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Publications by Davide Pareyson

Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage

American Journal of Human Genetics

English

Natural History of Charcot-Marie-Tooth Disease During Childhood

Annals of Neurology

English

An Essential Role of MAG in Mediating Axon–myelin Attachment in Charcot–Marie–Tooth 1A Disease

Neurobiology of Disease

English

The Italian Neuromuscular Registry: A Coordinated Platform Where Patient Organizations and Clinicians Collaborate for Data Collection and Multiple Usage

Orphanet Journal of Rare Diseases

English

SETX Mutations Are a Frequent Genetic Cause of Juvenile and Adult Onset Cerebellar Ataxia With Neuropathy and Elevated Serum Alpha-Fetoprotein

Orphanet Journal of Rare Diseases

English

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study

Journal of Neuromuscular Diseases

English