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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

Epilepsia (Copenhagen), 2015-12, Vol.56 (12), p.e203-e208

2015

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P460: Electroencephalography and clinical findings in a SCN8A epileptic encephalopathy: a case report

Clinical neurophysiology, 2014-06, Vol.125, p.S171-S171

2014

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Factor V Leiden and prothrombin 21210G>A mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses

Acta Paediatrica, 2010-08, Vol.99 (8), p.1168-1174

2010

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Clean intermittent self-catheterization in persons with multiple sclerosis: the influence of cognitive dysfunction

Multiple sclerosis, 2009-03, Vol.15 (3), p.379-384

2009

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Prevalence of Childhood Epilepsy in Estonia

Epilepsia (Copenhagen), 1999-07, Vol.40 (7), p.1011-1019

1999

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Incidence of juvenile idiopathic arthritis in children in Estonia: a prospective population-based study

Scandinavian journal of rheumatology, 2007, Vol.36 (1), p.7-13

2007

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P202 – 2912: Methylenetetrahydrofolate reductase (MTHFR) polymorphisms A1298C and C677T as genetic risk factors for perinatal and childhood arterial ischemic stroke?

European journal of paediatric neurology, 2015-05, Vol.19, p.S150-S151

2015

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Cerebral blood-flow velocities in predicting outcome of asphyxiated newborn infants

Acta Paediatrica, 2004-04, Vol.93 (4), p.523-528

2004

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Cognitive dysfunction during anti-NMDA-receptor encephalitis is present in early phase of the disease

Oxford Medical Case Reports, 2014-07, Vol.2014 (4), p.74-76

2014

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One question as a screening instrument for depression in people with multiple sclerosis

Clinical rehabilitation, 2007-05, Vol.21 (5), p.460-464

2007

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Prevalence and short-term outcome of juvenile idiopathic arthritis: a population-based study in Estonia

Clinical and experimental rheumatology, 2007-07, Vol.25 (4), p.649

2007

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Cognitive Outcome of Children With Early-Onset Hemiparesis

Journal of child neurology, 2000-09, Vol.15 (9), p.581-587

2000

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Early clinical symptoms of perinatal stroke

European journal of paediatric neurology, 2008, Vol.12, p.S67-S67

2008

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P036 Magnetic resonance imaging in hypoxic-ischaemic encephalopathy

European journal of paediatric neurology, 2009, Vol.13, p.S32-S32

2009

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The reference limits and cut-off value for serum soluble transferrin receptors for diagnosing iron deficiency in infants

International journal of laboratory hematology, 2009-08, Vol.31 (4), p.440-446

2009

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CPO03 Magnetic resonance imaging (MRI) in diplegic cerebral palsy

European journal of paediatric neurology, 2007, Vol.11, p.34-35

2007

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Serum total magnesium and ionized calcium concentrations in asphyxiated term newborn infants with hypoxic-ischaemic encephalopathy

Acta Paediatrica, 2000-06, Vol.89 (6), p.680-685

2000

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The high frequency of coeliac disease among children with neurological disorders

European journal of neurology, 2000-12, Vol.7 (6), p.707-711

2000

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High mobility group box protein 1—A prognostic marker for structural joint damage in 10-year follow-up of patients with juvenile idiopathic arthritis

Seminars in arthritis and rheumatism, 2017-02, Vol.46 (4), p.444-450

2017

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Low Serum IGF-1 in Boys with Recent Onset of Juvenile Idiopathic Arthritis

Journal of Immunology Research, 2018-01, Vol.2018, p.3856897-10

2018

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Is the International League Against Epilepsy classification of epileptic syndromes applicable to children in Estonia?

European journal of paediatric neurology, 1999, Vol.3 (6), p.265-272

1999

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Sudden death of a girl with Prader-Willi syndrome

Genetic counseling, 2002, Vol.13 (4), p.459

2002

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Resuscitation of newborn infants with 21% or 100% oxygen: follow-up at 18 to 24 months

Pediatrics (Evanston), 2003-08, Vol.112 (2), p.296

2003

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Chronic Paroxysmal Hemicrania in a 3-Year, 10-Month-Old Female

Pediatric neurology, 2006-03, Vol.34 (3), p.225-227

2006

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

Neuroepidemiology, 2008-01, Vol.30 (1), p.20-24

2008

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

P460: Electroencephalography and clinical findings in a SCN8A epileptic encephalopathy: a case report

Factor V Leiden and prothrombin 21210G>A mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses

Clean intermittent self-catheterization in persons with multiple sclerosis: the influence of cognitive dysfunction

Prevalence of Childhood Epilepsy in Estonia

Incidence of juvenile idiopathic arthritis in children in Estonia: a prospective population-based study

P202 – 2912: Methylenetetrahydrofolate reductase (MTHFR) polymorphisms A1298C and C677T as genetic risk factors for perinatal and childhood arterial ischemic stroke?

Cerebral blood-flow velocities in predicting outcome of asphyxiated newborn infants

Cognitive dysfunction during anti-NMDA-receptor encephalitis is present in early phase of the disease

One question as a screening instrument for depression in people with multiple sclerosis

Prevalence and short-term outcome of juvenile idiopathic arthritis: a population-based study in Estonia

Cognitive Outcome of Children With Early-Onset Hemiparesis

Early clinical symptoms of perinatal stroke

P036 Magnetic resonance imaging in hypoxic-ischaemic encephalopathy

The reference limits and cut-off value for serum soluble transferrin receptors for diagnosing iron deficiency in infants

CPO03 Magnetic resonance imaging (MRI) in diplegic cerebral palsy

Serum total magnesium and ionized calcium concentrations in asphyxiated term newborn infants with hypoxic-ischaemic encephalopathy

The high frequency of coeliac disease among children with neurological disorders

High mobility group box protein 1—A prognostic marker for structural joint damage in 10-year follow-up of patients with juvenile idiopathic arthritis

Low Serum IGF-1 in Boys with Recent Onset of Juvenile Idiopathic Arthritis

Is the International League Against Epilepsy classification of epileptic syndromes applicable to children in Estonia?

Sudden death of a girl with Prader-Willi syndrome

Resuscitation of newborn infants with 21% or 100% oxygen: follow-up at 18 to 24 months

Chronic Paroxysmal Hemicrania in a 3-Year, 10-Month-Old Female

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

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