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Neurology
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February 26, 2020
Author response: <i>SYNGAP1</i> encephalopathy: A distinctive generalized developmental and epileptic encephalopathy
Danique 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 study
Danique R M Vlaskamp, Oebele F Brouwer, Petra M C Callenbach
Epilepsia
|
March 5, 2019
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy
Danique 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 epilepsy
Danique 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 epilepsy
Danique 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 epilepsy
Danique 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 detection
Mark 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 variants
Géza 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 outcome
Nathan 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 deletion
Danique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Neurology
|
February 26, 2020
Author response: <i>SYNGAP1</i> encephalopathy: A distinctive generalized developmental and epileptic encephalopathy
Danique 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 study
Danique R M Vlaskamp, Oebele F Brouwer, Petra M C Callenbach
Epilepsia
|
March 5, 2019
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy
Danique 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 epilepsy
Danique 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 epilepsy
Danique 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 epilepsy
Danique 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 detection
Mark 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 variants
Géza 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 outcome
Nathan 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 deletion
Danique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
Page
of 2