Publications by authors named "Inga Talvik"

43Publications

Correction: The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 Aug;21(8):1896

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013 Paris, France.

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http://dx.doi.org/10.1038/s41436-018-0325-9DOI Listing
August 2019

Long-term neurodevelopmental outcome after perinatal arterial ischemic stroke and periventricular venous infarction.

Eur J Paediatr Neurol 2018 Nov 21;22(6):1006-1015. Epub 2018 Jul 21.

Children's Hospital, Pediatric Research Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

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https://linkinghub.elsevier.com/retrieve/pii/S10903798163029
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http://dx.doi.org/10.1016/j.ejpn.2018.07.005DOI Listing
November 2018

Correction to: The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 Jul;21(7):1671

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France.

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http://dx.doi.org/10.1038/s41436-018-0284-1DOI Listing
July 2019

The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 02 10;21(2):398-408. Epub 2018 Aug 10.

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France.

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http://www.nature.com/articles/s41436-018-0060-2
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http://dx.doi.org/10.1038/s41436-018-0060-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292495PMC
February 2019

Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia.

Mol Genet Metab Rep 2018 Jun 15;15:80-89. Epub 2018 Mar 15.

Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, 2 L. Puusepa Street, Tartu 51014, Estonia.

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http://dx.doi.org/10.1016/j.ymgmr.2018.03.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043467PMC
June 2018

Incidence of Childhood Epilepsy in Estonia.

J Child Neurol 2018 08 4;33(9):587-592. Epub 2018 Jun 4.

1 Department of Pediatrics, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1177/0883073818776760DOI Listing
August 2018

Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal Stroke.

Neural Plast 2016 15;2016:2306406. Epub 2016 Dec 15.

Department of Pediatrics, University of Tartu, Tartu, Estonia; Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1155/2016/2306406DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198182PMC
October 2017

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

Neurology 2017 01 4;88(5):483-492. Epub 2017 Jan 4.

From the Danish Epilepsy Centre (R.S.M., K.M.J., M.N.), Dianalund; Institute for Regional Health Services (R.S.M., K.M.J., M.N.), University of Southern Denmark, Odense; Department of Neurology and Epileptology (T.V.W., S.V., H.L., S.M.), Hertie Institute for Clinical Brain Research, and Department of Neurosurgery (T.V.W.), University of Tübingen; Department of Neuropediatrics (I.H., M.P., S.v.S., H.M.), University Medical Center Schleswig-Holstein, Kiel, Germany; Division of Neurology (I.H., S.H., H.D.), The Children's Hospital of Philadelphia, PA; Neuroscience Department (C.M., R.G.), Children's Hospital Anna Meyer-University of Florence, Italy; Department of Genetics (E.H.B., M.S., K.L.v.G.), University Medical Center Utrecht, the Netherlands; Department of Neurology and Neurorehabilitation (U.V., I.T., T.T.), Children's Clinic of Tartu University Hospital, Estonia; Department of Pediatric Neurology and Epilepsy Center (I.B.), LMU Munich, Germany; Department of Pediatrics (I.T., T.T.), University of Tartu; Tallinn Children's Hospital (I.T.), Tallinn, Estonia; Clinic for Neuropediatrics and Neurorehabilitation (G.K., C.B., H.H.), Epilepsy Center for Children and Adolescents, Schön Klinik Vogtareuth, Germany; Paracelsus Medical Private University (G.K.), Salzburg, Austria; Neuropeadiatric Department (L.L.F.), Hospices Civils de Lyon; Department of Genetics (G.L., N.C.), Lyon University Hospitals; Claude Bernard Lyon I University (G.L., N.C.); Lyon Neuroscience Research Centre (G.L., N.C.), CNRS UMR5292, INSERM U1028; Epilepsy, Sleep and Pediatric Neurophysiology Department (J.d.B.), Lyon University Hospitals, France; Clinic for Pediatric Neurology (S.B.), Pediatric Department, University Hospital, Herlev, Denmark; Kleinwachau (N.H.), Sächsisches Epilepsiezentrum Radeberg, Dresden; Department of Neuropediatrics/Epilepsy Center (J.J.), University Medical Center Freiburg; Department of General Paediatrics (S.S.), Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg; Department of Women and Child Health (S.S.), Hospital for Children and Adolescents, University of Leipzig Hospitals and Clinics, Germany; Department of Pediatrics (C.T.M., H.C.M.), Division of Genetic Medicine, University of Washington, Seattle; Amplexa Genetics (L.H.G.L., H.A.D.), Odense, Denmark; Northern German Epilepsy Center for Children and Adolescents (S.v.S.), Schwentinental-Raisdorf, Germany; Wilhelm Johannsen Centre for Functional Genome Research (Y.M., N.T.), Department of Cellular and Molecular Medicine, University of Copenhagen; Danish Epilepsy Center (G.R.), Filadelfia/University of Copenhagen, Denmark; Department of Diagnostics (J.R.L.), Institute of Human Genetics, University of Leipzig; and Svt. Luka's Institute of Child Neurology and Epilepsy (K.M.), Moscow, Russia. Dr Maljevic is currently at the Florey Institute of Neuroscience and Mental Health, Melbourne, Australia.

