See veebileht kasutab küpsiseid kasutaja sessiooni andmete hoidmiseks. Veebilehe kasutamisega nõustute ETISe kasutustingimustega. Loe rohkem
Olen nõus

Inga Talvik

https://www.etis.ee/CV/Inga_Talvik/est
6.05.1965
inga.talvik@ut.ee

Teenistuskäik

Töökohad ja ametid
01.02.2019–31.12.2022   
Tartu Ülikool, Meditsiiniteaduste valdkond, kliinilise meditsiini instituut, lasteneuroloogia teadur (0,30)
2017–...   
SA Tallinna Lastehaigla, Neuroloogia ja rehabilitatsiooni osakond, juhataja (1,00)
01.01.2016–01.09.2017   
SA Tallinna Lastehaigla, Neuroloog (1,00)
01.09.2014–31.12.2015   
Tartu Ülikool, Arstiteaduskond, Lastekliinik, lasteneuroloogia dotsent (0,50)
01.09.2009–31.08.2014   
Tartu Ülikool, Arstiteaduskond, Lastekliinik, lasteneuroloogia dotsent (0,50)
01.09.2008–31.08.2009   
Tartu Ülikool, Arstiteaduskond, Lastekliinik, lasteneuroloogia vanemassistent (0,50)
15.02.2008–31.05.2008   
Tartu Ülikool, Arstiteaduskond, Lastekliinik, spetsialist (0,30)
2008–2009   
Tartu Ülikool, Arstiteaduskond, Lastekliinik, Pediaatria õppetool, lasteneuroloogia vanemassistent (0,50)
2005–31.12.2015   
SA Tartu Ülikooli Kliinikum, Tartu Ülikooli Kliinikumi Lastekliinik, vanemarst-õppejõud (1,00)
01.01.2005–31.12.2010   
SA TÜK Lastekliinik
 
 
Haridustee
1983–1989   
Tartu Ülikool Arstiteaduskond
1972–1983   
Miina Härma nimeline Tartu II Keskkool
 
 
Teadusorganisatsiooniline ja -administratiivne tegevus
2013−...   
Eesti Lasteneuroloogide Selts - president
2009−...   
Eesti epilepsia vastane liiga - juhatuse liige
2006−...   
Euroopa Lasteneuroloogide Assotsiatsioon
2000−...   
Eesti inimgeneetika ühing
2006−2015   
Eesti Epilepsia Liit - juhatuse esimees
 
 
Loometöö
Huvitatud teadvustööst epilepsiast
 
 
Lisainfo
Neuroloog- lasteneuroloog

Kvalifikatsioon

Teaduskraadid
Inga Talvik, doktorikraad, 2007, (juh) Tiina Talvik, Inflicted traumatic brain injury/shaken baby syndrome in Estonia- epidemiology and outcome (Raputatud lapse sündroom Eestis- epidemioloogia ja kaugtulemused), Tartu Ülikool, Arstiteaduskond.
 
 

