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tiina talvik
tiina talvik
professor, department of paediatrics, University of Tartu
在 kliinikum.ee 的电子邮件经过验证
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Healthcare Access and Quality Index based on mortality from causes amenable to personal health care in 195 countries and territories, 1990–2015: a novel analysis from the …
RM Barber, N Fullman, RJD Sorensen, T Bollyky, M McKee, E Nolte, ...
The lancet 390 (10091), 231-266, 2017
5172017
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ...
Nature genetics 45 (9), 1067-1072, 2013
5122013
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
3182014
The phenotypic spectrum of SCN8A encephalopathy
J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ...
Neurology 84 (5), 480-489, 2015
2932015
De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
S Syrbe, U Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ...
Nature genetics 47 (4), 393-399, 2015
2852015
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
2692018
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
2552013
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
C Nava, C Dalle, A Rastetter, P Striano, CGF De Kovel, R Nabbout, ...
Nature genetics 46 (6), 640-645, 2014
2452014
Acutely and retrospectively diagnosed perinatal stroke: a population-based study
R Laugesaar, A Kolk, T Tomberg, T Metsvaht, M Lintrop, H Varendi, ...
Stroke 38 (8), 2234-2240, 2007
2072007
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
1972019
Resuscitation of newborn infants with 21% or 100% oxygen: follow-up at 18 to 24 months
OD Saugstad, S Ramji, SF Irani, S El-Meneza, EA Hernandez, M Vento, ...
Pediatrics 112 (2), 296-300, 2003
1852003
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
C Mignot, C Von Stülpnagel, C Nava, D Ville, D Sanlaville, G Lesca, ...
Journal of medical genetics 53 (8), 511-522, 2016
1722016
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
1622019
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
1472016
Shaken baby syndrome and a baby's cry
I Talvik, RC Alexander, T Talvik
Acta paediatrica 97 (6), 782-785, 2008
1432008
Prevalence of childhood epilepsy in Estonia
A Beilmann, A Napa, A Sööt, I Talvik, T Talvik
Epilepsia 40 (7), 1011-1019, 1999
1401999
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
1272016
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease
S Zagaglia, C Selch, JR Nisevic, D Mei, Z Michalak, ...
Neurology 91 (22), e2078-e2088, 2018
1162018
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
1152017
Cerebral blood‐flow velocities in predicting outcome of asphyxiated newborn infants
P Ilves, M Lintrop, T Metsvaht, U Vaher, T Talvik
Acta paediatrica 93 (4), 523-528, 2004
1122004
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