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Neurology. Clinical Practice
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February 15, 2018
Reducing after-hours prescription refill requests
Britton 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 catheter
Britton Zuccarelli, Brian Aalbers, Paul Grabb
BMC Medical Genetics
|
November 4, 2017
Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease
Isabelle 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 variants
Ana 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 disorders
Sarah 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 dysfunction
Joery 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 Practice
Dianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Neurology. Clinical Practice
|
February 15, 2018
Reducing after-hours prescription refill requests
Britton 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 catheter
Britton Zuccarelli, Brian Aalbers, Paul Grabb
BMC Medical Genetics
|
November 4, 2017
Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease
Isabelle 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 variants
Ana 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 disorders
Sarah 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 dysfunction
Joery 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 Practice
Dianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
Page
of 1