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Inga Talvik
Inga Talvik
Pediatric neurologist, Tallinn Children`s Hospital
Verified email at lastehaigla.ee
Title
Cited by
Cited by
Year
De novo variants in neurodevelopmental disorders with epilepsy
HO Heyne, T Singh, H Stamberger, R Abou Jamra, H Caglayan, D Craiu, ...
Nature genetics 50 (7), 1048-1053, 2018
2612018
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
A Suls, JA Jaehn, A Kecskés, Y Weber, S Weckhuysen, DC Craiu, ...
The American Journal of Human Genetics 93 (5), 967-975, 2013
2472013
The landscape of epilepsy-related GATOR1 variants
S Baldassari, F Picard, NE Verbeek, M van Kempen, EH Brilstra, G Lesca, ...
Genetics in Medicine 21 (2), 398-408, 2019
1892019
Epilepsy in tuberous sclerosis complex: findings from the TOSCA Study
R Nabbout, E Belousova, MP Benedik, T Carter, V Cottin, P Curatolo, ...
Epilepsia open 4 (1), 73-84, 2019
1562019
Phenotypic spectrum of GABRA1 From generalized epilepsies to severe epileptic encephalopathies
K Johannesen, C Marini, S Pfeffer, RS Møller, T Dorn, CE Niturad, ...
Neurology 87 (11), 1140-1151, 2016
1452016
Shaken baby syndrome and a baby's cry
I Talvik, RC Alexander, T Talvik
Acta paediatrica 97 (6), 782-785, 2008
1422008
Prevalence of childhood epilepsy in Estonia
A Beilmann, A Napa, A Sööt, I Talvik, T Talvik
Epilepsia 40 (7), 1011-1019, 1999
1421999
Gene panel testing in epileptic encephalopathies and familial epilepsies
RS Møller, LHG Larsen, KM Johannesen, I Talvik, T Talvik, U Vaher, ...
Molecular syndromology 7 (4), 210-219, 2016
1232016
Mutations in GABRB3 From febrile seizures to epileptic encephalopathies
RS Møller, TV Wuttke, I Helbig, C Marini, KM Johannesen, EH Brilstra, ...
Neurology 88 (5), 483-492, 2017
1132017
De NovoSCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and …
U Vaher, M Nõukas, T Nikopensius, M Kals, T Annilo, M Nelis, K Õunap, ...
Journal of child neurology 29 (12), NP202-NP206, 2014
822014
Inflicted traumatic brain injury (ITBI) or shaken baby syndrome (SBS) in Estonia
I Talvik, T Metsvaht, K Leito, H Põder, P Kool, M Väli, M Lintrop, A Kolk, ...
Acta paediatrica 95 (7), 799-804, 2006
782006
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy
K Reinson, E Õiglane‐Shlik, I Talvik, U Vaher, A Õunapuu, M Ennok, ...
American journal of medical genetics Part A 170 (8), 2173-2176, 2016
732016
Changes in Cerebral and Visceral Blood Flow Velocities in Asphyxiated Term Neonates With Hypoxic‐Ischemic Encephalopathy
P Ilves, M Lintrop, I Talvik, K Muug, L Maipuu
Journal of Ultrasound in Medicine 28 (11), 1471-1480, 2009
602009
The screening of SLC6A8 deficiency among Estonian families with X‐linked mental retardation
H Puusepp, K Kall, GS Salomons, I Talvik, M Männamaa, R Rein, ...
Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2010
582010
Incidence of childhood epilepsy in Estonia
A Beilmann, A Napa, M Hämarik, A Sööt, I Talvik, T Talvik
Brain and Development 21 (3), 166-174, 1999
581999
Epidemiology of childhood stroke in Estonia
R Laugesaar, A Kolk, Ü Uustalu, P Ilves, T Tomberg, I Talvik, K Köbas, ...
Pediatric neurology 42 (2), 93-100, 2010
502010
Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia
S Puusepp, K Reinson, S Pajusalu, Ü Murumets, E Õiglane-Shlik, R Rein, ...
Molecular genetics and metabolism reports 15, 80-89, 2018
472018
Therapie idiopathischer Kopfschmerzen im Kindes-und Jugendalter
S Evers, P Kropp, R Pothmann, F Heinen, F Ebinger
Nervenheilkunde 27 (12), 1127-1137, 2008
472008
Presumed perinatal stroke: risk factors, clinical and radiological findings
P Ilves, R Laugesaar, D Loorits, A Kolk, T Tomberg, S Lõo, I Talvik, ...
Journal of child neurology 31 (5), 621-628, 2016
442016
Developmental changes in cerebral and visceral blood flow velocity in healthy neonates and infants
P Ilves, M Lintrop, I Talvik, K Muug, K Asser, M Veinla
Journal of Ultrasound in Medicine 27 (2), 199-207, 2008
392008
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