Jooksvad projektid

Lõppenud projektid

Juhendamisel väitekirjad

Publikatsioonid

Klass
Aasta
Publikatsioon
 
1.1.
2017
Møller, Rikke S; Wuttke, Thomas V; Helbig, Ingo; Marini, Carla; Johannesen, Katrine M; Brilstra, Eva H; Vaher, Ulvi; Borggraefe, Ingo; Talvik, Inga; Talvik, Tiina; Kluger, Gerhard; Francois, Laurence L; Lesca, Gaetan; de Bellescize, Julitta; Blichfeldt, Susanne; Chatron, Nicolas; Holert, Nils; Jacobs, Julia; Swinkels, Marielle; Betzler, Cornelia ... Maljevic, Snezana (2017). Mutations in GABRB3: From febrile seizures to epileptic encephalopathies. Neurology, 88 (5), 483−492.10.1212/WNL.0000000000003565.
1.1.
2017
Ilves,Nigul; Ilves, PIlvi; Laugesaar, Rael; Juurmaa, Julius; Männamaa, Mairi; Lõo, Silva; Loorits, Dagmar; Tomberg, Tiiu; Kolk, Anneli; Talvik, Inga; Talvik, Tiina (2017). Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal Stroke. Neural Plasticity, 2016, 11−11. DOI: 10.1155/2016/2306406.
5.2.
2017
Ilves, Nigul; Ilves, Pilvi; Laugesaar, Rael; Juurmaa, Julius; Männamaa, Mairi; Lõo, Silva; Loorits, Dagmar; Tomberg, Tiiu; Kolk, Anneli; Talvik, Inga; Talvik, Tiina; (2017). Correlations in resting-state functional networks and cognitive functions in children with perinatal stroke and healthy controls. In: . European Congress of Magnetic Resonance in Neuropediatrics, Tübingen Germany, June 8 to 10, 2017.
1.1.
2016
Reinson, Karit; Õiglane-Shlik, Eve; Talvik, Inga; Vaher, Ulvi; Õunapuu, Anne; Ennok, Margus; Teek, Rita; Pajusalu, Sander; Murumets, Ülle; Tomberg, Tiiu; Puusepp, Sanna; Piirsoo, Andres; Reimand, Tiia; Õunap, Katrin (2016). Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. American Journal of Medical Genetics Part A, 170 (8), 2173−2176. DOI: 10.1002/ajmg.a.37678.
1.1.
2016
Lilles, Stella; Talvik, Inga; Noormets, Klari; Vaher, Ulvi; Õunap, Katrin; Reimand, Tiia; Sander, Valentin; Ilves, Pilvi; Talvik, Tiina (2016). CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature. Neuropediatrics, 47 (6), 361−367. DOI: 10.1055/s-0036-1586730.
1.1.
2016
Pajusalu, S.; Talvik, I.; Noormets, K.; Talvik, T.; Põder, H.; Joost, K.; Puusepp, S.; Piirsoo, A.; Stenzel, W.; Goebel, HH.; Nikopensius, T.; Annilo, T.; Nõukas, M.; Metspalu, A.; Õunap, K.; Reimand, T. (2016). De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion. Neuromuscular Disorders, 26 (3), 236−239. DOI: 10.1016/j.nmd.2015.11.011.
1.1.
2016
Johannesen, Katrine; Marini, Carla; Pfeffer, Siona; Møller, Rikke S; Dorn, Thomas; Niturad, Cristina Elena; Gardella, Elena; Weber, Yvonne; Søndergård, Marianne; Hjalgrim, Helle; Nikanorova, Mariana; Becker, Felicitas; Larsen, Line H G; Dahl, Hans A; Maier, Oliver; Mei, Davide; Biskup, Saskia; Klein, Karl M; Reif, Philipp S; Rosenow, Felix ... Maljevic, Snezana (2016). Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. Neurology, 87 (11), 1140−1151.10.1212/WNL.0000000000003087.
1.2.
2016
Møller, Rikke S; Larsen, Line H G; Johannesen, Katrine M; Talvik, Inga; Talvik, Tiina; Vaher, Ulvi; Miranda, Maria J; Farooq, Muhammad; Nielsen, Jens E K; Svendsen, Lene Lavard; Kjelgaard, Ditte B; Linnet, Karen M; Hao, Qin; Uldall, Peter; Frangu, Mimoza; Tommerup, Niels; Baig, Shahid M; Abdullah, Uzma; Born, Alfred P; Gellert, Pia ... Dahl, Hans A (2016). Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. Molecular Syndromology, 7 (4), 210−219.
5.2.
2016
J. Katus, I. Talvik, S. Margus, R. Laugesaar, D. Loorits, V. Tolpats, E. Õiglane-Šlik, T. Talvik, P. Ilves. (2016). 7-aastase poisi basilaartromboosi ravi intaarteriaalse trombektoomia abil - haigusjuhu kirjeldus. Eesti Lastearstide Seltsi XXI kongressi abstraktide kogumik (47).Eesti Lastearstide Seltsi XXI kongress, 2.-4. juuni 2016, Tallinn..
5.2.
2016
Jesse K, Laugesaar R, Lõo S, Ilves P, Kolk A, Talvik I, Talvik T. (2016). Gross motor function in children after perinatal ishemic stroke. In: International Conference on Cerebral Palsy and other Childhood-onset Disabilities 2016 Abstract Book. International Conference on Cerebral Palsy and other Childhood-onset Disabilities, Stockholm, 1–4 June 2016.
5.2.
2016
Katus Jaan, Talvik Inga, Laugesaar Rael, Õiglane-Šlik Eve, Margus Sulev, Loorits Dagmar, Talvik Tiina, Ilves Pilvi. (2016). Intraarterial thrombectomy in a previously healthy 7-years-old boy with basilar artery thrombosis. In: Baltic Congress of Radiology 2016 Abstract book (32−33).Baltic Congress of Radiology, October 6-8, 2016, Liepaja, Latvia.
5.2.
2016
R. Laugesaar, S. Lõo, U. Vaher, M. Männamaa, A. Kolk, I. Talvik, E. Õiglane-Šlik, V. Sander, D. Loorits, T. Tomberg, T. Talvik, P. Ilves. (2016). Epilepsia perinataalset insulti põdenud lastel. Eesti Lastearstide Seltsi XXI kongressi abstraktide raamat (30). Eesti Lastearstide Seltsi XXI kongress. 2.-4. juuni 2016, Tallinn..
5.2.
2016
N. Ilves, P. Ilves, R. Laugesaar, J. Juurmaa, S. Lõo, M. Männamaa, D. Loorits, T. Tomberg, A. Kolk, I. Talvik, T. Talvik. (2016). Erinevused rahuoleku funktsionaalses konnektiivsuses perinataalse arteriaalse isheemilise insuldi ja hilise diagnoosiga periventrikulaarse venoosse insuldiga lastel. Eesti Lastearstide Seltsi XXI Kongressi abstraktide kogumik (32). Eesti Lastearstide Seltsi XXI Kongress. 2.-4. juuni 2016, Tallinn..
1.1.
2014
Žilina, O.; Kahre, T.; Talvik, I.; Õiglane-Shlik, E.; Tillmann, V.; Õunap, K. (2014). Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome. European Journal of Medical Genetics, 57 (6), 279−283. DOI: 10.1016/j.ejmg.2014.03.007.
1.1.
2014
Õiglane-Shlik, E.; Puusepp, S.; Talvik, I.; Vaher, U.; Rein, R.; Tammur, P.; Reimand, T.; Teek, R.; Žilina, O.; Tomberg, T.; Õunap, K. (2014). Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities. European Journal of Paediatric Neurology, 18 (3), 338−346. DOI: 10.1016/j.ejpn.2014.01.008.
1.1.
2014
Vaher, Ulvi; Nõukas, Margit; Nikopensius, Tiit; Kals, Mart; Annilo, Tarmo; Nelis, Mari; Õunap, Katrin; Reimand, Tiia; Talvik, Inga; Ilves, Pilvi; Piirsoo, Andres; Seppet, Enn; Metspalu, Andres; Talvik, Tiina (2014). De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders. Journal of Child Neurology, 29 (12), 202−206. DOI: 10.1177/0883073813511300.
1.1.
2013
Suls, A.; Jaehn, JA.; Kecskés, A.; Weber, Y.; Weckhuysen, S.; Craiu, DC.; Siekierska, A.; Djémié, T.; Afrikanova, T.; Gormley, P.; von Spiczak, S.; Kluger, G.; Iliescu, CM.; Talvik, T.; Talvik, I.; Meral, C.; Caglayan, HS.; Giraldez, BG.; Serratosa, J.; Lemke, JR. ... Helbig, I. EuroEPINOMICS RES Consortium (2013). De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. The American Journal of Human Genetics, 93 (5), 967−975.10.1016/j.ajhg.2013.09.017.
1.1.
2013
Veri, K; Uibo, O; Talvik, T; Talvik, I; Metsküla, K; Napa, A; Vaher, U; Õiglane-Šlik, E; Rein, R; Kolk, A; Traat, A; Uibo, R. (2013). Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipin. Epilepsy Research, 105, 86−91.10.1016/j.eplepsyres.2013.02.009.
5.1.
2013
Tammur, P.; Reimand, T.; Žilina, O.; Talvik, I.; Ilisson, P.; Ilus, T.; Toit, P.; Kuuse, K.; Õunap, K. (2013). Copy-number variations at 16p11.2 in Estonian patients. European Journal of Human Genetics, 21: European Human Genetics Conference 2013; June 8 - 11, 2013; Palais des Congrès, Paris, France. Nature Publishing Group, 157−157.
5.2.
2013
Pajusalu, S.; Õiglane-Šlik, E.; Talvik, I.; Teek, R.; Žilina, O.; Kuuse, K.; Reimand, T.; Õunap, K. (2013). Clinical characterization of six patients with 15q13.2-q13.3 microdeletion. In: . First International GENCODYS Conference, Integrative Networks in Intellectual Disabilities; Paphos, Cyprus; 14-17 April 2013.
5.2.
2013
Noormets, Klari; Õunap, Katrin; Talvik, Tiina; Talvik, Inga (2013). CDKL5 gene related epileptic encephalopathy in Estonia: a case presentation. Seminars in Neurology: 12th Congress of the Baltic Child Neurology Association, Kaunas, Lithuania, 30 May - 01 June 2013. S45−S45.
1.1.
2012
Joost, K.; Rodenburg, R.J.; Piirsoo, A.; van den Heuvel, L.; Žordania, R.; Põder, H.; Talvik, I.; Kilk, K.; Soomets, U.; Õunap, K. (2012). A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children. Molecular Syndromology, 3 (3), 113−119.10.1159/000341375.
1.1.
2012
Tiigimäe-Saar, J.; Leibur, E.; Kolk, A.; Talvik, I.; Tamme, T. (2012). Use of Botulinum neurotoxin A in uncontrolled salivation in children with cerebral palsy. A pilot study. International Journal of Oral and Maxillofacial Surgery, 41 (12), 1540−1545.10.1016/j.ijom.2012.09.015.
1.1.
2012
Krabbi, K.; Joost, K.; Zordania, R.; Talvik, I.; Rein, R.; Huijmans, J. G. M.; Verheijen, F. V.; Õunap, K (2012). The live-birth prevalence of mucopolysaccharidoses in Estonia. Genetic Testing and Molecular Biomarkers, 16 (8), 846−849.10.1089/gtmb.2011.0307.
1.1.
2012
Talvik, I.; Vibo, R.; Liik, M.; Haldre, S.; Talvik, T. (2012). Epileptic laughter: 2 case reports. Medicina (Kaunas), 48 (7), 359−363.
1.3.
2012
Laugesaar, Rael; Pajusalu, Sander; Toome, Liis; Kolk, Anneli; Tomberg, Tiiu; Ilves, Pilvi; Eelmäe, Imbi; Talvik, Inga; Talvik, Tiina (2012). Sinovenoosne tromboos lastel: kirjanduse ülevaade ja kogemus Eestis. Eesti Arst, 91 (11), 604−609.
3.1.
2012
Talvik, Tiina; Kirkham, Fenella; Metsvaht, Tuuli; Talvik, Inga (2012). Principles and Practice of Child Neurology in Infancy. In: Colin Kennedy (Ed.). Principles and Practice of Child Neurology in Infancy (179−204).. Principles and Practice of Child Neurology in Infancy , Mac Keith Press, London UK 6 Market Road, London N7 9PW, UK : Wiley InterScience.
5.1.
2012
Kall, K.; Reimand, T.; Talvik, I.; Pop, A.; Salomons, GS.; Õunap, K. (2012). Biochemical diagnostics of creatine transporter deficiency in Estonia. JOURNAL OF INHERITED METABOLIC DISEASE, 35 (suppl 1): Annual Symposium of the Society for the Study of Inborn Errors of Metabolism; Birmingham, UK, 4 – 7 September 2012. Springer, S54−S54.
5.2.
2012
Mikkel, S.; Boriskina, K.; Talvik, I.; Reimand, T.; Everaus, H. (2012). Familiar hemophagocytic lymphohistiocytosis - case report. Abstract book 8th Baltic Conference on Hematology: 8th Baltic Conference on Hematology; 12-14.04.2012; Tallinn. , 77−78.
5.2.
2012
Uibo, O.; Veri, K.; Talvik, I.; Metsküla, K.; Traat, A.; Heilman, K.; Talvik, T.; Uibo, R. (2012). Autoantibodies to glutamic acid decarboxylase in children with newly-diagnosed epilepsy: rare association with type i diabetes. Abstracts.: 12th International Conference on the Immunology of Diabetes; Victoria, Kanada; 15-19.06.2012. , 151−152.
5.2.
2012
Laugesaar, R.; Pajusalu, S.; Toome, L.; Kolk, A.; Tomberg, T.; Ilves, P.; Eelmäe, I.; Talvik, I.; Talvik, T. (2012). Paediatric cerebral sinovenous thrombosis in Estonia. Abstract book: The 7th Baltic Congress of Neurology, Tartu, Estonia, May 9-12, 2012. 162.
