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Genetic Risk Factors for Neurological Disorders in Children with Adverse Events Following Immunization: A Descriptive Study of a Polish Case Series

International journal of molecular sciences, 2023-01, Vol.24 (2), p.1117

2023

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Magnetic resonance imaging of neonates in the magnetic resonance compatible incubator

Archives of medical science, 2016-10, Vol.12 (5), p.1064-1070

2016

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Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females

Genetics in medicine, 2011-05, Vol.13 (5), p.447-452

2011

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Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2012-10, Vol.159B (7), p.760-771

2012

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Intrathecal Infusion of Autologous Adipose-Derived Regenerative Cells in Autoimmune Refractory Epilepsy: Evaluation of Safety and Efficacy

Stem cells international, 2020, Vol.2020 (2020), p.1-16

2020

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Use of Fibrin Glue in the Treatment of Persistent Pneumothorax in Premature Infants at the Limit of Viability: Ethical Issues and Two and A Half Years Follow-Up

Journal of Mother and Child, 2023-06, Vol.27 (1), p.190-197

2023

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PIGN encephalopathy: Characterizing the epileptology

Epilepsia (Copenhagen), 2022-04, Vol.63 (4), p.974-991

2022

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Hypertrophic olivary degeneration in a 16-year-old girl after subtotal surgery of a brainstem pilocytic astrocytoma - a case report

Polish journal of radiology, 2019, Vol.84, p.e68-72

2019

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Patterns of the EEG records in children with West Syndrome

Przeglad lekarski, 2015, Vol.72 (11), p.694

2015

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Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance

Journal of applied genetics, 2015-02, Vol.56 (1), p.49-56

2015

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Decoding working memory-related information from repeated psychophysiological EEG experiments using convolutional and contrastive neural networks

Journal of neural engineering, 2022-08, Vol.19 (4), p.46053

2022

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Neurosurgical treatment of drug-resistant epilepsy on the basis of a fusion of MRI and SPECT images - case report

Polish journal of radiology, 2010-01, Vol.75 (3), p.51-54

2010

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Neonatal Seizures do not Exclude Dravet Syndrome Diagnosis

Journal of neurology & neurophysiology, 2016, Vol.7 (2)

2016

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Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2

Przeglad lekarski, 2010, Vol.67 (9), p.757

2010

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Comprehensive genomic analysis of patients with disorders of cerebral cortical development

European journal of human genetics : EJHG, 2018-08, Vol.26 (8), p.1121-1131

2018

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From focal epilepsy to Dravet syndrome – Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit

Neurologia i neurochirurgia polska, 2015-01, Vol.49 (4), p.258-266

2015

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Clinical heterogeneity of West syndrome - the possibilities and limitations of molecular diagnostics

Folia neuropathologica, 2014-01, Vol.52 (4), p.469-469

2014

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Glucose transporter type 1 deficiency due to SLC2A1 gene mutations--a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review

Medycyna wieku rozwojowego, 2015-10, Vol.19 (4), p.454

2015

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An early infantile epileptic encephalopathy 19 with dyskinesias due to a new GABRA1 gene mutation – identification of the first case in the Polish population

Child Neurology, 2017, Vol.26 (53), p.67-70

2017

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Genetic epilepsies with febrile seizures plus: clinical spectrum of Polish patients with SCN1A mutation - preliminary report

Medycyna wieku rozwojowego, 2014-10, Vol.18 (4), p.426

2014

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The perturbations in the neuronal interaction - a possible cause of the epileptic encephalopathy related to mutations in the PCDH19 gene

Folia neuropathologica, 2014-01, Vol.52 (4), p.472-472

2014

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Mutations in the SCN1A gene and what else... analysis of the molecular background of epileptic encephalopathy in Polish patients clinically diagnosed with Dravet syndrome

Folia neuropathologica, 2014-01, Vol.52 (4), p.470-470

2014

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Hypertrophic olivary degeneration in a 16-year-old girl after subtotal surgery of a brainstem pilocytic astrocytoma - a case report

Polish journal of radiology, 2019, Vol.84, p.e68-e72

2019

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Neurosurgical treatment of drug-resistant epilepsy on the basis of a fusion of MRI and SPECT images - case report

Polish journal of radiology, 2010, Vol.75 (3), p.51-54

2010

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Genetic Risk Factors for Neurological Disorders in Children with Adverse Events Following Immunization: A Descriptive Study of a Polish Case Series

Magnetic resonance imaging of neonates in the magnetic resonance compatible incubator

Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females

Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders

Intrathecal Infusion of Autologous Adipose-Derived Regenerative Cells in Autoimmune Refractory Epilepsy: Evaluation of Safety and Efficacy

Use of Fibrin Glue in the Treatment of Persistent Pneumothorax in Premature Infants at the Limit of Viability: Ethical Issues and Two and A Half Years Follow-Up

PIGN encephalopathy: Characterizing the epileptology

Hypertrophic olivary degeneration in a 16-year-old girl after subtotal surgery of a brainstem pilocytic astrocytoma - a case report

Patterns of the EEG records in children with West Syndrome

Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance

Decoding working memory-related information from repeated psychophysiological EEG experiments using convolutional and contrastive neural networks

Neurosurgical treatment of drug-resistant epilepsy on the basis of a fusion of MRI and SPECT images - case report

Neonatal Seizures do not Exclude Dravet Syndrome Diagnosis

Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2

Comprehensive genomic analysis of patients with disorders of cerebral cortical development

From focal epilepsy to Dravet syndrome – Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit

Clinical heterogeneity of West syndrome - the possibilities and limitations of molecular diagnostics

Glucose transporter type 1 deficiency due to SLC2A1 gene mutations--a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review

An early infantile epileptic encephalopathy 19 with dyskinesias due to a new GABRA1 gene mutation – identification of the first case in the Polish population

Genetic epilepsies with febrile seizures plus: clinical spectrum of Polish patients with SCN1A mutation - preliminary report

The perturbations in the neuronal interaction - a possible cause of the epileptic encephalopathy related to mutations in the PCDH19 gene

Mutations in the SCN1A gene and what else... analysis of the molecular background of epileptic encephalopathy in Polish patients clinically diagnosed with Dravet syndrome

Hypertrophic olivary degeneration in a 16-year-old girl after subtotal surgery of a brainstem pilocytic astrocytoma - a case report

Neurosurgical treatment of drug-resistant epilepsy on the basis of a fusion of MRI and SPECT images - case report

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