Dr. Brent Linden Fogel M.D
Neurologist | Neurology
300 Medical Plaza Suite B200 Los Angeles CA, 90095About
Dr. Brent Fogel is a distinguished Neurologist in Los Angeles, CA. Dr. Fogel 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. Fogel employs advanced techniques and personalized treatment plans to improve patient outcomes. As a neurologist, Dr. Fogel is committed to staying abreast of the latest developments in neurological research and therapies.
Education and Training
Med College Of Wisconsin 1998
Board Certification
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Trace contamination following reuse of anion-exchange DNA purification resins.
- A cellular protein, hnRNP H, binds to the negative regulator of splicing element from Rous sarcoma virus.
- An approach to the patient with late-onset cerebellar ataxia.
- Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2.
- Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.
- A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes.
- Aberrant splicing of the senataxin gene in a patient with ataxia with oculomotor
- New-onset psychosis in a patient with spinocerebellar ataxia type 10.
- Childhood cerebellar ataxia.
- Interpretation of genetic testing: variants of unknown significance.
- A family with spinocerebellar ataxia type 5 found to have a novel missense mutation within a SPTBN2 spectrin repeat.
- Clinical neurogenetics: autosomal dominant spinocerebellar ataxia.
- Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder.
- Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
- A new model to study neurodegeneration in ataxia oculomotor apraxia type 2.
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