Publications by authors named "Jan Magielski"

Speech and language disorders are known to have a substantial genetic contribution. Although frequently examined as components of other conditions, research on the genetic basis of linguistic differences as separate phenotypic subgroups has been limited so far. Here, we performed an in-depth characterization of speech and language disorders in 52 143 individuals, reconstructing clinical histories using a large-scale data-mining approach of the electronic medical records from an entire large paediatric healthcare network.

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Introduction: Since the initial description of related hemiplegic migraine (HM), the phenotypic spectrum has expanded from mild episodes in neurotypical individuals to potentially life-threatening events frequently seen in individuals with developmental and epileptic encephalopathies. However, the overall longitudinal course throughout childhood remains unknown.

Methods: We analyzed HM and seizure history in individuals with -related HM, delineating frequency and severity of events in monthly increments through a standardized approach.

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The insights gained from big data and omics approaches have transformed the field of childhood genetic epilepsy. With an increasing number of individuals receiving genetic testing for seizures, we are provided with an opportunity to identify clinically relevant subgroups and extract meaningful observations from this large-scale clinical data. However, the volume of data from electronic medical records and omics (e.

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Speech and language disorders are known to have a substantial genetic contribution. Although frequently examined as components of other conditions, research on the genetic basis of linguistic differences as separate phenotypic subgroups has been limited so far. Here, we performed an in-depth characterization of speech and language disorders in 52,143 individuals, reconstructing clinical histories using a large-scale data mining approach of the Electronic Medical Records (EMR) from an entire large paediatric healthcare network.

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Article Synopsis
  • Individuals with STXBP1-related epilepsy often have seizures in their first year, including epileptic spasms, but the effects of early seizures and antiseizure medications (ASMs) on later seizure types are not well understood.
  • A study analyzed seizure and medication histories of 61 patients with early onset seizures, finding no increased risk of developing epileptic spasms from neonatal or early infantile seizures, nor any specific ASM linked to this development.
  • The research highlights that individuals with prior seizures are at risk for refractory epileptic spasms, but those with refractoriness experience a later onset of spasms, providing key insights for targeted treatment strategies.
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Background And Objectives: Individuals with disease-causing variants in frequently have epilepsy onset in the first year of life with a variety of seizure types, including epileptic spasms. However, the impact of early-onset seizures and anti-seizure medication (ASM) on the risk of developing epileptic spasms and impact on their trajectory is poorly understood, limiting informed and anticipatory treatment, as well as trial design.

Methods: We retrospectively reconstructed seizure and medication histories in weekly intervals for individuals with -related disorders with epilepsy onset in the first year of life and quantitatively analyzed longitudinal seizure histories and medication response.

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It is well-established that sleep and behavior are interrelated. Although studies have investigated this association, not many have evaluated the bidirectional relationship between the two. To our knowledge this is the first systematic review providing a comprehensive analysis of a reciprocal relationship between sleep and externalizing behavior.

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