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Britton Zuccarelli

Showing results (1-10 of 7) with videos related to

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Neurology. Clinical Practice|February 15, 2018
Reducing after-hours prescription refill requestsBritton Zuccarelli, Keith A Coffman
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 12, 2016
Hemiballismus as a complication of an intratumoral chemotherapy catheterBritton Zuccarelli, Brian Aalbers, Paul Grabb
BMC Medical Genetics|November 4, 2017
Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related diseaseIsabelle Thiffault, Britton Zuccarelli, Holly Welsh, et al.
Journal of Inherited Metabolic Disease|December 15, 2017
An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variantsAna Pop, Monique Williams, Eduard A Struys, et al.
Science Translational Medicine|December 5, 2014
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disordersSarah E Soden, Carol J Saunders, Laurel K Willig, et al.
American Journal of Human Genetics|January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctionJoery den Hoed, Elke de Boer, Norine Voisin, et al.
JAMA Neurology|October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical PracticeDianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Neurology. Clinical Practice|February 15, 2018
Reducing after-hours prescription refill requestsBritton Zuccarelli, Keith A Coffman
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 12, 2016
Hemiballismus as a complication of an intratumoral chemotherapy catheterBritton Zuccarelli, Brian Aalbers, Paul Grabb
BMC Medical Genetics|November 4, 2017
Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related diseaseIsabelle Thiffault, Britton Zuccarelli, Holly Welsh, et al.
Journal of Inherited Metabolic Disease|December 15, 2017
An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variantsAna Pop, Monique Williams, Eduard A Struys, et al.
Science Translational Medicine|December 5, 2014
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disordersSarah E Soden, Carol J Saunders, Laurel K Willig, et al.
American Journal of Human Genetics|January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctionJoery den Hoed, Elke de Boer, Norine Voisin, et al.
JAMA Neurology|October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical PracticeDianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
Pageof 1