1.1.
2011
Joost, K.; Tammur, P.; Teek, R.; Žilina, O.; Peters, M.; Kreile, M.; Lace, B.; Žordania, R.; Talvik, I.; Õunap, K. (2011). Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency. Molecular Syndromology, 1 (6), 311−315. DOI: 10.1159/000331323.
3.3.
2011
Metsvaht, Tuuli; Vainumäe, Inga; Gontmacher, Aasa; Grünberg, Heli; Eelmäe, Imbi; Maipuu, Lea; Tamm, Eda; Torm, Siiri; Pütsepp, Aime; Sizarov, Aleksandr; Laan, Mari; Virro, Silvia; Varendi, Heili; Veinla, Maie; Mägi, Marja-Liis; Külasepp, Piret; Kallas, Eha; Talvik, Inga; Kolk, Anneli; Talvik, Tiina ... Kõrgvee, Lenne-Triin (2011). Valvearsti teatmik. Heli Grünberg (Toim.). Valvearsti teatmik. . Tartu: Tartu University Press.
5.2.
2011
Reimand, T.; Uibo, O.; Luts, K.; Talvik, I.; Zhilina, O.; Muru, K.; Õunap, K. (2011). Microdeletion 10q23 and juvenile polyposis syndrome: a case report. European Human GenetiConference cs 2011, Amsterdam RAI, The Netherlands, May 28 - 31, 2011. x, x.
5.2.
2011
Tammur, P.; Reimand, T.; Õiglane-Šlik, E.; Teek, R.; Zilina, O.; Talvik, I.; Ilisson, P.; Ilus, T.; Kuuse, K.; Jürgenson, M.; Õunap, K. (2011). Four cases of 1p36 microdeletion and their clinical characterization. 8th European Cytogenetics Conference, Porto, Portugal, July 2-5, 2011.
1.1.
2010
Talvik, I.; Segawa, M.; Veri, K.; Gross-Paju, K.; Talvik, T. (2010). Cases of dopa-responsive dystonia (Segawa disease) in Estonia. Brain Dev, 32 (5), 428−431.10.1016/j.braindev.2009.04.007.
1.1.
2010
Talvik, Inga; Peet, Aleksandr; Laugesaar, Rael; Lintrop, Mare; Talvik, Tiina (2010). Vehicle-associated closed trauma-induced stroke in a 27-day-old girl. Medicina (Kaunas), 624−627.
1.1.
2010
Ilves, Pilvi; Lintrop, Mare; Talvik, Inga; Sisko, Annika; Talvik, Tiina (2010). Predictive value of clinical and radiological findings in inflicted traumatic brain injury. Acta Paediatrica, 99 (9), 1329−1336.10.1111/j.1651-2227.2010.01820.x.
1.1.
2010
Laugesaar, R.; Kolk, A.; Uustalu, Ü.; Ilves, P.; Tomberg, T.; Talvik, I.; Köbas, K.; Sander, V.; Talvik, T. (2010). Epidemiology of childhood stroke in Estonia. Pediatric Neurology, 42 (2), 93−100.
1.3.
2010
Lintrop, Mare; Talvik, Inga; Tolpats, Viive; Nellis, Georgi; Mikkel, Sirje; Padari, Helgi; Napa, Aita; Ilves, Pilvi (2010). Posterioorse reversiibelse entsefalopaatia sündroom (PRES): kirjanduse ülevaade ja kahe haigusjuhu kirjeldus. Eesti Arst, 89 (3), 191−199.
1.3.
2010
Inga Talvik, Reili Rebane, Tiia Reimand, Aita Napa, Tiina Talvik (2010). Ravile raskesti alluv epilepsia 20. rõngaskromosoomi sündroomi korral: kirjanduse ülevaade ja haigusjuhu kirjeldus. Eesti Arst, 89 (10), 646−650.
5.2.
2010
Reimand, T.; Uibo, O.; Luts, K.; Talvik, I.; Zilina, O.; Muru, K.; Õunap, K. (2010). Mikrodeletsioon 10q23.1-q23.3 juveniilse polüpoosi põhjusena. (45−45). Eesti Lastearstide 19.kongress.
5.2.
2010
Veri, K.; Uibo, O.; Metsküla, K.; Talvik, I.; Napa, A.; Vaher, U.; Rein, R.; Õiglane-Slik, E.; Kolk, A.; Talvik, T.; Uibo, R. (2010). Autoantikehade esinemine epilepsia diagnoosiga lastel. (20−20). Eesti Lastearstide 19.kongress.
5.2.
2010
Ilves, Pilvi; Lintrop, Mare; Talvik, Inga; Sisko, Annika (2010). Correlations between late radiological findings and long-term neurodevelopmental outcome in inflicted traumatic brain injury. Pediatric Radiology, 40: ESPR 2010; Bordeaux, France; 7-10 June 2010. Springer, 1076.
5.2.
2010
Lintrop, Mare; Ilves, Pilvi; Tolpats, Viive; Talvik, Inga (2010). Posterior reversible encephalopathy syndrome: two cases in children. Pediatric Radiology: ESPR 2010; Bordeaux, France; 7-10 June. Springer, 1116.
5.2.
2010
Vainumäe, I.; Rägo, T.; Metsvaht, T.; Mikkel, S.; Talvik, I.; Vals, M.-A.; Luts, K.; Kahre, T. (2010). Wilsoni tõbi lastel. 1996–2009 TÜ Kliinikumi lastekliinikus diagnoositud juhud. Eesti Arst, 89: Eesti lastearstide 19. kongress 3.-5.-06.2010. Tallinn, 62−62. (lisa 1).
1.1.
2009
Ilves, P.; Lintrop, M.; Talvik, I.; Muug, K.I; Maipuu, L. (2009). Changes in cerebral and visceral blood flow velocities in asphyxiated term infants with hypoxic ischemic encephalopathy. Journal of Ultrasound in Medicine, 28 (11), 1471−1480.
1.1.
2009
Talvik, I.; Peet, A.; Talvik, T. (2009). Three-year follow-up of a girl with chronic paroxysmal hemicrania. Pediatric Neurology, 1, 68−69.
1.1.
2009
Ilves, P.; Lintrop, M.; Talvik, I.; Muug, K.; Maipuu, L.; Metsvaht, T. (2009). Low cerebral blood flow velocity and head circumference in infants with severe hypoxic ischemic encephalopathy and poor outcome. Acta Paediatrica, 98 (3), 459−465. DOI: 10.1111/j.1651-2227.2008.01119.x.
6.7.
2009
Talvik, Inga; Väli, Marika; Mirka, Gerli; Ilves, Pilvi; Lintrop, Mare; Sisko, Annika; Kolk, Anneli; Talvik, Tiina; Alexander, Randell (2009). X International Conference of Baltic Child Neurology Association (BCNA), Tartu, Estonia, may 6-9, 2009 [Videosalvestis] : Session III: Traumatic brain injury. International Conference of Baltic Child Neurology Association(10 :2009 :Tartu). Tartu: TÜ IT Õppetehnika talitus. (TÜ filmiarhiiv).
1.1.
2008
Ilves, Pilvi; Lintrop, Mare; Talvik, Inga; Muug, Külli; Asser, Karin; Veinla, Maie (2008). Developmental changes in cerebral and visceral blood flow velocity in healthy neonates and infants. Journal of Ultrasound in Medicine, 27 (2), 199−207.
1.1.
2008
Talvik, I.; Alexander, R.; Talvik, T. (2008). Shaken baby syndrome and a baby's cry. Acta Paediatrica, 97 (6), 782-−785.
1.1.
2008
Ventsel, G.; Kolk, A.; Talvik, I.; Väli, M.; Vaikmaa, M.; Talvik, T. (2008). The Incidence of Childhood Traumatic Brain Injury in Tartu and Tartu County in Estonia. Neuroepidemiology, 30 (1), 20−24. DOI: 10.1159/000113302.
1.1.
2007
Vaidla, E.; Talvik, I.; Kulla, A.; Sibul, H.; Maasalu, K.; Metsvaht, T.; Piirsoo, A.; Talvik, T. (2007). Neonatal spinal muscular atrophy type 1 with bone fractures and heart defect. Journal of Child Neurology, 22 (1), 67−70. DOI: 10.1177/0883073807299954.
1.1.
2007
Talvik, I.; Männamaa, M.; Jüri, P.; Leito, K.; Põder, H.; Hämarik, M.; Kool, P.; Talvik, T. (2007). Outcome of infants with inflicted traumatic brain injury (Shaken baby Syndrome) in Estonia. Acta Paediatrica, 96 (8), 1164−1168. DOI: 10.1111/j.1651-2227.2007.00362.x.
1.3.
2007
Talvik, I.; Lintrop, M.; Metsvaht, T.; Talvik, T. (2007). Millal mõelda raputatud lapse sündroomile: kirjanduse ülevaade ning haigusjuhu kirjeldus. Eesti Arst, 86 (6), 420−423.
1.3.
2007
Talvik, I.; Koch, K.; Talvik, T. (2007). Krooniline paroksüsmaalne hemikraania: kirjanduse ülevaade ja 3 aasta 10 kuu vanuse tütarlapse edukas ravitulemus indometatsiiiniga. Eesti Arst, 86 (8), 517−520.
2.3.
2007
Talvik, I. (2007). Inflicted traumatic brain injury / shaken baby syndrome in Estonia - epidemiology and outcome. (Tartu Ülikool). Tartu University Press.
1.1.
2006
Talvik, I.; Koch, K.; Kolk, A.; Talvik, T. (2006). Chronic paroxysmal hemicrania in 3-year 10 month-old female. Pediatric Neurology, 34 (3), 225−227.
1.1.
2006
Vaidla , E.; Talvik, I.; Kulla, A.; Kahre, T.; Hämarik, M.; Napa , A.; Metsvaht, T.; Piirsoo, A.; Talvik , T. (2006). Descriptive epidemiology of spinal muscular atrophy type I in Estonia. Neuroepidemiology, 27 (3), 164−168.
1.1.
2006
Talvik, I.; Metsvaht, T.; Leito, K.; Põder, H.; Kool, P.; Väli, M.; Lintrop, M.; Kolk, A.; Talvik, T. (2006). Inflicted traumatic brain injury (ITBI) or shaken baby syndrome (SBS) in Estonia. Acta Paediatrica, 95 (7), 799−804. DOI: 10.1080/08035250500464923.
1.3.
2006
Talvik, I.; Veri, K.; Gross-Paju, K.; Kolk, A.; Talvik, T. (2006). Dopamiintundlik düstoonia: kirjanduse ülevaade ja haigusjuhu kirjeldus. Eesti Arst, 85 (12), 841−844.
5.2.
2004
Lintrop, Mare; Ilves, Pilvi; Talvik, Inga (2004). Aju ultraheliuuringud raputatud lapse diagnostikas. Eesti Arst, 83 (5), 336.
1.1.
2003
Talkop, U.A.; Kahre, T.; Napa, A.; Talvik, I.; Soot, A.; Piirsoo, A.; Sander, V.; Talvik, T. (2003). A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia. European Journal of Paediatric Neurology, 7 (5), 221−226.
5.2.
2003
Ilves, P.; Lintrop, M.; Talvik, I. (2003). Herpes simplex virus 2 encephalitis in newborn infants. Eesti Arst, 83. 85.
1.1.
2002
Talkop, UA.; Talvik, I.; Sonajalg, M.; Sibul, H.; Kolk, A.; Piirsoo, A.; Warzok, R.; Wulff, K.; Wehnert, MS.; Talvik, T. (2002). Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy. Neuromuscular Disorders, 12 (9), 878−881.
1.3.
2002
Hämarik, M.; Napa, A.; Sibul, H.; Kahre, T.; Talvik, I.; Piirsoo, A.; Talvik, T. (2002). Spinaalne lihasatroofialapseeas. Ülevaade ja olukorra analüüs. Eesti Arst, 8, 488−492.
1.3.
2002
Talvik, I.; Vibo, R.; Metsvaht, T.; Männamaa, M.; Jüri, P.; Heidmets, L.; Hämarik, M.; Talvik, T. (2002). Raputatud lapse sündroom. Eesti Arst, 81 (1), 23−29.
5.2.
2002
Lintrop, M.; Ilves, P.; Järv, V.; Leht, M.; Talvik, I. (2002). Cranial ultrasound in the shaken baby syndrome. Materials of the 55th Radiological Congress; Reykjavik, Island.
1.3.
2001
Metsvaht, T.; Talvik, I.; Sillapere, P.; Paluste, M.; Kütt, E.; Sau, L.; Talvik, T.; Talvik, R. (2001). IgM-enriched intravenous immunoglobulin for the prevention of infections in low birth weight neonates. Focus Medicinae, 4, 17−27.
1.1.
2000
Talvik, I.; Ounap, K.; Bartsch, O.; Ilus, T.; Uibo, O.; Talvik, T. (2000). Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32 - > qter. American Journal of Medical Genetics, 93 (5), 399−402.
1.1.
2000
Salur, L.; Uibo, O.; Talvik, I.; Justus, I.; Metskula, K.; Talvik, T.; Uibo, R. (2000). The high frequency of coeliac disease among children with neurological disorders. European Journal of Neurology, 7 (6), 707−711.
1.1.
1999
Beilmann, A.; Napa, A.; Soot, A.; Talvik, I.; Talvik, T. (1999). Prevalence of childhood epilepsy in Estonia. Epilepsia, 40 (7), 1011−1019.
1.1.
1999
Beilmann, A.; Napa, A.; Hamarik, M.; Soot, A.; Talvik, I.; Talvik, T. (1999). Incidence of childhood epilepsy in Estonia. Brain & Development, 21 (3), 166−174.
1.2.
1995
Ilves, Pilvi; Kütt, Ever; Mägi, Marja-Liis; Kudrjavtseva, Galina; Talvik, Inga; Talvik, Tiina (1995). Cerebral blood flow in asphyxiated term newborns with hypoxic-ischaemic encephalopathy. Medicina, 31, 106.
5.1.
1995
Beilmann, A.; Soot, A.; Talvik, I.; Napa, A.; Talvik, T. (1995). Etiologic factors and short-term outcome of infantile spasms. Epilepsia, 36, S203−S203.
5.2.
0
Noormets, Klari; Talvik, Inga; Reimand, Tiia; Õiglane-Šlik, Eve; Õunap, Katrin; Talvik, Tiina (0). Copy number variants associated with drug-resistant epilepsy in Estonia. In: . Young Researchers in Epileptology Meeting 2013, 14. Dec 2013, Sde Boker, Israel.
25.05.2020

