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Wyświetlanie 1-2 z 2
Tytuł:
Epilepsy in paediatric patients with schizencephaly
Autorzy:
Kopyta, I.
Skrzypek, M.
Raczkiewicz, D.
Bojar, I.
Sarecka-Hujar, B.
Powiązania:
https://bibliotekanauki.pl/articles/2085589.pdf
Data publikacji:
2020
Wydawca:
Instytut Medycyny Wsi
Tematy:
schizencephaly
bilateral
unilateral
central nervous system malformation
epilepsy
developmental delay
Opis:
Introduction. Schizencephaly is one of the rare congenital defects of the central nervous system (CNS), known as neuronal migration disorders. The etiology of schizencecephaly is unequivocal. Established etiologies include in-utero infections (cytomegalovirus and herpes simplex virus, HSV type I), toxic abuse (cocaine, alcohol), as well as drug use (warfarin). Objectives. The aim of the study was to analyze the clinical presentation of schizencephaly with particular consideration of the course of epilepsy in paediatric patients. Materials and method. The study group consisted of 38 children with schizencephaly (20 of them had seizure) and was retrospectively assessed. Data were analyzed using SAS version 9.4. U Mann-Whitney and χ2 tests and logistic regression analysis were used in statistical analyses. Results. Epilepsy was the most frequent in bilateral type II schizencephaly (p=0.033). In logistic regression analysis, the presence of bilateral open schizencephaly significantly increased the risk of seizures (OR=11.67; 95%CI 2.44–55.83; p=0.002). Drug-resistant epilepsy was observed in 9 children (45% of the children with epilepsy). Prevalence of both epilepsy and drug-resistant epilepsy in schizencephaly did not significantly depend on gender, stage of development, type or localization of schizencephaly, and other coexisting CNS defects or clinical presentation of schizencephaly at follow-up in the study group of patients. Conclusions. The bilateral type of schizencephaly was identified as an independent risk factor for epilepsy in the analyzed children.
Źródło:
Annals of Agricultural and Environmental Medicine; 2020, 27, 2; 279-283
1232-1966
Pojawia się w:
Annals of Agricultural and Environmental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Motor functions assessment method based on energy changes in gait cycle
Autorzy:
Michnik, R.
Nowakowska, K.
Jurkojč, J.
Jochymczyk-Woźniak, K.
Kopyta, I.
Powiązania:
https://bibliotekanauki.pl/articles/307383.pdf
Data publikacji:
2017
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
porażenie mózgowe
wydatek energetyczny
indeks chodu
cerebral palsy
energy expenditure
gait indice
Opis:
The aim of the research was to determine the energy changes during the gait cycle for a group of healthy children and a group of patients with cerebral palsy, and to compare the value of energy expenditure (EE) with the determined values of the Gillette Gait Index (GGI) and the Gait Deviation Index (GDI). Methods: The study group consisted of 56 children with regular gait and 56 patients with diagnosed cerebral palsy (CP). The gait kinematics was determined by BTS Smart System. Based on the identified position of the body mass, the following parameters were determined: the potential energy, kinetic energy, and total energy. The values were standardized to 100% of the gait cycle. The values of the Gillette Gait Index (GGI) and the Gait Deviation Index (GDI) were calculated using the authors’ own software. Results: Values of potential, kinematic and mechanical energy changes and mean values of total energy (energy expenditure – EE) were calculated for a reference group and for patients with CP. The obtained results were standardized in relation to the body mass and stride length. Furthermore, the values of the Gillette Gait Index (GGI) and the Gait Deviation Index (GDI) were calculated. Statistical analysis of the obtained results was performed. The Spearman rank correlation coefficient was defined between the calculated GGI and GDI values and energy expenditure EE. Conclusions: Values of energy expenditure changes can be used as an objective comparative tool for gait results concerning children with various neurological and orthopaedic dysfunctions.
Źródło:
Acta of Bioengineering and Biomechanics; 2017, 19, 4; 63-75
1509-409X
2450-6303
Pojawia się w:
Acta of Bioengineering and Biomechanics
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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