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Anna C Jansen

Showing results (81-90 of 97) with videos related to

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Journal of Medical Genetics|April 8, 2022
Overlapping cortical malformations in patients with pathogenic variants in <i>GRIN1</i> and <i>GRIN2B</i>Stefanie Brock, Annie Laquerriere, Florent Marguet, et al.
Frontiers in Neurology|April 9, 2021
TuberOus SClerosis registry to increAse disease awareness (TOSCA) Post-Authorisation Safety Study of Everolimus in Patients With Tuberous Sclerosis ComplexJ Chris Kingswood, Elena Belousova, Mirjana P Benedik, et al.
Frontiers in Neurology|September 28, 2020
Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA StudyAnna C Jansen, Stephanie Vanclooster, Petrus J de Vries, et al.
Journal of Neurodevelopmental Disorders|January 15, 2022
Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal periodAnatoly Korotkov, Mark J Luinenburg, Alessia Romagnolo, et al.
Pediatric Neurology|August 16, 2021
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management RecommendationsHope Northrup, Mary E Aronow, E Martina Bebin, et al.
Neuropathology and Applied Neurobiology|May 4, 2021
MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesisAnatoly Korotkov, Nam Suk Sim, Mark J Luinenburg, et al.
JMIR Research Protocols|May 5, 2026
Closing the Gap to Interventions for Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND): Protocol for a Longitudinal Study of TAND Severity, Predictors, and Caregiver Well-Being (TANDem-2)Petrus J de Vries, Nola Chambers, Erin Campbell, et al.
European Journal of Human Genetics : EJHG|July 1, 2026
CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disordersMatthias De Wachter, Mathijs B van der Lei, Amber Decleve, et al.
Pediatric Rheumatology Online Journal|October 17, 2022
Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases - a proof of concept studyMy Kieu Ha, Esther Bartholomeus, Luc Van Os, et al.
Brain : a Journal of Neurology|March 18, 2019
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamicsLaura V Vandervore, Rachel Schot, Esmee Kasteleijn, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|April 8, 2022
Overlapping cortical malformations in patients with pathogenic variants in <i>GRIN1</i> and <i>GRIN2B</i>Stefanie Brock, Annie Laquerriere, Florent Marguet, et al.
Frontiers in Neurology|April 9, 2021
TuberOus SClerosis registry to increAse disease awareness (TOSCA) Post-Authorisation Safety Study of Everolimus in Patients With Tuberous Sclerosis ComplexJ Chris Kingswood, Elena Belousova, Mirjana P Benedik, et al.
Frontiers in Neurology|September 28, 2020
Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA StudyAnna C Jansen, Stephanie Vanclooster, Petrus J de Vries, et al.
Journal of Neurodevelopmental Disorders|January 15, 2022
Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal periodAnatoly Korotkov, Mark J Luinenburg, Alessia Romagnolo, et al.
Pediatric Neurology|August 16, 2021
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management RecommendationsHope Northrup, Mary E Aronow, E Martina Bebin, et al.
Neuropathology and Applied Neurobiology|May 4, 2021
MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesisAnatoly Korotkov, Nam Suk Sim, Mark J Luinenburg, et al.
JMIR Research Protocols|May 5, 2026
Closing the Gap to Interventions for Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND): Protocol for a Longitudinal Study of TAND Severity, Predictors, and Caregiver Well-Being (TANDem-2)Petrus J de Vries, Nola Chambers, Erin Campbell, et al.
European Journal of Human Genetics : EJHG|July 1, 2026
CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disordersMatthias De Wachter, Mathijs B van der Lei, Amber Decleve, et al.
Pediatric Rheumatology Online Journal|October 17, 2022
Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases - a proof of concept studyMy Kieu Ha, Esther Bartholomeus, Luc Van Os, et al.
Brain : a Journal of Neurology|March 18, 2019
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamicsLaura V Vandervore, Rachel Schot, Esmee Kasteleijn, et al.
Pageof 10