Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Danique R M Vlaskamp

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Neurology|February 26, 2020
Author response: <i>SYNGAP1</i> encephalopathy: A distinctive generalized developmental and epileptic encephalopathyDanique R M Vlaskamp, Ingrid E Scheffer
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 9, 2014
Treatment of prolonged convulsive seizures in children; a single centre, retrospective, observational studyDanique R M Vlaskamp, Oebele F Brouwer, Petra M C Callenbach
Epilepsia|March 5, 2019
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering EpilepsyDanique R M Vlaskamp, Anne S Bassett, Joseph E Sullivan, et al.
Epilepsia Open|March 29, 2018
Copy number variation in a hospital-based cohort of children with epilepsyDanique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 29, 2016
Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsyDanique R M Vlaskamp, Patrick Rump, Petra M C Callenbach, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 10, 2021
Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsyDanique R M Vlaskamp, Patrick Rump, Petra M C Callenbach, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.
Epilepsia Open|July 28, 2023
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcomeNathan Buijsse, Floor E Jansen, Charlotte W Ockeloen, et al.
European Journal of Medical Genetics|August 21, 2018
PRRT2-related phenotypes in patients with a 16p11.2 deletionDanique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Neurology|February 26, 2020
Author response: <i>SYNGAP1</i> encephalopathy: A distinctive generalized developmental and epileptic encephalopathyDanique R M Vlaskamp, Ingrid E Scheffer
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 9, 2014
Treatment of prolonged convulsive seizures in children; a single centre, retrospective, observational studyDanique R M Vlaskamp, Oebele F Brouwer, Petra M C Callenbach
Epilepsia|March 5, 2019
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering EpilepsyDanique R M Vlaskamp, Anne S Bassett, Joseph E Sullivan, et al.
Epilepsia Open|March 29, 2018
Copy number variation in a hospital-based cohort of children with epilepsyDanique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 29, 2016
Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsyDanique R M Vlaskamp, Patrick Rump, Petra M C Callenbach, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 10, 2021
Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsyDanique R M Vlaskamp, Patrick Rump, Petra M C Callenbach, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.
Epilepsia Open|July 28, 2023
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcomeNathan Buijsse, Floor E Jansen, Charlotte W Ockeloen, et al.
European Journal of Medical Genetics|August 21, 2018
PRRT2-related phenotypes in patients with a 16p11.2 deletionDanique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
Pageof 2