Inga Talvik

https://www.etis.ee/CV/Inga_Talvik/eng
6.05.1965
731 9580
inga.talvik@ut.ee
http://

Career

Institutions and positions
01.02.2019–31.12.2022   
University of Tartu, Faculty of Medicine, Institute of Clinical Medicine, Research Fellow of Paediatric Neurology (0,30)
2017–...   
Tallinn Children Hospital, Head of the departement of Neurology and rehabilitation (1,00)
01.01.2016–01.09.2017   
Tallinn Children Hospital, Neurologist (1,00)
01.09.2014–31.12.2015   
University of Tartu, Faculty of Medicine, Department of Pediatrics, Associate Professor in Paediatric Neurology (0,50)
01.09.2009–31.08.2014   
University of Tartu, Faculty of Medicine, Department of Pediatrics, Associate Professor in Paediatric Neurology (0,50)
01.09.2008–31.08.2009   
University of Tartu, Faculty of Medicine, Department of Pediatrics, Senior Assistant (0,50)
15.02.2008–31.05.2008   
University of Tartu, Faculty of Medicine, Department of Pediatrics, Specialist (0,30)
2008–2009   
University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics, lasteneuroloogia vanemassistent (0,50)
2005–31.12.2015   
Tartu University Hospital, Children's Clinic of Tartu University Hospital, senior doctor (1,00)
01.01.2005–31.12.2010   
Children`S Clinic of Tartu University Hospital
 
 
Education
1983–1989   
Tartu University Medical Faculty
1972–1983   
Tartu Secondary School no 2
 
 
R&D related managerial and administrative work
2013−...   
Estonian Pediatric Neurology Association - president
2009−...   
Estonian league against epilepsy
2006−...   
European Association of Pedaitric Neurology
2000−...   
Estonian Society of Human Genetics
2006−2015   
Eesti Epilepsia Liit - juhatuse esimees
 
 
Creative work
Huvitatud teadvustööst epilepsiast
 
 
Additional information
Neuroloog- lasteneuroloog

Qualifications

Academic degrees
Inga Talvik, Doctor's Degree, 2007, (sup) Tiina Talvik, Inflicted traumatic brain injury/shaken baby syndrome in Estonia- epidemiology and outcome, University of Tartu, Faculty of Medicine.
 
