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Fingerprint Dive into the research topics where Caterina Mariotti is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Medicine & Life Sciences

Spinocerebellar Ataxias
Ataxia
Huntington Disease
Friedreich Ataxia
Mutation
Cerebellar Ataxia
Genes
Phenotype
Mitochondrial DNA
Age of Onset
CADASIL
Atrophic Muscular Disorders
Alleles
Neurodegenerative Diseases
Disease Progression
Cerebellar Diseases
Genotype
Oculomotor Muscles
Point Mutation
Eye Movements
Spinocerebellar Degenerations
Cerebellum
Eye Abnormalities
Molecular Biology
Paraplegia
Genetic Testing
Muscles
Atrophy
Guidelines
Brain
Randomized Controlled Trials
Genetic Association Studies
Parkinson Disease
Cohort Studies
Corpus Striatum
Cardiomyopathies
Muscular Atrophy
Mitochondrial Diseases
Saccades
Alexander Disease
Ophthalmoplegia
Dysarthria
Longitudinal Studies
coenzyme Q10
Placebos
Vitamin E Deficiency
Electron Transport
Gait
Dystonia
Biomarkers