Research Topics
| Ilona KopytaSummaryCountry: Poland Publications
| Collaborators |
Detail Information
Publications
[Chickenpox--neurological complications in children]Ilona Kopyta
Katedry i Kliniki Pediatrii i Neurologii Wieku Rozwojowego Slaskiego Uniwersytetu Medycznego w Katowicach
Wiad Lek 60:470-4. 2007..The neurological complications of chickenpox did not result in permanent sequel but the cost of hospitalization and the exclusion of the child from everyday activity seem to justify the idea of the routine vaccination...
[Schizencephaly--clinical and radiological presentation of pediatric patients]Ilona Kopyta
Z Katedry i Kliniki Pediatrii i Neurologii Wieku Rozwojowego Slaskiej Akademii Medycznej, Katowice
Wiad Lek 59:471-6. 2006..We did not found the correlation between the type of anomaly and clinical course, the degree of developmental delay and the severity of epilepsy in our group patients...
[Campylobacter jejuni infection in patient with Guillain-Barré syndrome: a case report]Ilona Kopyta
Katedra i Klinika Pediatrii i Neurologii Wieku Rozwojowego, Slaskiego Uniwersytetu Medycznego, Katowice
Med Dosw Mikrobiol 60:59-63. 2008..The identity of C. jejuni was also confirmed by a specific PCR. According to the authors' knowledge this is the first case of a patient with GBS with confirmed C. jejuni infection reported from Poland...
Association between lipids and fibrinogen levels and ischemic stroke in the population of the Polish children with arteriopathy and cardiac disordersIlona Kopyta
Katedra i Klinika Pediatrii i Neurologii Wieku Rozwojowego Slaskiego Uniwersytetu Medycznego w Katowicach
Wiad Lek 63:17-23. 2010..Cardiac problems, arteriopathy, coaguopathies or dyslipidemia are traditional risk factors for stroke. The aim of the present study was to assess the relations between levels of lipids and fibrinogen and stroke among Polish children...
Angelman syndrome revisitedJustyna Paprocka
Child Neurology Department, Medical University of Silesia, Katowice, Poland
Neurologist 13:305-12. 2007..It is caused by deficiency of gene expression from maternally derived chromosome 15q11-q13...