 

Projects in progress

Completed projects

Dissertations under supervision

Publications

Category
Year
Publication
 
1.1.
2017
Møller, Rikke S; Wuttke, Thomas V; Helbig, Ingo; Marini, Carla; Johannesen, Katrine M; Brilstra, Eva H; Vaher, Ulvi; Borggraefe, Ingo; Talvik, Inga; Talvik, Tiina; Kluger, Gerhard; Francois, Laurence L; Lesca, Gaetan; de Bellescize, Julitta; Blichfeldt, Susanne; Chatron, Nicolas; Holert, Nils; Jacobs, Julia; Swinkels, Marielle; Betzler, Cornelia ... Maljevic, Snezana (2017). Mutations in GABRB3: From febrile seizures to epileptic encephalopathies. Neurology, 88 (5), 483−492.10.1212/WNL.0000000000003565.
1.1.
2017
Ilves,Nigul; Ilves, PIlvi; Laugesaar, Rael; Juurmaa, Julius; Männamaa, Mairi; Lõo, Silva; Loorits, Dagmar; Tomberg, Tiiu; Kolk, Anneli; Talvik, Inga; Talvik, Tiina (2017). Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal Stroke. Neural Plasticity, 2016, 11−11. DOI: 10.1155/2016/2306406.
5.2.
2017
Ilves, Nigul; Ilves, Pilvi; Laugesaar, Rael; Juurmaa, Julius; Männamaa, Mairi; Lõo, Silva; Loorits, Dagmar; Tomberg, Tiiu; Kolk, Anneli; Talvik, Inga; Talvik, Tiina; (2017). Correlations in resting-state functional networks and cognitive functions in children with perinatal stroke and healthy controls. In: . European Congress of Magnetic Resonance in Neuropediatrics, Tübingen Germany, June 8 to 10, 2017.
1.1.
2016
Reinson, Karit; Õiglane-Shlik, Eve; Talvik, Inga; Vaher, Ulvi; Õunapuu, Anne; Ennok, Margus; Teek, Rita; Pajusalu, Sander; Murumets, Ülle; Tomberg, Tiiu; Puusepp, Sanna; Piirsoo, Andres; Reimand, Tiia; Õunap, Katrin (2016). Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. American Journal of Medical Genetics Part A, 170 (8), 2173−2176. DOI: 10.1002/ajmg.a.37678.
1.1.
2016
Lilles, Stella; Talvik, Inga; Noormets, Klari; Vaher, Ulvi; Õunap, Katrin; Reimand, Tiia; Sander, Valentin; Ilves, Pilvi; Talvik, Tiina (2016). CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature. Neuropediatrics, 47 (6), 361−367. DOI: 10.1055/s-0036-1586730.
1.1.
2016
Pajusalu, S.; Talvik, I.; Noormets, K.; Talvik, T.; Põder, H.; Joost, K.; Puusepp, S.; Piirsoo, A.; Stenzel, W.; Goebel, HH.; Nikopensius, T.; Annilo, T.; Nõukas, M.; Metspalu, A.; Õunap, K.; Reimand, T. (2016). De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion. Neuromuscular Disorders, 26 (3), 236−239. DOI: 10.1016/j.nmd.2015.11.011.
1.1.
2016
Johannesen, Katrine; Marini, Carla; Pfeffer, Siona; Møller, Rikke S; Dorn, Thomas; Niturad, Cristina Elena; Gardella, Elena; Weber, Yvonne; Søndergård, Marianne; Hjalgrim, Helle; Nikanorova, Mariana; Becker, Felicitas; Larsen, Line H G; Dahl, Hans A; Maier, Oliver; Mei, Davide; Biskup, Saskia; Klein, Karl M; Reif, Philipp S; Rosenow, Felix ... Maljevic, Snezana (2016). Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. Neurology, 87 (11), 1140−1151.10.1212/WNL.0000000000003087.
1.2.
2016
Møller, Rikke S; Larsen, Line H G; Johannesen, Katrine M; Talvik, Inga; Talvik, Tiina; Vaher, Ulvi; Miranda, Maria J; Farooq, Muhammad; Nielsen, Jens E K; Svendsen, Lene Lavard; Kjelgaard, Ditte B; Linnet, Karen M; Hao, Qin; Uldall, Peter; Frangu, Mimoza; Tommerup, Niels; Baig, Shahid M; Abdullah, Uzma; Born, Alfred P; Gellert, Pia ... Dahl, Hans A (2016). Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. Molecular Syndromology, 7 (4), 210−219.
5.2.
2016
J. Katus, I. Talvik, S. Margus, R. Laugesaar, D. Loorits, V. Tolpats, E. Õiglane-Šlik, T. Talvik, P. Ilves. (2016). 7-aastase poisi basilaartromboosi ravi intaarteriaalse trombektoomia abil - haigusjuhu kirjeldus. Eesti Lastearstide Seltsi XXI kongressi abstraktide kogumik (47).Eesti Lastearstide Seltsi XXI kongress, 2.-4. juuni 2016, Tallinn..
5.2.
2016
Jesse K, Laugesaar R, Lõo S, Ilves P, Kolk A, Talvik I, Talvik T. (2016). Gross motor function in children after perinatal ishemic stroke. In: International Conference on Cerebral Palsy and other Childhood-onset Disabilities 2016 Abstract Book. International Conference on Cerebral Palsy and other Childhood-onset Disabilities, Stockholm, 1–4 June 2016.
5.2.
2016
Katus Jaan, Talvik Inga, Laugesaar Rael, Õiglane-Šlik Eve, Margus Sulev, Loorits Dagmar, Talvik Tiina, Ilves Pilvi. (2016). Intraarterial thrombectomy in a previously healthy 7-years-old boy with basilar artery thrombosis. In: Baltic Congress of Radiology 2016 Abstract book (32−33).Baltic Congress of Radiology, October 6-8, 2016, Liepaja, Latvia.
5.2.
2016
R. Laugesaar, S. Lõo, U. Vaher, M. Männamaa, A. Kolk, I. Talvik, E. Õiglane-Šlik, V. Sander, D. Loorits, T. Tomberg, T. Talvik, P. Ilves. (2016). Epilepsia perinataalset insulti põdenud lastel. Eesti Lastearstide Seltsi XXI kongressi abstraktide raamat (30). Eesti Lastearstide Seltsi XXI kongress. 2.-4. juuni 2016, Tallinn..
5.2.
2016
N. Ilves, P. Ilves, R. Laugesaar, J. Juurmaa, S. Lõo, M. Männamaa, D. Loorits, T. Tomberg, A. Kolk, I. Talvik, T. Talvik. (2016). Erinevused rahuoleku funktsionaalses konnektiivsuses perinataalse arteriaalse isheemilise insuldi ja hilise diagnoosiga periventrikulaarse venoosse insuldiga lastel. Eesti Lastearstide Seltsi XXI Kongressi abstraktide kogumik (32). Eesti Lastearstide Seltsi XXI Kongress. 2.-4. juuni 2016, Tallinn..
1.1.
2014
Žilina, O.; Kahre, T.; Talvik, I.; Õiglane-Shlik, E.; Tillmann, V.; Õunap, K. (2014). Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome. European Journal of Medical Genetics, 57 (6), 279−283. DOI: 10.1016/j.ejmg.2014.03.007.
1.1.
2014
Õiglane-Shlik, E.; Puusepp, S.; Talvik, I.; Vaher, U.; Rein, R.; Tammur, P.; Reimand, T.; Teek, R.; Žilina, O.; Tomberg, T.; Õunap, K. (2014). Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities. European Journal of Paediatric Neurology, 18 (3), 338−346. DOI: 10.1016/j.ejpn.2014.01.008.
1.1.
2014
Vaher, Ulvi; Nõukas, Margit; Nikopensius, Tiit; Kals, Mart; Annilo, Tarmo; Nelis, Mari; Õunap, Katrin; Reimand, Tiia; Talvik, Inga; Ilves, Pilvi; Piirsoo, Andres; Seppet, Enn; Metspalu, Andres; Talvik, Tiina (2014). De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders. Journal of Child Neurology, 29 (12), 202−206. DOI: 10.1177/0883073813511300.
1.1.
2013
Suls, A.; Jaehn, JA.; Kecskés, A.; Weber, Y.; Weckhuysen, S.; Craiu, DC.; Siekierska, A.; Djémié, T.; Afrikanova, T.; Gormley, P.; von Spiczak, S.; Kluger, G.; Iliescu, CM.; Talvik, T.; Talvik, I.; Meral, C.; Caglayan, HS.; Giraldez, BG.; Serratosa, J.; Lemke, JR. ... Helbig, I. EuroEPINOMICS RES Consortium (2013). De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. The American Journal of Human Genetics, 93 (5), 967−975.10.1016/j.ajhg.2013.09.017.
1.1.
2013
Veri, K; Uibo, O; Talvik, T; Talvik, I; Metsküla, K; Napa, A; Vaher, U; Õiglane-Šlik, E; Rein, R; Kolk, A; Traat, A; Uibo, R. (2013). Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipin. Epilepsy Research, 105, 86−91.10.1016/j.eplepsyres.2013.02.009.
5.1.
2013
Tammur, P.; Reimand, T.; Žilina, O.; Talvik, I.; Ilisson, P.; Ilus, T.; Toit, P.; Kuuse, K.; Õunap, K. (2013). Copy-number variations at 16p11.2 in Estonian patients. European Journal of Human Genetics, 21: European Human Genetics Conference 2013; June 8 - 11, 2013; Palais des Congrès, Paris, France. Nature Publishing Group, 157−157.
5.2.
2013