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http://dx.doi.org/10.1212/WNL.0000000000003565DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278942PMC
January 2017

CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature.

Neuropediatrics 2016 Dec 6;47(6):361-367. Epub 2016 Sep 6.

Department of Neurology and Neurorehabilitation, Children's Clinic, Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1055/s-0036-1586730DOI Listing
December 2016

De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion.

Neuromuscul Disord 2016 Mar 3;26(3):236-9. Epub 2015 Dec 3.

Department of Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia; Institute of Biomedicine and Translational Medicine, Department of Biomedicine, University of Tartu, Tartu, Estonia; Department of Pediatrics, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.nmd.2015.11.011DOI Listing
March 2016

Presumed Perinatal Stroke: Risk Factors, Clinical and Radiological Findings.

J Child Neurol 2016 Apr 7;31(5):621-8. Epub 2015 Oct 7.

Department of Pediatrics, University of Tartu, Tartu, Estonia Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1177/0883073815609149DOI Listing
April 2016

Clinical Phenotype of De Novo Mutation: Case Report and Review of Literature.

Child Neurol Open 2015 Apr-Jun;2(2):2329048X15583717. Epub 2015 May 5.

Department of Pediatrics, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1177/2329048X15583717DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417033PMC
May 2015

De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis.

Eur J Med Genet 2015 Jun-Jul;58(6-7):336-40. Epub 2015 Apr 20.

Department of Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia; Department of Paediatrics, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.ejmg.2015.04.002DOI Listing
March 2016

Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.

Eur J Med Genet 2014 May-Jun;57(6):279-83. Epub 2014 Apr 2.

Department of Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia; Department of Pediatrics, University of Tartu, Tartu, Estonia. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2014.03.007DOI Listing
February 2015

Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities.

Eur J Paediatr Neurol 2014 May 25;18(3):338-46. Epub 2014 Jan 25.

Department of Pediatrics, Faculty of Medicine, University of Tartu, Tartu, Estonia; Department of Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.ejpn.2014.01.008DOI Listing
May 2014

Valproic acid-induced pancreatitis in a 15-year-old boy with juvenile myoclonic epilepsy.

Medicina (Kaunas) 2013 ;49(11):487-9

Department of Pediatrics, University of Tartu, Lunini 6, 51014 Tartu, Estonia.

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December 2014

Epileptic laughter: 2 case reports.

Medicina (Kaunas) 2012 ;48(7):359-63

Children’s Clinic, Tartu University Hospital, University of Tartu, L. Puusepa str. 8, 51014 Tartu, Estonia.

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September 2013

The live-birth prevalence of mucopolysaccharidoses in Estonia.

Genet Test Mol Biomarkers 2012 Aug 5;16(8):846-9. Epub 2012 Apr 5.

Institute of Chemistry, Faculty of Sciences, Tallinn University of Technology, Tallinn, Estonia.

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http://www.liebertpub.com/doi/10.1089/gtmb.2011.0307
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http://dx.doi.org/10.1089/gtmb.2011.0307DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422553PMC
August 2012

Vehicle-associated closed trauma-induced stroke in a 27-day-old girl.

Medicina (Kaunas) 2010 ;46(9):624-7

Department of Neurology and Neurorehabilitation, Children's Clinic, Tartu University Hospital, Tartu, Estonia.

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June 2011

Predictive value of clinical and radiological findings in inflicted traumatic brain injury.

Acta Paediatr 2010 Sep;99(9):1329-36

Radiology Clinic, Tartu University Hospital, Tartu, Estonia.

