Overview
Sara Dehbashi is a Neurologist in Washington, Washington, D.c.. Dr. Dehbashi is rated as an Advanced provider by MediFind in the treatment of Infantile Axonal Neuropathy. Her top areas of expertise are Peripheral Neuropathy, Myasthenia Gravis, Congenital Insensitivity to Pain with Anhidrosis, and Infantile Axonal Neuropathy.
Her clinical research consists of co-authoring 5 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- HMO
- PPO
- EPO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- MANAGED MEDICAID PLAN
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
3800 Reservoir Rd Nw, Washington, DC 20007
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Neurological Medicine, P.A.
Maciej Poltorak is a Neurologist in Greenbelt, Maryland. Dr. Poltorak is rated as a Distinguished provider by MediFind in the treatment of Infantile Axonal Neuropathy. His top areas of expertise are Congenital Insensitivity to Pain with Anhidrosis, Hereditary Sensory and Autonomic Neuropathy Type 2, Infantile Axonal Neuropathy, and Partial Familial Epilepsy. Dr. Poltorak is currently accepting new patients.
Johns Hopkins University
Ahmet Hoke is a Neurologist in Baltimore, Maryland. Dr. Hoke is rated as a Distinguished provider by MediFind in the treatment of Infantile Axonal Neuropathy. His top areas of expertise are Wallerian Degeneration, Peripheral Neuropathy, Tomaculous Neuropathy, Hereditary Sensory and Autonomic Neuropathy Type 2, and Prostatectomy. Dr. Hoke is currently accepting new patients.
Neurological Medicine, P.A.
Syed Asad is a Neurologist in Greenbelt, Maryland. Dr. Asad is rated as a Distinguished provider by MediFind in the treatment of Infantile Axonal Neuropathy. His top areas of expertise are Cerebellar Degeneration, Partial Familial Epilepsy, Partial Seizure, and Memory Loss. Dr. Asad is currently accepting new patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Congenital Insensitivity to Pain with Anhidrosis
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Infantile Axonal NeuropathyDr. Dehbashi isAdvanced. Learn about Infantile Axonal Neuropathy.
- Myasthenia GravisDr. Dehbashi isAdvanced. Learn about Myasthenia Gravis.
- Peripheral NeuropathyDr. Dehbashi isAdvanced. Learn about Peripheral Neuropathy.
- Experienced
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Andermann SyndromeDr. Dehbashi isExperienced. Learn about Andermann Syndrome.
- Brachial PlexopathyDr. Dehbashi isExperienced. Learn about Brachial Plexopathy.
- Charcot-Marie-Tooth DiseaseDr. Dehbashi isExperienced. Learn about Charcot-Marie-Tooth Disease.
- Chromosome 11 Uniparental DisomyDr. Dehbashi isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 2 Uniparental DisomyDr. Dehbashi isExperienced. Learn about Chromosome 2 Uniparental Disomy.