Pajusalu, S.; Õiglane-Šlik, E.; Talvik, I.; Teek, R.; Žilina, O.; Kuuse, K.; Reimand, T.; Õunap, K. (2013). Clinical characterization of six patients with 15q13.2-q13.3 microdeletion. In: . First International GENCODYS Conference, Integrative Networks in Intellectual Disabilities; Paphos, Cyprus; 14-17 April 2013.
5.2.
2013
Noormets, Klari; Õunap, Katrin; Talvik, Tiina; Talvik, Inga (2013). CDKL5 gene related epileptic encephalopathy in Estonia: a case presentation. Seminars in Neurology: 12th Congress of the Baltic Child Neurology Association, Kaunas, Lithuania, 30 May - 01 June 2013. S45−S45.
1.1.
2012
Joost, K.; Rodenburg, R.J.; Piirsoo, A.; van den Heuvel, L.; Žordania, R.; Põder, H.; Talvik, I.; Kilk, K.; Soomets, U.; Õunap, K. (2012). A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children. Molecular Syndromology, 3 (3), 113−119.10.1159/000341375.
1.1.
2012
Tiigimäe-Saar, J.; Leibur, E.; Kolk, A.; Talvik, I.; Tamme, T. (2012). Use of Botulinum neurotoxin A in uncontrolled salivation in children with cerebral palsy. A pilot study. International Journal of Oral and Maxillofacial Surgery, 41 (12), 1540−1545.10.1016/j.ijom.2012.09.015.
1.1.
2012
Krabbi, K.; Joost, K.; Zordania, R.; Talvik, I.; Rein, R.; Huijmans, J. G. M.; Verheijen, F. V.; Õunap, K (2012). The live-birth prevalence of mucopolysaccharidoses in Estonia. Genetic Testing and Molecular Biomarkers, 16 (8), 846−849.10.1089/gtmb.2011.0307.
1.1.
2012
Talvik, I.; Vibo, R.; Liik, M.; Haldre, S.; Talvik, T. (2012). Epileptic laughter: 2 case reports. Medicina (Kaunas), 48 (7), 359−363.
1.3.
2012
Laugesaar, Rael; Pajusalu, Sander; Toome, Liis; Kolk, Anneli; Tomberg, Tiiu; Ilves, Pilvi; Eelmäe, Imbi; Talvik, Inga; Talvik, Tiina (2012). Sinovenoosne tromboos lastel: kirjanduse ülevaade ja kogemus Eestis [Paediatric cerebral sinovenous thrombosis in Estonia]. Eesti Arst, 91 (11), 604−609.
3.1.
2012
Talvik, Tiina; Kirkham, Fenella; Metsvaht, Tuuli; Talvik, Inga (2012). Principles and Practice of Child Neurology in Infancy. In: Colin Kennedy (Ed.). Principles and Practice of Child Neurology in Infancy (179−204).. Principles and Practice of Child Neurology in Infancy , Mac Keith Press, London UK 6 Market Road, London N7 9PW, UK : Wiley InterScience.
5.1.
2012
Kall, K.; Reimand, T.; Talvik, I.; Pop, A.; Salomons, GS.; Õunap, K. (2012). Biochemical diagnostics of creatine transporter deficiency in Estonia. JOURNAL OF INHERITED METABOLIC DISEASE, 35 (suppl 1): Annual Symposium of the Society for the Study of Inborn Errors of Metabolism; Birmingham, UK, 4 – 7 September 2012. Springer, S54−S54.
5.2.
2012
Mikkel, S.; Boriskina, K.; Talvik, I.; Reimand, T.; Everaus, H. (2012). Familiar hemophagocytic lymphohistiocytosis - case report. Abstract book 8th Baltic Conference on Hematology: 8th Baltic Conference on Hematology; 12-14.04.2012; Tallinn. , 77−78.
5.2.
2012
Uibo, O.; Veri, K.; Talvik, I.; Metsküla, K.; Traat, A.; Heilman, K.; Talvik, T.; Uibo, R. (2012). Autoantibodies to glutamic acid decarboxylase in children with newly-diagnosed epilepsy: rare association with type i diabetes. Abstracts.: 12th International Conference on the Immunology of Diabetes; Victoria, Kanada; 15-19.06.2012. , 151−152.
5.2.
2012
Laugesaar, R.; Pajusalu, S.; Toome, L.; Kolk, A.; Tomberg, T.; Ilves, P.; Eelmäe, I.; Talvik, I.; Talvik, T. (2012). Paediatric cerebral sinovenous thrombosis in Estonia. Abstract book: The 7th Baltic Congress of Neurology, Tartu, Estonia, May 9-12, 2012. 162.
1.1.
2011
Joost, K.; Tammur, P.; Teek, R.; Žilina, O.; Peters, M.; Kreile, M.; Lace, B.; Žordania, R.; Talvik, I.; Õunap, K. (2011). Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency. Molecular Syndromology, 1 (6), 311−315. DOI: 10.1159/000331323.
3.3.
2011
Metsvaht, Tuuli; Vainumäe, Inga; Gontmacher, Aasa; Grünberg, Heli; Eelmäe, Imbi; Maipuu, Lea; Tamm, Eda; Torm, Siiri; Pütsepp, Aime; Sizarov, Aleksandr; Laan, Mari; Virro, Silvia; Varendi, Heili; Veinla, Maie; Mägi, Marja-Liis; Külasepp, Piret; Kallas, Eha; Talvik, Inga; Kolk, Anneli; Talvik, Tiina ... Kõrgvee, Lenne-Triin (2011). Valvearsti teatmik [Reference book for doctors on call]. Heli Grünberg (Toim.). Valvearsti teatmik. . Tartu: Tartu University Press.
5.2.
2011
Reimand, T.; Uibo, O.; Luts, K.; Talvik, I.; Zhilina, O.; Muru, K.; Õunap, K. (2011). Microdeletion 10q23 and juvenile polyposis syndrome: a case report. European Human GenetiConference cs 2011, Amsterdam RAI, The Netherlands, May 28 - 31, 2011. x, x.
5.2.
2011
Tammur, P.; Reimand, T.; Õiglane-Šlik, E.; Teek, R.; Zilina, O.; Talvik, I.; Ilisson, P.; Ilus, T.; Kuuse, K.; Jürgenson, M.; Õunap, K. (2011). Four cases of 1p36 microdeletion and their clinical characterization. 8th European Cytogenetics Conference, Porto, Portugal, July 2-5, 2011.
1.1.
2010
Talvik, I.; Segawa, M.; Veri, K.; Gross-Paju, K.; Talvik, T. (2010). Cases of dopa-responsive dystonia (Segawa disease) in Estonia. Brain Dev, 32 (5), 428−431.10.1016/j.braindev.2009.04.007.
1.1.
2010
Talvik, Inga; Peet, Aleksandr; Laugesaar, Rael; Lintrop, Mare; Talvik, Tiina (2010). Vehicle-associated closed trauma-induced stroke in a 27-day-old girl. Medicina (Kaunas), 624−627.
1.1.
2010
Ilves, Pilvi; Lintrop, Mare; Talvik, Inga; Sisko, Annika; Talvik, Tiina (2010). Predictive value of clinical and radiological findings in inflicted traumatic brain injury. Acta Paediatrica, 99 (9), 1329−1336.10.1111/j.1651-2227.2010.01820.x.
1.1.
2010
Laugesaar, R.; Kolk, A.; Uustalu, Ü.; Ilves, P.; Tomberg, T.; Talvik, I.; Köbas, K.; Sander, V.; Talvik, T. (2010). Epidemiology of childhood stroke in Estonia. Pediatric Neurology, 42 (2), 93−100.
1.3.
2010
Lintrop, Mare; Talvik, Inga; Tolpats, Viive; Nellis, Georgi; Mikkel, Sirje; Padari, Helgi; Napa, Aita; Ilves, Pilvi (2010). Posterioorse reversiibelse entsefalopaatia sündroom (PRES): kirjanduse ülevaade ja kahe haigusjuhu kirjeldus [Posterior reversible encephalopathy syndrome (PRES): a literature overview and two case reports]. Eesti Arst, 89 (3), 191−199.
1.3.
2010
Inga Talvik, Reili Rebane, Tiia Reimand, Aita Napa, Tiina Talvik (2010). Ravile raskesti alluv epilepsia 20. rõngaskromosoomi sündroomi korral: kirjanduse ülevaade ja haigusjuhu kirjeldus [Intractable epilepsy in the case of ring 20 chromosome syndrome: overview and a case description]. Eesti Arst, 89 (10), 646−650.
5.2.
2010
Reimand, T.; Uibo, O.; Luts, K.; Talvik, I.; Zilina, O.; Muru, K.; Õunap, K. (2010). Mikrodeletsioon 10q23.1-q23.3 juveniilse polüpoosi põhjusena. (45−45). Eesti Lastearstide 19.kongress.
5.2.
2010
Veri, K.; Uibo, O.; Metsküla, K.; Talvik, I.; Napa, A.; Vaher, U.; Rein, R.; Õiglane-Slik, E.; Kolk, A.; Talvik, T.; Uibo, R. (2010). Autoantikehade esinemine epilepsia diagnoosiga lastel. (20−20). Eesti Lastearstide 19.kongress.
5.2.
2010
Ilves, Pilvi; Lintrop, Mare; Talvik, Inga; Sisko, Annika (2010). Correlations between late radiological findings and long-term neurodevelopmental outcome in inflicted traumatic brain injury. Pediatric Radiology, 40: ESPR 2010; Bordeaux, France; 7-10 June 2010. Springer, 1076.
5.2.
2010
Lintrop, Mare; Ilves, Pilvi; Tolpats, Viive; Talvik, Inga (2010). Posterior reversible encephalopathy syndrome: two cases in children. Pediatric Radiology: ESPR 2010; Bordeaux, France; 7-10 June. Springer, 1116.
