Assistant Professor, Neurology, UCLA School of Medicine
Neurology
Dr. Brent L. Fogel, MD
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Dr. Brent L. Fogel works in the field of Neurology. He went to medical school at Medical College of Wisconsin. Medical College of Wisconsin is ranked 54/62 in Research/PrimaryCare. Brent L. Fogel, MD is a published doctor and has 26 publications published. The lastest was: 'Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?' He is registered with Medicare and accepts Medicare payments.
Publications
- Do mutations in the murine Ataxia gene TRPC3 cause cerebellar Ataxia in humans?
- Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders.
- Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar Ataxia.
- The neurogenetics of atypical parkinsonian disorders.
- Mutation of Senataxin Alters Disease-Specific Transcriptional Networks in Patients with Ataxia with Oculomotor Apraxia Type 2.
- Utilization of genetic testing prior to subspecialist referral for cerebellar Ataxia.
- Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
- Mutations in PDYN are not responsible for multiple system atrophy.
- C9ORF72 expansion is not a significant cause of sporadic spinocerebellar Ataxia.
- RBFOX1 regulates both splicing and transcriptional networks in human neuronal development.
- Childhood cerebellar Ataxia.
- A Family with Spinocerebellar Ataxia Type 5 Found to Have a Novel Missense Mutation within a SPTBN2 Spectrin Repeat.
- New-onset psychosis in a patient with spinocerebellar Ataxia type 10.
- Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia.
- Aberrant splicing of the senataxin gene in a patient with Ataxia with oculomotor apraxia type 2.
- A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes.
- Novel mutations in the senataxin DNA/RNA helicase domain in Ataxia with oculomotor apraxia 2.
- Orchestration of Neurodevelopmental Programs by RBFOX1: Implications for Autism Spectrum Disorder.
- Clinical features and molecular genetics of autosomal recessive cerebellar Ataxias.
- An approach to the patient with late-onset cerebellar Ataxia.
- 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.
- Efficient polyadenylation of Rous sarcoma virus RNA requires the negative regulator of splicing element.
- Creutzfeldt-Jakob Disease presenting with alien limb sign.
- Magnetic resonance imaging abnormalities in the corpus callosum of a patient with neuropsychiatric lupus.
Schools
Medical College of Wisconsin
Procedures Preformed
- EEG (Electroencephalogram)
Conditions Treated
- Ataxia
- Dystonia
- Gait Abnormality
- Parkinson's Disease
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Doctors Specialties
- Neurology
Accepted Insurances
Education
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UCLA Medical Center -
McGaw Medical Center of Northwestern University -
Medical College of Wisconsin
Hospital
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Ronald Reagan UCLA Medical Center
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1629289178 |
| Last Name Of The Provider | FOGEL |
| First Name Of The Provider | BRENT |
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