Area of research
Neurology · Molecular Biology
Research interest
Research interests include Prion Diseases and Protein Misfolding, Neurological diseases and metabolism, Autoimmune Neurological Disorders and Treatments, and Genetic Neurodegenerative Diseases.
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3
Skin Biopsy Detection of Phosphorylated α-Synuclein in Patients With Synucleinopathies
The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias
SARA captures disparate progression and responsiveness in spinocerebellar ataxias
Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias
Altered Iron and Microstructure in Huntington's Disease Subcortical Nuclei: Insight From 7T MRI
Autoimmune Encephalitis Misdiagnosis in Adults
Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy
The S-Factor, a New Measure of Disease Severity in Spinocerebellar Ataxia: Findings and Implications
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Seizure-related 6 homolog like 2 autoimmunity
Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD
Anti-gamma-aminobutyric acid receptor type A encephalitis: a review
The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3
Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6
Baseline neuropsychological profiles in prion disease predict survival time
Dementia assessment and management in primary care settings: a survey of current provider practices in the United States
Association of Blood and Cerebrospinal Fluid Tau Level and Other Biomarkers With Survival Time in Sporadic Creutzfeldt-Jakob Disease
Age at onset in genetic prion disease and the design of preventive clinical trials
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders
Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development
Distinct HLA associations of LGI1 and CASPR2-antibody diseases
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients
The importance of early immunotherapy in patients with faciobrachial dystonic seizures
MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study
Dystonia and ataxia progression in spinocerebellar ataxias