5.2.
2010
Vainumäe, I.; Rägo, T.; Metsvaht, T.; Mikkel, S.; Talvik, I.; Vals, M.-A.; Luts, K.; Kahre, T. (2010). Wilsoni tõbi lastel. 1996–2009 TÜ Kliinikumi lastekliinikus diagnoositud juhud. Eesti Arst, 89: Eesti lastearstide 19. kongress 3.-5.-06.2010. Tallinn, 62−62. (lisa 1).
1.1.
2009
Ilves, P.; Lintrop, M.; Talvik, I.; Muug, K.I; Maipuu, L. (2009). Changes in cerebral and visceral blood flow velocities in asphyxiated term infants with hypoxic ischemic encephalopathy. Journal of Ultrasound in Medicine, 28 (11), 1471−1480.
1.1.
2009
Talvik, I.; Peet, A.; Talvik, T. (2009). Three-year follow-up of a girl with chronic paroxysmal hemicrania. Pediatric Neurology, 1, 68−69.
1.1.
2009
Ilves, P.; Lintrop, M.; Talvik, I.; Muug, K.; Maipuu, L.; Metsvaht, T. (2009). Low cerebral blood flow velocity and head circumference in infants with severe hypoxic ischemic encephalopathy and poor outcome. Acta Paediatrica, 98 (3), 459−465. DOI: 10.1111/j.1651-2227.2008.01119.x.
6.7.
2009
Talvik, Inga; Väli, Marika; Mirka, Gerli; Ilves, Pilvi; Lintrop, Mare; Sisko, Annika; Kolk, Anneli; Talvik, Tiina; Alexander, Randell (2009). X International Conference of Baltic Child Neurology Association (BCNA), Tartu, Estonia, may 6-9, 2009 [Videosalvestis] : Session III: Traumatic brain injury. International Conference of Baltic Child Neurology Association(10 :2009 :Tartu). Tartu: TÜ IT Õppetehnika talitus. (TÜ filmiarhiiv).
1.1.
2008
Ilves, Pilvi; Lintrop, Mare; Talvik, Inga; Muug, Külli; Asser, Karin; Veinla, Maie (2008). Developmental changes in cerebral and visceral blood flow velocity in healthy neonates and infants [Aju ja vistseraalsete verevoolukiiruste arengulised muutused tervetel vastsündinutel ja imikutel]. Journal of Ultrasound in Medicine, 27 (2), 199−207.
1.1.
2008
Talvik, I.; Alexander, R.; Talvik, T. (2008). Shaken baby syndrome and a baby's cry. Acta Paediatrica, 97 (6), 782-−785.
1.1.
2008
Ventsel, G.; Kolk, A.; Talvik, I.; Väli, M.; Vaikmaa, M.; Talvik, T. (2008). The Incidence of Childhood Traumatic Brain Injury in Tartu and Tartu County in Estonia. Neuroepidemiology, 30 (1), 20−24. DOI: 10.1159/000113302.
1.1.
2007
Vaidla, E.; Talvik, I.; Kulla, A.; Sibul, H.; Maasalu, K.; Metsvaht, T.; Piirsoo, A.; Talvik, T. (2007). Neonatal spinal muscular atrophy type 1 with bone fractures and heart defect. Journal of Child Neurology, 22 (1), 67−70. DOI: 10.1177/0883073807299954.
1.1.
2007
Talvik, I.; Männamaa, M.; Jüri, P.; Leito, K.; Põder, H.; Hämarik, M.; Kool, P.; Talvik, T. (2007). Outcome of infants with inflicted traumatic brain injury (Shaken baby Syndrome) in Estonia. Acta Paediatrica, 96 (8), 1164−1168. DOI: 10.1111/j.1651-2227.2007.00362.x.
1.3.
2007
Talvik, I.; Lintrop, M.; Metsvaht, T.; Talvik, T. (2007). Millal mõelda raputatud lapse sündroomile: kirjanduse ülevaade ning haigusjuhu kirjeldus [When should one think about inflicted brain injury: a literature overview and a case report]. Eesti Arst, 86 (6), 420−423.
1.3.
2007
Talvik, I.; Koch, K.; Talvik, T. (2007). Krooniline paroksüsmaalne hemikraania: kirjanduse ülevaade ja 3 aasta 10 kuu vanuse tütarlapse edukas ravitulemus indometatsiiiniga. Eesti Arst, 86 (8), 517−520.
2.3.
2007
Talvik, I. (2007). Inflicted traumatic brain injury / shaken baby syndrome in Estonia - epidemiology and outcome. (Tartu Ülikool). Tartu University Press.
1.1.
2006
Talvik, I.; Koch, K.; Kolk, A.; Talvik, T. (2006). Chronic paroxysmal hemicrania in 3-year 10 month-old female. Pediatric Neurology, 34 (3), 225−227.
1.1.
2006
Vaidla , E.; Talvik, I.; Kulla, A.; Kahre, T.; Hämarik, M.; Napa , A.; Metsvaht, T.; Piirsoo, A.; Talvik , T. (2006). Descriptive epidemiology of spinal muscular atrophy type I in Estonia. Neuroepidemiology, 27 (3), 164−168.
1.1.
2006
Talvik, I.; Metsvaht, T.; Leito, K.; Põder, H.; Kool, P.; Väli, M.; Lintrop, M.; Kolk, A.; Talvik, T. (2006). Inflicted traumatic brain injury (ITBI) or shaken baby syndrome (SBS) in Estonia. Acta Paediatrica, 95 (7), 799−804. DOI: 10.1080/08035250500464923.
1.3.
2006
Talvik, I.; Veri, K.; Gross-Paju, K.; Kolk, A.; Talvik, T. (2006). Dopamiintundlik düstoonia: kirjanduse ülevaade ja haigusjuhu kirjeldus. Eesti Arst, 85 (12), 841−844.
5.2.
2004
Lintrop, Mare; Ilves, Pilvi; Talvik, Inga (2004). Aju ultraheliuuringud raputatud lapse diagnostikas. Eesti Arst, 83 (5), 336.
1.1.
2003
Talkop, U.A.; Kahre, T.; Napa, A.; Talvik, I.; Soot, A.; Piirsoo, A.; Sander, V.; Talvik, T. (2003). A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia. European Journal of Paediatric Neurology, 7 (5), 221−226.
5.2.
2003
Ilves, P.; Lintrop, M.; Talvik, I. (2003). Herpes simplex virus 2 encephalitis in newborn infants. Eesti Arst, 83. 85.
1.1.
2002
Talkop, UA.; Talvik, I.; Sonajalg, M.; Sibul, H.; Kolk, A.; Piirsoo, A.; Warzok, R.; Wulff, K.; Wehnert, MS.; Talvik, T. (2002). Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy. Neuromuscular Disorders, 12 (9), 878−881.
1.3.
2002
Hämarik, M.; Napa, A.; Sibul, H.; Kahre, T.; Talvik, I.; Piirsoo, A.; Talvik, T. (2002). Spinaalne lihasatroofialapseeas. Ülevaade ja olukorra analüüs. Eesti Arst, 8, 488−492.
1.3.
2002
Talvik, I.; Vibo, R.; Metsvaht, T.; Männamaa, M.; Jüri, P.; Heidmets, L.; Hämarik, M.; Talvik, T. (2002). Raputatud lapse sündroom. Eesti Arst, 81 (1), 23−29.
5.2.
2002
Lintrop, M.; Ilves, P.; Järv, V.; Leht, M.; Talvik, I. (2002). Cranial ultrasound in the shaken baby syndrome. Materials of the 55th Radiological Congress; Reykjavik, Island.
1.3.
2001
Metsvaht, T.; Talvik, I.; Sillapere, P.; Paluste, M.; Kütt, E.; Sau, L.; Talvik, T.; Talvik, R. (2001). IgM-enriched intravenous immunoglobulin for the prevention of infections in low birth weight neonates. Focus Medicinae, 4, 17−27.
1.1.
2000
Talvik, I.; Ounap, K.; Bartsch, O.; Ilus, T.; Uibo, O.; Talvik, T. (2000). Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32 - > qter. American Journal of Medical Genetics, 93 (5), 399−402.
1.1.
2000
Salur, L.; Uibo, O.; Talvik, I.; Justus, I.; Metskula, K.; Talvik, T.; Uibo, R. (2000). The high frequency of coeliac disease among children with neurological disorders. European Journal of Neurology, 7 (6), 707−711.
1.1.
1999
Beilmann, A.; Napa, A.; Soot, A.; Talvik, I.; Talvik, T. (1999). Prevalence of childhood epilepsy in Estonia. Epilepsia, 40 (7), 1011−1019.
1.1.
1999
Beilmann, A.; Napa, A.; Hamarik, M.; Soot, A.; Talvik, I.; Talvik, T. (1999). Incidence of childhood epilepsy in Estonia. Brain & Development, 21 (3), 166−174.
1.2.
1995
Ilves, Pilvi; Kütt, Ever; Mägi, Marja-Liis; Kudrjavtseva, Galina; Talvik, Inga; Talvik, Tiina (1995). Cerebral blood flow in asphyxiated term newborns with hypoxic-ischaemic encephalopathy. Medicina, 31, 106.
5.1.
1995
Beilmann, A.; Soot, A.; Talvik, I.; Napa, A.; Talvik, T. (1995). Etiologic factors and short-term outcome of infantile spasms. Epilepsia, 36, S203−S203.
5.2.
0
Noormets, Klari; Talvik, Inga; Reimand, Tiia; Õiglane-Šlik, Eve; Õunap, Katrin; Talvik, Tiina (0). Copy number variants associated with drug-resistant epilepsy in Estonia. In: . Young Researchers in Epileptology Meeting 2013, 14. Dec 2013, Sde Boker, Israel.
25.05.2020

