Claudia Stendel

German Center for Neurodegenerative Diseases — Germany

Neuroscience · Life Sciences

24h-index2.7kcitations51works2.32yr avg
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Research Topics

Genetic Neurodegenerative Diseases(19), Mitochondrial Function and Pathology(18), Hereditary Neurological Disorders(17), Parkinson's Disease Mechanisms and Treatments(6), Metabolism and Genetic Disorders(5)

Publications51 total

Analysis of a Modified Version of the Inventory of Non‐Ataxia Signs Over 12 Years in Patients with Friedreich's Ataxia in the <scp>EFACTS</scp> Study
Movement Disorders·2025Open Access
Longitudinal analysis of anthropometric measures over 5 years in patients with Friedreich ataxia in the <scp>EFACTS</scp> natural history study
European Journal of Neurology·2025· 1 citedOpen Access
Health-Related Quality of Life in Patients with Friedreich Ataxia Using Mobility Assistive Technologies: Limited Fit of the EQ-5D-3L Mobility Dimension
Neurology and Therapy·2024Open Access
Phase 2b program with sonlicromanol in patients with mitochondrial disease due to m.3243A&amp;gt;G mutation
Brain·2024· 8 citedOpen Access
Clinical, Imaging, Genetic, and Disease Course Characteristics in Patients With GM2 Gangliosidosis
Neurology·2023· 7 citedOpen Access
Longitudinal changes of <scp>SARA</scp> scale in Friedreich ataxia: Strong influence of baseline score and age at onset
Annals of Clinical and Translational Neurology·2023· 6 citedOpen Access
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias
The American Journal of Human Genetics·2023· 28 citedOpen Access
Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult‐Onset Degenerative Ataxia
Movement Disorders·2023· 14 citedOpen Access
Prediction of the disease course in Friedreich ataxia
Scientific Reports·2022· 8 citedOpen Access
Mitochondriale Erkrankungen – Ein Update zu Klinik, Diagnostik und Therapie
Neurologie up2date·2022· 2 cited
Cerebellar Bottom of Fissure Hyperintensities in <scp><i>MT‐ATP6</i></scp>‐Associated Ataxia
Annals of Neurology·2022· 1 citedOpen Access
Mast Syndrome Outside the Amish Community: SPG21 in Europe
Frontiers in Neurology·2022· 6 citedOpen Access
Safety and Efficacy of Acetyl-DL-Leucine in Certain Types of Cerebellar Ataxia
JAMA Network Open·2021· 35 citedOpen Access
Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers’ Lives
Brain Sciences·2021· 59 citedOpen Access
Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study
The Lancet Neurology·2021· 89 cited
Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia
International Journal of Molecular Sciences·2020· 20 citedOpen Access
Delineating <i>MT-ATP6</i> -associated disease
Neurology Genetics·2020· 104 citedOpen Access
Progression Characteristics in Friedreich's Ataxia: A 4-Year Observational Study
SSRN Electronic Journal·2020Open Access
Gillespie's Syndrome with Minor Cerebellar Involvement and No Intellectual Disability Associated with a Novel ITPR1 Mutation: Report of a Case and Literature Review
Neuropediatrics·2019· 11 cited
Klinisches und genetisches Spektrum MT-ATP6- und MT-ATP8-assoziierter Erkrankungen
Nervenheilkunde·2019
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Frequent Co-authors

Thomas Klopstock(27), Jan Senderek(18), Lüdger Schöls(18), Sylvia Boesch(13), Wolfgang Nachbauer(13), Thomas Klockgether(12), Ilaria Giordano(12), Caterina Mariotti(11), Joachim Weis(10), Alexandra Dürr(10), Claire Ewenczyk(10), Lorenzo Nanetti(10), Klaus Zerres(9), Kathrin Reetz(9), Paola Giunti(9), Francisco Javier Rodríguez de Rivera Garrido(9), Jörg B. Schulz(9), Matthis Synofzik(9), Carsten Bergmann(8), Imis Dogan(8)