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Radiology
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August 9, 2017
Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2
Julia P Owen, Polina Bukshpun, Nicholas Pojman, et al.
Neuron
|
February 28, 2012
Dual-mode modulation of Smad signaling by Smad-interacting protein Sip1 is required for myelination in the central nervous system
Qinjie Weng, Ying Chen, Haibo Wang, et al.
Science Translational Medicine
|
May 4, 2018
Arginine vasopressin in cerebrospinal fluid is a marker of sociality in nonhuman primates
Karen J Parker, Joseph P Garner, Ozge Oztan, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
February 14, 2015
Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication
Julian Jenkins, Vivian Chow, Lisa Blaskey, et al.
Plos One
|
August 8, 2012
The role of corpus callosum development in functional connectivity and cognitive processing
Leighton B N Hinkley, Elysa J Marco, Anne M Findlay, et al.
Neurology. Genetics
|
April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss
Ashley P L Marsh, Vesna Lukic, Kate Pope, et al.
Molecular Pharmacology
|
August 28, 2014
In silico identification of an aryl hydrocarbon receptor antagonist with biological activity in vitro and in vivo
Ashley J Parks, Michael P Pollastri, Mark E Hahn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 3, 2014
Aberrant white matter microstructure in children with 16p11.2 deletions
Julia P Owen, Yi Shin Chang, Nicholas J Pojman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 13, 2025
Refining Aicardi Syndrome diagnostic Criteria: an expert-based consensus using a modified Delphi approach
Silvia Masnada, Valentina De Giorgis, Umberto Carugo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?
Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 290) with videos related to
Sort By:
Page
of 29
Radiology
|
August 9, 2017
Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2
Julia P Owen, Polina Bukshpun, Nicholas Pojman, et al.
Neuron
|
February 28, 2012
Dual-mode modulation of Smad signaling by Smad-interacting protein Sip1 is required for myelination in the central nervous system
Qinjie Weng, Ying Chen, Haibo Wang, et al.
Science Translational Medicine
|
May 4, 2018
Arginine vasopressin in cerebrospinal fluid is a marker of sociality in nonhuman primates
Karen J Parker, Joseph P Garner, Ozge Oztan, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
February 14, 2015
Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication
Julian Jenkins, Vivian Chow, Lisa Blaskey, et al.
Plos One
|
August 8, 2012
The role of corpus callosum development in functional connectivity and cognitive processing
Leighton B N Hinkley, Elysa J Marco, Anne M Findlay, et al.
Neurology. Genetics
|
April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss
Ashley P L Marsh, Vesna Lukic, Kate Pope, et al.
Molecular Pharmacology
|
August 28, 2014
In silico identification of an aryl hydrocarbon receptor antagonist with biological activity in vitro and in vivo
Ashley J Parks, Michael P Pollastri, Mark E Hahn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 3, 2014
Aberrant white matter microstructure in children with 16p11.2 deletions
Julia P Owen, Yi Shin Chang, Nicholas J Pojman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 13, 2025
Refining Aicardi Syndrome diagnostic Criteria: an expert-based consensus using a modified Delphi approach
Silvia Masnada, Valentina De Giorgis, Umberto Carugo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?
Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.
Page
of 29