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Child Neurology Open
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May 16, 2017
Clinical Phenotype of De Novo <i>GNAO1</i> Mutation: Case Report and Review of Literature
Inga 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 uptake
Tanel 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 infarction
Silva Lõo, Pilvi Ilves, Mairi Männamaa, et al.
Pediatric Reports
|
April 27, 2026
Long-Term Outcomes After Childhood Stroke
Kerttu Kivisikk, Pilvi Ilves, Mairi Männamaa, et al.
Epilepsia Open
|
June 9, 2018
Epilepsy after perinatal stroke with different vascular subtypes
Rael Laugesaar, Ulvi Vaher, Silva Lõo, et al.
Neural Plasticity
|
January 12, 2017
Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal Stroke
Nigul Ilves, Pilvi Ilves, Rael Laugesaar, et al.
AJNR. American Journal of Neuroradiology
|
October 11, 2024
Pituitary Gland Duplication Syndrome: An International Imaging Analysis
Ulrike Löbel, Martin Catala, Felice D'Arco, et al.
Brain and Behavior
|
November 16, 2016
Grey matter abnormalities in methcathinone abusers with a Parkinsonian syndrome
Julius 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 disorders
Ulvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.
Journal of Child Neurology
|
June 5, 2018
Incidence of Childhood Epilepsy in Estonia
Kadi Veri, Inga Talvik, Ulvi Vaher, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 41) with videos related to
Sort By:
Page
of 5
Child Neurology Open
|
May 16, 2017
Clinical Phenotype of De Novo <i>GNAO1</i> Mutation: Case Report and Review of Literature
Inga 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 uptake
Tanel 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 infarction
Silva Lõo, Pilvi Ilves, Mairi Männamaa, et al.
Pediatric Reports
|
April 27, 2026
Long-Term Outcomes After Childhood Stroke
Kerttu Kivisikk, Pilvi Ilves, Mairi Männamaa, et al.
Epilepsia Open
|
June 9, 2018
Epilepsy after perinatal stroke with different vascular subtypes
Rael Laugesaar, Ulvi Vaher, Silva Lõo, et al.
Neural Plasticity
|
January 12, 2017
Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal Stroke
Nigul Ilves, Pilvi Ilves, Rael Laugesaar, et al.
AJNR. American Journal of Neuroradiology
|
October 11, 2024
Pituitary Gland Duplication Syndrome: An International Imaging Analysis
Ulrike Löbel, Martin Catala, Felice D'Arco, et al.
Brain and Behavior
|
November 16, 2016
Grey matter abnormalities in methcathinone abusers with a Parkinsonian syndrome
Julius 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 disorders
Ulvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.
Journal of Child Neurology
|
June 5, 2018
Incidence of Childhood Epilepsy in Estonia
Kadi Veri, Inga Talvik, Ulvi Vaher, et al.
Page
of 5