Search Results - "Stawicka, Elżbieta"

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  1. 1

    Enhancing autism spectrum disorder classification in children through the integration of traditional statistics and classical machine learning techniques in EEG analysis by Rogala, Jacek, Żygierewicz, Jarosław, Malinowska, Urszula, Cygan, Hanna, Stawicka, Elżbieta, Kobus, Adam, Vanrumste, Bart

    Published in Scientific reports (08-12-2023)
    “…Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder hallmarked by challenges in social communication, limited interests, and repetitive,…”
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    Journal Article
  2. 2

    Epilepsy, EEG and chromosomal rearrangements by Paprocka, Justyna, Coppola, Antonietta, Cuccurullo, Claudia, Stawicka, Elżbieta, Striano, Pasquale

    Published in Epilepsia open (01-08-2024)
    “…Chromosomal abnormalities are associated with a broad spectrum of clinical manifestations, one of the more commonly observed of which is epilepsy. The…”
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  3. 3

    A current view of mitochondria damage and the diversity of lipopigment inclusions in neuronal ceroid lipofuscinose type 2 from rectal biopsy by Felczak, Paulina, Kuźniar-Pałka, Aleksandra, Ługowska, Agnieszka, Stawicka, Elżbieta, Tarka, Sylwia, Mierzewska, Hanna

    Published in Folia neuropathologica (01-01-2024)
    “…Neuronal ceroid lipofuscinoses (NCLs) are a growing group of neurodegenerative storage diseases, in which specific features are sought to facilitate the…”
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    Journal Article
  4. 4

    Anti-NMDA receptor encephalitis – the narrative review of literature with particular regard to pediatric population by Stawicka, Elżbieta

    Published in Psychiatria polska (31-12-2022)
    “…W ostatnich latach znacząco zwiększyła się częstość rozpoznawania zapaleń mózgu o etiologii autoimmunologicznej, zarówno w populacji pacjentów dorosłych, jak i…”
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  5. 5

    SCN1A -Characterization of the Gene's Variants in the Polish Cohort of Patients with Dravet Syndrome: One Center Experience by Stawicka, Elżbieta, Zielińska, Anita, Górka-Skoczylas, Paulina, Kanabus, Karolina, Tataj, Renata, Mazurczak, Tomasz, Hoffman-Zacharska, Dorota

    Published in Current issues in molecular biology (07-05-2024)
    “…The aim of this study was to characterize the genotype and phenotype heterogeneity of patients with gene mutations in the Polish population, fulfilling the…”
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  6. 6
  7. 7

    Mania induced by antidepressants - characteristics and specific phenomena in children and adolescents by Stawicka, Elżbieta, Wolańczyk, Tomasz

    Published in Psychiatria polska (30-06-2020)
    “…The phenomenon of drug-induced mania, i.e., a manic episode associated with the use of pharmacotherapy (in particular antidepressants) is well defined and…”
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  8. 8

    How Has the Treatment of Polish Children with Dravet Syndrome Changed? Future Perspectives by Zielińska, Anita, Skarżyńska, Urszula, Górka-Skoczylas, Paulina, Mazurczak, Tomasz, Kuźniar-Pałka, Aleksandra, Kanabus, Karolina, Hoffman-Zacharska, Dorota, Stawicka, Elżbieta

    Published in Biomedicines (01-06-2024)
    “…This report focuses on the treatment histories of 21 patients diagnosed with Dravet syndrome (DRVT) under the care of the Mother and Child Institute in Warsaw…”
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    Journal Article
  9. 9

    A new look at the clinical and molecular characteristics of SCN1A-related developmental and epileptic encephalopathies by Stawicka, Elżbieta, Górka-Skoczylas, Paulina, Hoffman-Zacharska, Dorota

    Published in Aktualności neurologiczne (07-12-2022)
    “…SCN1A-related diseases are a heterogeneous group of disorders with an expanding spectrum of phenotypes. Until recently, mutations in this gene were associated…”
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    Journal Article
  10. 10

    Anti-NMDA receptor encephalitis - the narrative review of literature with particular regard to pediatric population by Stawicka, Elżbieta

    Published in Psychiatria polska (31-12-2022)
    “…In recent years, the frequency of diagnosing autoimmune encephalitis has increased significantly, both in the population of adults and children and…”
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    Journal Article
  11. 11

    A current view of mitochondria damage and the diversity of lipopigment inclusions in neuronal ceroid lipofuscinose type 2 from rectal biopsy by Felczak, Paulina, Kuźniar-Pałka, Aleksandra, Ługowska, Agnieszka, Stawicka, Elżbieta, Tarka, Sylwia, Mierzewska, Hanna

    Published in Folia neuropathologica (2024)
    “…Neuronal ceroid lipofuscinoses (NCLs) are a growing group of neurodegenerative storage diseases, in which specific features are sought to facilitate the…”
    Get more information
    Journal Article