Brent Fogel

Summary

Affiliation: University of California
Country: USA

Publications

  1. pmc RBFOX1 regulates both splicing and transcriptional networks in human neuronal development
    Brent L Fogel
    Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Mol Genet 21:4171-86. 2012
  2. pmc Childhood cerebellar ataxia
    Brent L Fogel
    Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA
    J Child Neurol 27:1138-45. 2012
  3. pmc Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia
    Brent L Fogel
    Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California 90095, USA
    Mov Disord 27:442-6. 2012
  4. pmc Aberrant splicing of the senataxin gene in a patient with ataxia with oculomotor apraxia type 2
    Brent L Fogel
    Department of Neurology, UCLA Program in Neurogenetics, David Geffen School of Medicine, University of California at Los Angeles, 710 Westwood Plaza, Los Angeles, CA 90095, USA
    Cerebellum 8:448-53. 2009
  5. doi request reprint A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes
    Brent L Fogel
    Department of Neurology, University of California at Los Angeles, David Geffen School of Medicine, Los Angeles, CA 90095, USA
    Neurogenetics 9:215-8. 2008
  6. ncbi request reprint Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2
    Brent L Fogel
    Department of Neurology, University of California at Los Angeles, 710 Westwood Plaza, Los Angeles, CA 90095, USA
    Neurology 67:2083-4. 2006
  7. ncbi request reprint Magnetic resonance imaging abnormalities in the corpus callosum of a patient with neuropsychiatric lupus
    Brent Fogel
    Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA
    Neurologist 12:271-3. 2006
  8. ncbi request reprint Creutzfeldt-Jakob disease presenting with alien limb sign
    Brent Fogel
    Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA
    Mov Disord 21:1040-2. 2006
  9. ncbi request reprint Clinical features and molecular genetics of autosomal recessive cerebellar ataxias
    Brent L Fogel
    Department of Neurology, David Geffen School of Medicine at UCLA, University of California at Los Angeles, 90095, USA
    Lancet Neurol 6:245-57. 2007
  10. ncbi request reprint An approach to the patient with late-onset cerebellar ataxia
    Brent L Fogel
    Department of Neurology, University of California, Los Angeles, CA 90095, USA
    Nat Clin Pract Neurol 2:629-35; quiz 1 p following 635. 2006

Detail Information

Publications10

  1. pmc RBFOX1 regulates both splicing and transcriptional networks in human neuronal development
    Brent L Fogel
    Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Mol Genet 21:4171-86. 2012
    ....
  2. pmc Childhood cerebellar ataxia
    Brent L Fogel
    Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA
    J Child Neurol 27:1138-45. 2012
    ..Systematic investigation is recommended for efficient diagnosis. In this review, we outline common etiologies and describe a comprehensive approach to the evaluation of both acquired and genetic cerebellar ataxia in children...
  3. pmc Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia
    Brent L Fogel
    Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California 90095, USA
    Mov Disord 27:442-6. 2012
    ..Rare genetic ataxias, reported only in specific populations or families, may contribute to a percentage of sporadic ataxia...
  4. pmc Aberrant splicing of the senataxin gene in a patient with ataxia with oculomotor apraxia type 2
    Brent L Fogel
    Department of Neurology, UCLA Program in Neurogenetics, David Geffen School of Medicine, University of California at Los Angeles, 710 Westwood Plaza, Los Angeles, CA 90095, USA
    Cerebellum 8:448-53. 2009
    ..RNA processing mutations expand the growing complexity of pathogenic senataxin mutations...
  5. doi request reprint A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes
    Brent L Fogel
    Department of Neurology, University of California at Los Angeles, David Geffen School of Medicine, Los Angeles, CA 90095, USA
    Neurogenetics 9:215-8. 2008
    ..Given the impact of this result on the heritability of the two disorders within the family, this case illustrates the significance of performing detailed molecular analysis in patients with multiple genetic disorders...
  6. ncbi request reprint Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2
    Brent L Fogel
    Department of Neurology, University of California at Los Angeles, 710 Westwood Plaza, Los Angeles, CA 90095, USA
    Neurology 67:2083-4. 2006
  7. ncbi request reprint Magnetic resonance imaging abnormalities in the corpus callosum of a patient with neuropsychiatric lupus
    Brent Fogel
    Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA
    Neurologist 12:271-3. 2006
    ..Currently, there are no consensus neuroimaging findings associated with neuropsychiatric SLE...
  8. ncbi request reprint Creutzfeldt-Jakob disease presenting with alien limb sign
    Brent Fogel
    Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA
    Mov Disord 21:1040-2. 2006
    ..Here we report the unusual case of a patient who presented with left alien limb sign without overt cognitive impairment and was ultimately diagnosed with pathologically confirmed Creutzfeldt-Jakob disease...
  9. ncbi request reprint Clinical features and molecular genetics of autosomal recessive cerebellar ataxias
    Brent L Fogel
    Department of Neurology, David Geffen School of Medicine at UCLA, University of California at Los Angeles, 90095, USA
    Lancet Neurol 6:245-57. 2007
    ..In this Review, we discuss the clinical characteristics and molecular genetics of the more common autosomal recessive ataxias and provide a framework for assessment and differential diagnosis of patients with these disorders...
  10. ncbi request reprint An approach to the patient with late-onset cerebellar ataxia
    Brent L Fogel
    Department of Neurology, University of California, Los Angeles, CA 90095, USA
    Nat Clin Pract Neurol 2:629-35; quiz 1 p following 635. 2006
    ..The patient then underwent multiple evaluations for an underlying paraneoplastic process, all of which were negative, but his symptoms progressed and he remained undiagnosed for several years...