Otsi projekti

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Uus Frascati (2015)
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ProgrammLiikNumberNimiProjekti algusProjekti lõppVastutav täitjaAsutusFinantseerijapoolne rahastamine
ETFETF6627Ajutrauma lapseeas - epidemioloogiline uuring01.01.200631.12.2009Tiina TalvikTartu Ülikool; Tartu Ülikool, Arstiteaduskond46 307,83 EUR
MUUSARLA11091EEUROCORES/ EuroEPINOMICS01.06.201131.05.2014Tiina TalvikTartu Ülikool; Tartu Ülikool, Arstiteaduskond, Lastekliinik143 801,00 EUR
MUU602962GAbapentin in Paediatric Pain – GAPP01.01.201431.12.2018Inga TalvikSA Tartu Ülikooli Kliinikum48 005,74 EUR
ETFETF9325Intravenoosse fenobarbitaali ja lidokaiini farmakokineetika ajalistel hüpotermias vastsündinutel01.01.201231.12.2014Lenne-Triin KõrgveeTartu Ülikool, Arstiteaduskond43 200,00 EUR
SFSF0182695s05Lapse arengut ja krooniliste haiguste patogeneesi määravad varajased tegurid ja sellest tulenevad uued võimalused nende mõjutamiseks ja raviks.01.01.200531.12.2010Vallo TillmannTartu Ülikool, Arstiteaduskond577 556,01 EUR
SFSF0180004s11Lapse arengut, krooniliste haiguste patogeneesi, diagnoosimist ja ravi kaugtulemusi määravad tegurid lastel: uued võimalused nende mõjutamiseks ja raviks. 01.01.201131.12.2016Vallo TillmannTartu Ülikool; Tartu Ülikool, Meditsiiniteaduste valdkond, kliinilise meditsiini instituut830 340,00 EUR
PSGPSG297Ravimresistentne epilepsia lapseeas: haigestumus, levimus, struktuur ja etioloogia Eestis01.01.201931.12.2022Klari HeidmetsTartu Ülikool, Meditsiiniteaduste valdkond, kliinilise meditsiini instituut180 875,00 EUR
1.1.7.4.TA/4118Varajase lapsepõlve interdistsiplinaarse neuroteaduse uurimisrühma käivitamine01.01.201831.12.2020Mari-Liis KaldojaTallinna Ülikool22 350,00 EUR