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

Ulvi Vaher

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Frontiers in Neurology|October 16, 2023
The thalamus and basal ganglia are smaller in children with epilepsy after perinatal strokeUlvi Vaher, Norman Ilves, Nigul Ilves, et al.
Brain and Language|March 25, 2022
Language lateralization and outcome in perinatal stroke patients with different vascular typesNigul Ilves, Mairi Männamaa, Rael Laugesaar, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 10, 2024
Vascular syndrome predicts the development and course of epilepsy after perinatal strokeUlvi Vaher, Norman Ilves, Nigul Ilves, et al.
Frontiers in Stroke|January 16, 2026
General ability and specific cognitive functions are lower in children with epilepsy after perinatal ischemic strokeUlvi Vaher, Mairi Männamaa, Rael Laugesaar, et al.
European Journal of Medical Genetics|February 14, 2012
A novel c.2T > C mutation of the KDM5C/JARID1C gene in one large family with X-linked intellectual disabilityKatrin Ounap, Helen Puusepp-Benazzouz, Maire Peters, et al.
Neuropediatrics|September 7, 2016
CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the LiteratureStella Lilles, Inga Talvik, Klari Noormets, et al.
Child Neurology Open|May 16, 2017
Clinical Phenotype of De Novo <i>GNAO1</i> Mutation: Case Report and Review of LiteratureInga Talvik, Rikke S Møller, Merilin Vaher, et al.
Epilepsia Open|June 9, 2018
Epilepsy after perinatal stroke with different vascular subtypesRael Laugesaar, Ulvi Vaher, Silva Lõo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 18, 2014
Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalitiesEve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, et al.
Epilepsy Research|March 30, 2013
Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipinKadi Veri, Oivi Uibo, Tiina Talvik, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Frontiers in Neurology|October 16, 2023
The thalamus and basal ganglia are smaller in children with epilepsy after perinatal strokeUlvi Vaher, Norman Ilves, Nigul Ilves, et al.
Brain and Language|March 25, 2022
Language lateralization and outcome in perinatal stroke patients with different vascular typesNigul Ilves, Mairi Männamaa, Rael Laugesaar, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 10, 2024
Vascular syndrome predicts the development and course of epilepsy after perinatal strokeUlvi Vaher, Norman Ilves, Nigul Ilves, et al.
Frontiers in Stroke|January 16, 2026
General ability and specific cognitive functions are lower in children with epilepsy after perinatal ischemic strokeUlvi Vaher, Mairi Männamaa, Rael Laugesaar, et al.
European Journal of Medical Genetics|February 14, 2012
A novel c.2T > C mutation of the KDM5C/JARID1C gene in one large family with X-linked intellectual disabilityKatrin Ounap, Helen Puusepp-Benazzouz, Maire Peters, et al.
Neuropediatrics|September 7, 2016
CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the LiteratureStella Lilles, Inga Talvik, Klari Noormets, et al.
Child Neurology Open|May 16, 2017
Clinical Phenotype of De Novo <i>GNAO1</i> Mutation: Case Report and Review of LiteratureInga Talvik, Rikke S Møller, Merilin Vaher, et al.
Epilepsia Open|June 9, 2018
Epilepsy after perinatal stroke with different vascular subtypesRael Laugesaar, Ulvi Vaher, Silva Lõo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 18, 2014
Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalitiesEve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, et al.
Epilepsy Research|March 30, 2013
Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipinKadi Veri, Oivi Uibo, Tiina Talvik, et al.
Pageof 2