Mathieu Anheim

International Space University — France

Neuroscience · Life Sciences

59h-index15.9kcitations374works9.22yr avg
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Research Topics

Genetic Neurodegenerative Diseases(148), Mitochondrial Function and Pathology(105), Parkinson's Disease Mechanisms and Treatments(97), Neurological disorders and treatments(91), Neurological diseases and metabolism(51)

Publications369 total

Effect on Dyskinesia of the Early Combination of Amantadine to Levodopa‐Therapy in Parkinson's Disease: A Randomized, Placebo‐Controlled Study ( <scp>PREMANDYSK</scp> )
Movement Disorders·2025· 1 citedOpen Access
Author Correction: Classification of GBA1 variants and their impact on Parkinson’s disease: an in silico score analysis
npj Parkinson s Disease·2025Open Access
Motor complications and postural abnormalities interplay in Parkinson's disease
Parkinsonism & Related Disorders·2025
<scp> <i>RRP12</i> </scp> Variants Are Associated With Autosomal Recessive Brain Calcifications
Movement Disorders·2025· 1 citedOpen Access
Type and position of repeat interruptions as determinants of disease severity and expansion size in Friedreich ataxia
Genetics in Medicine·2025· 1 cited
Progress and challenges in sporadic late-onset cerebellar ataxias
Nature Reviews Neurology·2025· 1 cited
A clinical and genotype-phenotype analysis of MACF1 variants
The American Journal of Human Genetics·2025· 1 citedOpen Access
Classification of GBA1 variants and their impact on Parkinson’s disease: an in silico score analysis
npj Parkinson s Disease·2025· 3 citedOpen Access
The Two Faces of Pediatric <scp>SCA2</scp>
European Journal of Neurology·2025· 1 citedOpen Access
Neuropsychiatric fluctuations in Parkinson's disease: A French multicenter study of the NFS psychometric properties
Parkinsonism & Related Disorders·2025· 1 citedOpen Access
Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series
Journal of Neurology·2025· 2 cited
The Spectrum of Neurologic Phenotypes Associated With <scp><i>NUS1</i></scp> Pathogenic Variants: A Comprehensive Case Series
Annals of Neurology·2025· 5 citedOpen Access
Exploring the link between personality dimensions and non-motor fluctuations in Parkinson's disease
Journal of Parkinson s Disease·2025Open Access
Neuropathy in <scp>GAA</scp>‐<scp>FGF14</scp> Late‐Onset Cerebellar Ataxia (<scp>SCA27B</scp>): Prevalence and Characteristics
European Journal of Neurology·2025· 5 citedOpen Access
<scp> <i>ADCY5</i> </scp> ‐Mosaic Variants: A Diagnosis Not to Be Missed
Movement Disorders Clinical Practice·2025· 1 citedOpen Access
Managing Aminotransferase Elevations in Patients with Friedreich Ataxia Treated with Omaveloxolone: A Review and Expert Opinion on Use Considerations
Neurology and Therapy·2025· 7 citedOpen Access
French guidelines for the diagnosis and management of pure hereditary spastic paraplegia
Revue Neurologique·2025· 3 citedOpen Access
Trigeminal Tract Abnormality Leading to Leukodystrophy With Brainstem and Spinal Cord Involvement and High Lactate Diagnosis
Neurology·2025
Parkinson's Disease, Speech and Neurosurgery
Brain and Behavior·2025· 1 citedOpen Access
Improvement of apathy in early Parkinson’s disease
npj Parkinson s Disease·2025· 1 citedOpen Access
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Frequent Co-authors

Alexandra Dürr(29), Christine Tranchant(26), Alexis Brice(25), Marie Vidailhet(21), Michel Kœnig(15), Suzanne Lesage(11), François Tison(10), Jean‐Christophe Corvol(10), Pierre Pollak(10), Giovanni Stévanin(10), Didier Hannequin(10), Cyril Goizet(10), Perrine Charles(10), Ebba Lohmann(8), François Viallet(8), A. Destée(7), Philippe Damier(7), Nathalie Drouot(7), David Maltête(7), Emmanuel Roze(7)