Terkko Navigator / Lönnqvist, T(uula) (PRC)*

Left-handedness should not be overrated as a risk factor for postoperative speech impairment in children after posterior fossa tumour surgery: a prospective European multicentre study

Hearing outcome in congenitally CMV infected children in Finland - Results from follow-up after three years age

Health-related quality of life in long-term survivors of childhood brain tumors: a population-based cohort study

Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype

Cost-effectiveness of whole-exome sequencing in progressive neurological disorders of children

Postoperative speech impairment and surgical approach to posterior fossa tumours in children: a prospective European multicentre cohort study

Infantile-Onset Spinocerebellar Ataxia

Neurocognitive impairment, employment, and social status in radiotherapy-treated adult survivors of childhood brain tumors

Diagnostic value of serum biomarkers FGF21 and GDF15 compared to muscle sample in mitochondrial disease

Screening of hydrocephalus in infants using either WHO or population-based head circumference reference charts

Radiation-induced accelerated aging of the brain vasculature in young adult survivors of childhood brain tumors

Genetic background of ataxia in children younger than 5 years in Finland

Attitudes towards genetic testing and information: does parenthood shape the views?

Viral shedding, and distribution of cytomegalovirus glycoprotein H (UL75), glycoprotein B (UL55), and glycoprotein N (UL73) genotypes in congenital cytomegalovirus infection

Topological Alterations of the Structural Brain Connectivity Network in Children with Juvenile Neuronal Ceroid Lipofuscinosis

The spectrum of acute central nervous system symptoms during the treatment of childhood acute lymphoblastic leukaemia

Radiation-Induced Meningiomas After Childhood Brain Tumor: A Magnetic Resonance Imaging Screening Study

Bedside neurophysiological tests can identify neonates with stroke leading to cerebral palsy

Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers

Evaluation of SEPs in asphyxiated newborns using a 4-electrode aEEG brain monitoring set-up

Global and Widespread Local White Matter Abnormalities in Juvenile Neuronal Ceroid Lipofuscinosis

The Burden of Congenital Cytomegalovirus Infection: A Prospective Cohort Study of 20 000 Infants in Finland

Reply to 'Letter to Editor by Finsterer J and Zarrouk-Mahjoub S: Phenotypic manifestations of the m.8969G>A variant'

Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth

Posterior Reversible Encephalopathy Syndrome: Risk Factors and Impact on the Outcome in Children With Acute Lymphoblastic Leukemia Treated With Nordic Protocols

Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients

Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

A recessive ataxia diagnosis algorithm for the next generation sequencing era

Cerebellar mutism syndrome in children with brain tumours of the posterior fossa

MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability

Evoked potentials recorded during routine EEG predict outcome after perinatal asphyxia

ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss

Neonatal somatosensory evoked potentials persist during hypothermia

Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

Primary versus non-primary maternal cytomegalovirus infection as a cause of symptomatic congenital infection - register-based study from Finland

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy

Dysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsy

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

Metronomic therapy can increase quality of life during paediatric palliative cancer care, but careful patient selection is essential

Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate

Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia

Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy

Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion

A multicenter study on Leigh syndrome: disease course and predictors of survival

Neurocognitive long term follow-up study on drowned children

Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine glioma

How do I tell about a severe illness of a child?

Motor development of infants with univentricular heart at the ages of 16 and 52 weeks