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Sleep and prematurity: sleep outcomes in preterm children and influencing factors

World journal of pediatrics : WJP, 2019-06, Vol.15 (3), p.209-218

2019

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Facial nerve palsy in childhood

Brain & development (Tokyo. 1979), 2011-09, Vol.33 (8), p.644-650

2011

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Posterior cerebral artery dissection after excessive caffeine consumption in a teenager

Radiology case reports, 2022-06, Vol.17 (6), p.2081-2084

2022

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Ketosis and EEG improvement following viral gastroenteritis in patient with West syndrome

Brain & development (Tokyo. 1979), 2014-05, Vol.36 (5), p.411-412

2014

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A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus–Merzbacher disease: A new MRI finding

Brain & development (Tokyo. 1979), 2017-03, Vol.39 (3), p.271-274

2017

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Facial nerve palsy in childhood

Brain & development (Tokyo. 1979), 2012-05, Vol.34 (5), p.405-405

2012

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Efficacy of antiepileptic drugs in the era of pharmacogenomics: A focus on childhood

European journal of paediatric neurology, 2019-09, Vol.23 (5), p.674-684

2019

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Therapies that are available and under development for Duchenne muscular dystrophy: What about lung function?

Pediatric pulmonology, 2020-02, Vol.55 (2), p.300-315

2020

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Emerging genetic influences in benign epilepsy with centro-temporal spikes – BECTS

Epilepsy research, 2012-09, Vol.101 (3), p.197-201

2012

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Branched Chain Amino Acids as Adjunctive Therapy to Ketogenic Diet in Epilepsy: Pilot Study and Hypothesis

Journal of child neurology, 2009-10, Vol.24 (10), p.1268-1272

2009

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Infantile Spasms (West Syndrome) in Children With Inborn Errors of Metabolism: A Review of the Literature

Journal of child neurology, 2012-10, Vol.27 (10), p.1295-1301

2012

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Learning disorders in children with epilepsy

Child's nervous system, 2011-03, Vol.27 (3), p.373-379

2011

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Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1 :c. 501C > G variant as a genetic modifier

Muscle & nerve, 2024-08, Vol.70 (2), p.240-247

2024

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Is the prevalence of thyroid disease higher in children receiving antiepileptic medication? A systematic review and meta-analysis

Seizure (London, England), 2022-01, Vol.94, p.117-125

2022

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Sleep Disturbances in Children with Rolandic Epilepsy

Neuropediatrics, 2017-02, Vol.48 (1), p.30-35

2017

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Vaccination and neurological disorders

Journal of pediatric sciences, 2015-04, Vol.7

2015

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Septic pulmonary embolism due to Staphylococcus aureus

Pediatrics international, 2008-10, Vol.50 (5), p.717-717

2008

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

Orphanet journal of rare diseases, 2018-09, Vol.13 (1), p.157-157, Article 157

2018

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Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier

Muscle & nerve, 2024-08, Vol.70 (2), p.240-247

2024

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Assessment of Sleep Quality in Adolescents with Overweight and Obesity Using the Adolescent Sleep Hygiene Scale (ASHS)

Children (Basel), 2024-11, Vol.11 (11), p.1372

2024

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Circulating serum and plasma levels of micro‐RNA in type‐1 diabetes in children and adolescents: A systematic review and meta‐analysis

European journal of clinical investigation, 2021-07, Vol.51 (7), p.e13510-n/a

2021

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Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study

Epilepsia open, 2019-03, Vol.4 (1), p.73-84

2019

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

Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.301-301, Article 301

2021

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Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population

Epilepsy research, 2014-12, Vol.108 (10), p.1734-1739

2014

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Sleep and prematurity: sleep outcomes in preterm children and influencing factors

Facial nerve palsy in childhood

Posterior cerebral artery dissection after excessive caffeine consumption in a teenager

Ketosis and EEG improvement following viral gastroenteritis in patient with West syndrome

A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus–Merzbacher disease: A new MRI finding

Facial nerve palsy in childhood

Efficacy of antiepileptic drugs in the era of pharmacogenomics: A focus on childhood

Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years

Therapies that are available and under development for Duchenne muscular dystrophy: What about lung function?

Emerging genetic influences in benign epilepsy with centro-temporal spikes – BECTS

Branched Chain Amino Acids as Adjunctive Therapy to Ketogenic Diet in Epilepsy: Pilot Study and Hypothesis

Infantile Spasms (West Syndrome) in Children With Inborn Errors of Metabolism: A Review of the Literature

Learning disorders in children with epilepsy

Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1 :c. 501C > G variant as a genetic modifier

Is the prevalence of thyroid disease higher in children receiving antiepileptic medication? A systematic review and meta-analysis

Sleep Disturbances in Children with Rolandic Epilepsy

Vaccination and neurological disorders

Septic pulmonary embolism due to Staphylococcus aureus

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

Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier

Assessment of Sleep Quality in Adolescents with Overweight and Obesity Using the Adolescent Sleep Hygiene Scale (ASHS)

Circulating serum and plasma levels of micro‐RNA in type‐1 diabetes in children and adolescents: A systematic review and meta‐analysis

Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study

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

Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population

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