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Brent L Fogel

Showing results (1-10 of 83) with videos related to

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Developmental Medicine and Child Neurology|October 10, 2024
Intersecting genomics and imaging for precision care in prenatal counselingBrent L Fogel
Annals of Neurology|June 17, 2018
Collaborative science unites researchers and a novel spastic ataxia geneBrent L Fogel
Handbook of Clinical Neurology|January 13, 2018
Genetic and genomic testing for neurologic disease in clinical practiceBrent L Fogel
Journal of Child Neurology|July 6, 2012
Childhood cerebellar ataxiaBrent L Fogel
Handbook of Clinical Neurology|January 13, 2018
Autosomal-recessive cerebellar ataxiasBrent L Fogel
Continuum (Minneapolis, Minn.)|July 20, 2012
Interpretation of genetic testing: variants of unknown significanceBrent L Fogel
The Lancet. Neurology|February 17, 2007
Clinical features and molecular genetics of autosomal recessive cerebellar ataxiasBrent L Fogel, Susan Perlman
The American Journal of Psychiatry|December 24, 2011
New-onset psychosis in a patient with spinocerebellar ataxia type 10Eric Wexler, Brent L Fogel
Neurology|December 13, 2006
Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2Brent L Fogel, Susan Perlman
Cerebellum & Ataxias|November 1, 2018
Successful treatment of a genetic childhood ataxia due to riboflavin transporter deficiencyJudy Fan, Brent L Fogel
Pageof 9

Showing results (1-10 of 83) with videos related to

Sort By:
Pageof 9
Developmental Medicine and Child Neurology|October 10, 2024
Intersecting genomics and imaging for precision care in prenatal counselingBrent L Fogel
Annals of Neurology|June 17, 2018
Collaborative science unites researchers and a novel spastic ataxia geneBrent L Fogel
Handbook of Clinical Neurology|January 13, 2018
Genetic and genomic testing for neurologic disease in clinical practiceBrent L Fogel
Journal of Child Neurology|July 6, 2012
Childhood cerebellar ataxiaBrent L Fogel
Handbook of Clinical Neurology|January 13, 2018
Autosomal-recessive cerebellar ataxiasBrent L Fogel
Continuum (Minneapolis, Minn.)|July 20, 2012
Interpretation of genetic testing: variants of unknown significanceBrent L Fogel
The Lancet. Neurology|February 17, 2007
Clinical features and molecular genetics of autosomal recessive cerebellar ataxiasBrent L Fogel, Susan Perlman
The American Journal of Psychiatry|December 24, 2011
New-onset psychosis in a patient with spinocerebellar ataxia type 10Eric Wexler, Brent L Fogel
Neurology|December 13, 2006
Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2Brent L Fogel, Susan Perlman
Cerebellum & Ataxias|November 1, 2018
Successful treatment of a genetic childhood ataxia due to riboflavin transporter deficiencyJudy Fan, Brent L Fogel
Pageof 9