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Pilvi Ilves

Showing results (21-30 of 41) with videos related to

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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.
Cancer Treatment and Research Communications|March 3, 2025
Population-based systematic enrolment of individuals ensures high lung cancer screening uptakeTanel Laisaar, Kadi Kallavus, Anneli Poola, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 26, 2018
Long-term neurodevelopmental outcome after perinatal arterial ischemic stroke and periventricular venous infarctionSilva Lõo, Pilvi Ilves, Mairi Männamaa, et al.
Pediatric Reports|April 27, 2026
Long-Term Outcomes After Childhood StrokeKerttu Kivisikk, Pilvi Ilves, Mairi Männamaa, et al.
Epilepsia Open|June 9, 2018
Epilepsy after perinatal stroke with different vascular subtypesRael Laugesaar, Ulvi Vaher, Silva Lõo, et al.
Neural Plasticity|January 12, 2017
Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal StrokeNigul Ilves, Pilvi Ilves, Rael Laugesaar, et al.
AJNR. American Journal of Neuroradiology|October 11, 2024
Pituitary Gland Duplication Syndrome: An International Imaging AnalysisUlrike Löbel, Martin Catala, Felice D'Arco, et al.
Brain and Behavior|November 16, 2016
Grey matter abnormalities in methcathinone abusers with a Parkinsonian syndromeJulius Juurmaa, Ricarda A L Menke, Pierre Vila, et al.
Journal of Child Neurology|December 20, 2013
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disordersUlvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.
Journal of Child Neurology|June 5, 2018
Incidence of Childhood Epilepsy in EstoniaKadi Veri, Inga Talvik, Ulvi Vaher, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
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.
Cancer Treatment and Research Communications|March 3, 2025
Population-based systematic enrolment of individuals ensures high lung cancer screening uptakeTanel Laisaar, Kadi Kallavus, Anneli Poola, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 26, 2018
Long-term neurodevelopmental outcome after perinatal arterial ischemic stroke and periventricular venous infarctionSilva Lõo, Pilvi Ilves, Mairi Männamaa, et al.
Pediatric Reports|April 27, 2026
Long-Term Outcomes After Childhood StrokeKerttu Kivisikk, Pilvi Ilves, Mairi Männamaa, et al.
Epilepsia Open|June 9, 2018
Epilepsy after perinatal stroke with different vascular subtypesRael Laugesaar, Ulvi Vaher, Silva Lõo, et al.
Neural Plasticity|January 12, 2017
Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal StrokeNigul Ilves, Pilvi Ilves, Rael Laugesaar, et al.
AJNR. American Journal of Neuroradiology|October 11, 2024
Pituitary Gland Duplication Syndrome: An International Imaging AnalysisUlrike Löbel, Martin Catala, Felice D'Arco, et al.
Brain and Behavior|November 16, 2016
Grey matter abnormalities in methcathinone abusers with a Parkinsonian syndromeJulius Juurmaa, Ricarda A L Menke, Pierre Vila, et al.
Journal of Child Neurology|December 20, 2013
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disordersUlvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.
Journal of Child Neurology|June 5, 2018
Incidence of Childhood Epilepsy in EstoniaKadi Veri, Inga Talvik, Ulvi Vaher, et al.
Pageof 5