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Publications by Maria Anvret

A Rare Truncating Mutation in ADH1C (G78Stop) Shows Significant Association With Parkinson Disease in a Large International Sample

Archives of Neurology

English

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Lafora Disease in a Malaysian With a Rare Mutation in the EPM2A Gene

Seizure : the journal of the British Epilepsy Association

English

Cold Agglutinin Disease in Fibrolamellar Hepatocellular Carcinoma: A Rare Association With a Rare Cancer Variant

Annals of Saudi Medicine

English

Corrigendum: Sarcoidosis Is Associated With a Truncating Splice Site Mutation in the Gene BTNL2

Nature Genetics

English

Variant Alzheimer Disease With Spastic Paraparesis: A Rare Presenilin-1 Mutation

Canadian Journal of Neurological Sciences

English

Rare Genetic Creutzfeldt-Jakob Disease With E196A Mutation: A Case Report

Molecular Neuroscience

Infectious Diseases

English

Parkinson Disease in a Patient With Multiple Co-Morbidities

Kansas Journal of Medicine

English

Transcranial Sonography and Functional Imaging in Glucocerebrosidase Mutation Parkinson Disease

Parkinsonism and Related Disorders

English

A Novel Homozygous Truncating Mutation in LAMB2 Gene in a Chinese Uyghur Patient With Severe Phenotype Pierson Syndrome

Frontiers in Medicine

English

Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease

Archives of Neurology

English