Dr. Cyrus Parse Zabetian MD
Neurologist | Neurology
1660 S Columbian Way Grecc (s-182), Va Pu Seattle WA, 98108About
Dr. Cyrus Zabetian is a distinguished Neurologist in Seattle, WA. Dr. Zabetian specializes in diagnosing, treating, and managing disorders of the brain and nervous system. With expertise in handling complex conditions like epilepsy, multiple sclerosis, and migraines, Dr. Zabetian employs advanced techniques and personalized treatment plans to improve patient outcomes. As a neurologist, Dr. Zabetian is committed to staying abreast of the latest developments in neurological research and therapies.
Education and Training
University of Miami Leonard M. Miller School of Medicine 1994
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Variations in the dopamine beta-hydroxylase gene are not associated with the autonomic disorders, pure autonomic failure, or multiple system atrophy.
- Sigma receptors are associated with cortical limbic areas in the primate brain.
- Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology.
- Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation.
- Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease.
- Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
- Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.
- DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease.
- Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease.
- Exploring gene-environment interactions in Parkinson's disease.
- Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
- Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
- Genetic association between alpha-synuclein and idiopathic Parkinson's disease.
- Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
- LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay.
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