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

Dana Craiu

Showing results (21-30 of 62) with videos related to

Pageof 7
Sort By:
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2013
Subthalamic nucleus involvement in children: a neuroimaging pattern-recognition approachThangamadhan Bosemani, Cristina Anghelescu, Eugen Boltshauser, et al.
Maedica|May 3, 2014
Diagnostic approach of angelman syndromeDenis George Duca, Dana Craiu, Monica Boer, et al.
Human Molecular Genetics|January 2, 2015
Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assemblyKatia Hardies, Patrick May, Tania Djémié, et al.
Epilepsia|June 7, 2014
Co-occurring malformations of cortical development and SCN1A gene mutationsCarmen Barba, Elena Parrini, Roland Coras, et al.
Experimental and Therapeutic Medicine|January 3, 2022
Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from RomaniaMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.
Epilepsia|July 22, 2016
Testing patients during seizures: A European consensus procedure developed by a joint taskforce of the ILAE - Commission on European Affairs and the European Epilepsy Monitoring Unit AssociationSándor Beniczky, Miri Neufeld, Beate Diehl, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 4, 2016
Punctate white matter lesions in full-term infants with neonatal seizures associated with SLC13A5 mutationsLauren C Weeke, Eva Brilstra, Kees P Braun, et al.
Neurology|February 13, 2015
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizuresRhys H Thomas, Lin Mei Zhang, Gemma L Carvill, et al.
Epilepsy & Behavior Reports|April 15, 2025
Frequently asked questions and answers on Visually-Provoked (Photosensitive) epilepsyDorothée Kasteleijn-Nolst Trenité, Jayant Acharya, Fiona Mitchell Baumer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2025
Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective StudyMaria Nedelcu, Dana Craiu, Elena Neagu, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2013
Subthalamic nucleus involvement in children: a neuroimaging pattern-recognition approachThangamadhan Bosemani, Cristina Anghelescu, Eugen Boltshauser, et al.
Maedica|May 3, 2014
Diagnostic approach of angelman syndromeDenis George Duca, Dana Craiu, Monica Boer, et al.
Human Molecular Genetics|January 2, 2015
Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assemblyKatia Hardies, Patrick May, Tania Djémié, et al.
Epilepsia|June 7, 2014
Co-occurring malformations of cortical development and SCN1A gene mutationsCarmen Barba, Elena Parrini, Roland Coras, et al.
Experimental and Therapeutic Medicine|January 3, 2022
Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from RomaniaMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.
Epilepsia|July 22, 2016
Testing patients during seizures: A European consensus procedure developed by a joint taskforce of the ILAE - Commission on European Affairs and the European Epilepsy Monitoring Unit AssociationSándor Beniczky, Miri Neufeld, Beate Diehl, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 4, 2016
Punctate white matter lesions in full-term infants with neonatal seizures associated with SLC13A5 mutationsLauren C Weeke, Eva Brilstra, Kees P Braun, et al.
Neurology|February 13, 2015
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizuresRhys H Thomas, Lin Mei Zhang, Gemma L Carvill, et al.
Epilepsy & Behavior Reports|April 15, 2025
Frequently asked questions and answers on Visually-Provoked (Photosensitive) epilepsyDorothée Kasteleijn-Nolst Trenité, Jayant Acharya, Fiona Mitchell Baumer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2025
Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective StudyMaria Nedelcu, Dana Craiu, Elena Neagu, et al.
Pageof 7