries, Teresa Kay, M Costa
article en

Abstract

This is the first study to explore medication usage patterns in SCA3 mutation carriers. Our study provides a comprehensive overview of the medications administered in SCA3 and underscores the importance of collaborative efforts toward achieving standardized clinical practices in the management of this disease.

CNS DrugsVol. 40(2)
Universidade dos Açores (PT), University Medical Center Groningen (NL), Radboud University Nijmegen (NL), Universidade do Porto (PT), Heidelberg University (DE), University Hospital Bonn (DE), German Center for Neurodegenerative Diseases (DE), Hospitais da Universidade de Coimbra (PT), University Hospital Heidelberg (DE), Radboud University Medical Center (NL), Biomedical Research Networking Center on Neurodegenerative Diseases (ES), Instituto de Investigación Marqués de Valdecilla (ES), Gene PreDiT (Portugal) (PT), Centro de Investigación Biomédica en Red (ES), Universitätsklinikum Aachen (DE), Hertie Institute for Clinical Brain Research (DE), National Hospital for Neurology and Neurosurgery (GB), i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto (PT), Institute for Biotechnology and Bioengineering (PT), University College London (GB), University of Coimbra (PT), University of Tübingen (DE), RWTH Aachen University (DE)
Friedreich's Ataxia Research Alliance, National Ataxia Foundation, Fundo Regional para a Ciência e Tecnologia, EU Joint Programme – Neurodegenerative Disease Research, European Federation of Pharmaceutical Industries and Associations, National Institute for Health and Care Research, University College London, European Commission, Deutsche Forschungsgemeinschaft, ZonMw, Bundesministerium für Bildung und Forschung, Else Kröner-Fresenius-Stiftung, RWTH Aachen University, Hersenstichting, University College London Hospitals NHS Foundation Trust, Programa Operacional Regional do Centro, HORIZON EUROPE Framework Programme, Medical Research Council, Fundação para a Ciência e a Tecnologia, European Regional Development Fund, Medizinische Fakultät, RWTH Aachen University
Openalex Percentile: Top 68%
Genetic Neurodegenerative Diseases
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