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http://doi.wiley.com/10.1111/j.1651-2227.2010.01820.x
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http://dx.doi.org/10.1111/j.1651-2227.2010.01820.xDOI Listing
September 2010

Epidemiology of childhood stroke in Estonia.

Pediatr Neurol 2010 Feb;42(2):93-100

Department of Pediatrics, University of Tartu, Tartu, Estonia.

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https://linkinghub.elsevier.com/retrieve/pii/S08878994090040
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http://dx.doi.org/10.1016/j.pediatrneurol.2009.08.009DOI Listing
February 2010

Changes in cerebral and visceral blood flow velocities in asphyxiated term neonates with hypoxic-ischemic encephalopathy.

J Ultrasound Med 2009 Nov;28(11):1471-80

Department of Radiology, University of Tartu, Puusepa 2, 51014 Tartu, Estonia.

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http://www.jultrasoundmed.org/content/28/11/1471.full.pdf
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http://dx.doi.org/10.7863/jum.2009.28.11.1471DOI Listing
November 2009

Cases of dopa-responsive dystonia (Segawa disease) in Estonia.

Brain Dev 2010 May 7;32(5):428-31. Epub 2009 May 7.

Children's Clinic of Tartu University Hospital, Department of Paediatrics of Tartu University, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.braindev.2009.04.007DOI Listing
May 2010

Three-year follow-up of a girl with chronic paroxysmal hemicrania.

Pediatr Neurol 2009 Jan;40(1):68-9

Children's Clinic, Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.pediatrneurol.2008.10.002DOI Listing
January 2009

Low cerebral blood flow velocity and head circumference in infants with severe hypoxic ischemic encephalopathy and poor outcome.

Acta Paediatr 2009 Mar 11;98(3):459-65. Epub 2008 Nov 11.

Radiology Service, Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1111/j.1651-2227.2008.01119.xDOI Listing
March 2009

Shaken baby syndrome and a baby's cry.

Acta Paediatr 2008 Jun 7;97(6):782-5. Epub 2008 Apr 7.

Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1111/j.1651-2227.2008.00778.xDOI Listing
June 2008

The incidence of childhood traumatic brain injury in Tartu and Tartu County in Estonia.

Neuroepidemiology 2008 17;30(1):20-4. Epub 2008 Jan 17.

Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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https://www.karger.com/Article/FullText/113302
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http://dx.doi.org/10.1159/000113302DOI Listing
March 2008

Developmental changes in cerebral and visceral blood flow velocity in healthy neonates and infants.

J Ultrasound Med 2008 Feb;27(2):199-207

Radiology Service, Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.7863/jum.2008.27.2.199DOI Listing
February 2008

Neonatal spinal muscular atrophy type 1 with bone fractures and heart defect.

J Child Neurol 2007 Jan;22(1):67-70

Department of Pediatrics, Tartu University, 6 Lunini Street, Tartu 51014, Estonia.

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http://dx.doi.org/10.1177/0883073807299954DOI Listing
January 2007

Outcome of infants with inflicted traumatic brain injury (shaken baby syndrome) in Estonia.

Acta Paediatr 2007 Aug 18;96(8):1164-8. Epub 2007 Jun 18.

Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1111/j.1651-2227.2007.00362.xDOI Listing
August 2007

Descriptive epidemiology of spinal muscular atrophy type I in Estonia.

Neuroepidemiology 2006 ;27(3):164-8

Department of Paediatrics, Tartu University, Tartu, Estonia.

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http://dx.doi.org/10.1159/000096128DOI Listing
December 2006

Chronic paroxysmal hemicrania in a 3-year, 10-month-old female.

Pediatr Neurol 2006 Mar;34(3):225-7

Pediatric Neurology Unit, Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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http://linkinghub.elsevier.com/retrieve/pii/S088789940500504
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http://dx.doi.org/10.1016/j.pediatrneurol.2005.08.026DOI Listing
March 2006

A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia.

Eur J Paediatr Neurol 2003 ;7(5):221-6

Department of Paediatrics, Tartu University, 6 Lunini Street, Tartu 51014, Estonia.

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http://dx.doi.org/10.1016/s1090-3798(03)00077-1DOI Listing
December 2003

Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy.

Neuromuscul Disord 2002 Nov;12(9):878-81

Department of Pediatrics, Tartu University,6 Lunini Street, 51014, Tartu, Estonia.

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http://dx.doi.org/10.1016/s0960-8966(02)00134-7DOI Listing
November 2002