I. Talvik

O. Žilina, P. Tammur, T. Reimand, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Descriptive Epidemiology of Spinal Muscular Atrophy Type I in Estonia

I. Talvik, T. Metsvaht, T. Talvik, 2006, Neuroepidemiology.

The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia

S. Pajusalu, K. Õunap, I. Talvik, 2021, Frontiers in Genetics.

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

A. Peet, I. Talvik, T. Talvik, 2009, Pediatric neurology.

Shaken baby syndrome and a baby's cry

I. Talvik, T. Talvik, R. Alexander, 2008, Acta paediatrica.

Inflicted traumatic brain injury (ITBI) or shaken baby syndrome (SBS) in Estonia.

M. Väli, I. Talvik, T. Metsvaht, 2006, Acta paediatrica.

Neonatal Spinal Muscular Atrophy Type 1 With Bone Fractures and Heart Defect

I. Talvik, T. Metsvaht, T. Talvik, 2007, Journal of child neurology.

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

I. Talvik, T. Talvik, M. Männamaa, 2007, Acta paediatrica.

Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

N. Tommerup, G. Rubboli, R. Møller, 2016, Molecular Syndromology.

Use of botulinum neurotoxin A in uncontrolled salivation in children with cerebral palsy: a pilot study.

I. Talvik, E. Leibur, A. Kolk, 2012, International journal of oral and maxillofacial surgery.

Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency

O. Žilina, P. Tammur, K. Õunap, 2011, Molecular Syndromology.

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

R. Rodenburg, S. Pajusalu, K. Õunap, 2018, Molecular genetics and metabolism reports.

De novo variants in neurodevelopmental disorders with epilepsy

M. Daly, P. May, Sitao Wu, 2018, Nature Genetics.

Compound heterozygous SPATA 5 variants in four families and functional studies of SPATA 5 de fi ciency

T. Meitinger, T. Strom, R. Rodenburg, 2019 .

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

V. Tillmann, O. Žilina, K. Õunap, 2014, European journal of medical genetics.

Presumed Perinatal Stroke

P. Ilves, I. Talvik, T. Talvik, 2016, Journal of child neurology.

Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study

M. Jaatun, K. Katanyuwong, P. Kwan, 2018, Epilepsia open.

Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)

M. Jaatun, K. Katanyuwong, E. Pataraia, 2021, Orphanet Journal of Rare Diseases.

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

Ellen F. Macnamara, Ryan K. Dale, Pedro P. Rocha, 2021, Science Advances.

Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy

S. Pajusalu, T. Reimand, K. Õunap, 2016, American journal of medical genetics. Part A.

Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiency

T. Meitinger, T. Strom, R. Rodenburg, 2018, European Journal of Human Genetics.

The live-birth prevalence of mucopolysaccharidoses in Estonia.

K. Õunap, I. Talvik, R. Žordania, 2012, Genetic testing and molecular biomarkers.

Changes in Cerebral and Visceral Blood Flow Velocities in Asphyxiated Term Neonates With Hypoxic‐Ischemic Encephalopathy

P. Ilves, I. Talvik, M. Lintrop, 2009, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Trait impulsivity in Juvenile Myoclonic Epilepsy

P. Striano, M. Richardson, K. Hamandi, 2020, Annals of clinical and translational neurology.

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

I. Talvik, T. Talvik, K. Wulff, 2002, Neuromuscular Disorders.

Short case report Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy

I. Talvik, T. Talvik, K. Wulff, 2002 .

Incidence of childhood epilepsy in Estonia

I. Talvik, T. Talvik, A. Sööt, 1999, Brain and Development.

SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy

P. Striano, S. Topp, K. Hamandi, 2022, medRxiv.

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

L. Haataja, P. Ilves, I. Talvik, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Epidemiology of childhood stroke in Estonia.

P. Ilves, I. Talvik, T. Talvik, 2010, Pediatric neurology.

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

A. Peet, I. Talvik, T. Talvik, 2010, Medicina.

Epilepsy after perinatal stroke with different vascular subtypes

P. Ilves, I. Talvik, T. Talvik, 2018, Epilepsia open.

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

P. Ilves, I. Talvik, T. Talvik, 2016, Neural plasticity.

Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipin

R. Uibo, I. Talvik, Eve Õiglane-Šlik, 2013, Epilepsy Research.

TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study

M. Jaatun, K. Katanyuwong, E. Pataraia, 2018, Orphanet Journal of Rare Diseases.

Variation in prognosis and treatment outcome in juvenile myoclonic epilepsy: a Biology of Juvenile Myoclonic Epilepsy Consortium proposal for a practical definition and stratified medicine classifications

P. Striano, M. Richardson, M. Reuber, 2023, Brain communications.

Inflicted traumatic brain injury (ITBI) or shaken baby syndrome (SBS) in Estonia

M. Väli, I. Talvik, T. Metsvaht, 2006 .

T. Reimand, K. Õunap, P. Ilves, 2016, Neuropediatrics.

Targeted next generation sequencing as a diagnostic tool in 644 childhood epilepsy patients and transmission of variants from mosaic parents

P. Striano, R. Møller, A. Bayat, 2017 .

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

P. Ilves, I. Talvik, T. Talvik, 2010, Acta paediatrica.

Prevalence of Childhood Epilepsy in Estonia

I. Talvik, T. Talvik, I. Talvik, 1999, Epilepsia.

Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiency

T. Meitinger, T. Strom, R. Rodenburg, 2018, European Journal of Human Genetics.

Correction to: The landscape of epilepsy-related GATOR1 variants

Anne de Saint Martin, A. Biraben, F. Bartolomei, 2018, Genetics in Medicine.

The Incidence of Childhood Traumatic Brain Injury in Tartu and Tartu County in Estonia

M. Väli, I. Talvik, T. Talvik, 2008, Neuroepidemiology.

A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children

R. Rodenburg, K. Õunap, L. P. Van den Heuvel, 2012, Molecular Syndromology.

Incidence of childhood epilepsy in Estonia

I. Talvik, T. Talvik, A. Sööt, 1999, Brain and Development.

De novo variants in neurodevelopmental disorders with epilepsy

M. Daly, P. May, Sitao Wu, 2018, Nature Genetics.

author-version of: De novo variants in neurodevelopmental disorders with epilepsy

J. Serratosa, J. Kosmicki, Manuela Pendziwiat, 2022 .

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

I. Talvik, T. Talvik, M. Segawa, 2010, Brain and Development.

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

I. Talvik, T. Talvik, A. Piirsoo, 2003, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.