Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Natalija Krajnc"'
Autor:
Andrej Vranič, Natalija Krajnc
Publikováno v:
Zdravniški Vestnik, Vol 87, Iss 5-6 (2018)
Epilepsy surgery is a branch of functional neurosurgery, developed for treating patients with resistant epilepsy in pediatric and adult population. The etiology and clinical picture of pediatric epilepsy are very heterogeneous and patients who could
Externí odkaz:
https://doaj.org/article/3b9a8ee4090b4a8b9ad3534cf732d3ae
Publikováno v:
Acta Clinica Croatica
Acta clinica Croatica
Volume 58.
Issue 2.
Acta clinica Croatica
Volume 58.
Issue 2.
To review the outcome of vagus nerve stimulation (VNS) therapy in all implanted Slovenian patients with drug-resistant epilepsy, data on 48 patients implanted between 2001 and 2015 were obtained retrospectively from medical records. The outcome was a
Autor:
Luka Kopač, Tadej Avcin, Blaž Kosmač, Samo Vesel, Rina Rus, Natalija Krajnc, Nataša Toplak, Matjaž Homan, Urška Kočevar
Publikováno v:
European Journal of Pediatrics. 176:23-29
A decline in the incidence of acute rheumatic fever (ARF) in developed countries over the past century can be attributed to the improved public hygiene and to widespread use of antibiotics. ARF seemed to be a rare disease in southern central European
Autor:
Andrej Vranič, Natalija Krajnc
Publikováno v:
Slovenian Medical Journal. 87
Epilepsy surgery is a branch of functional neurosurgery, developed for treating patients with resistant epilepsy in pediatric and adult population. The etiology and clinical picture of pediatric epilepsy are very heterogeneous and patients who could
Autor:
Natalija Krajnc
Publikováno v:
Journal of Child Neurology. 29:NP118-NP121
Rett syndrome is a neurodevelopmental disorder that manifests itself early in childhood, progresses with the evolution of characteristic clinical signs and symptoms and is confirmed by mutation in the methyl-CpG-binding protein 2 gene. Seizures are p
Autor:
Natalija Krajnc, Janez Zidar
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 20(4)
Rett syndrome (RTT) is a frequent neurodevelopmental disorder confirmed by clinical criteria and supported by the methyl-CpG-binding protein 2 gene (MECP2) mutation. A short central motor conduction time (CMCT) was reported in transcranial magnetic s
Publikováno v:
Paediatria Croatica
Volume 58
Issue 4
Volume 58
Issue 4
Autor:
Natalija Krajnc
Publikováno v:
Therapeutics and Clinical Risk Management
Rett syndrome (RTT) is a common neurodevelopmental disorder that appears in infancy with regression of acquired motor skills, loss of purposeful activity, hand stereotypies, loss of acquired spoken language, and seizures. Epilepsy affects the majorit
Autor:
Toplak, Nataša, Homan, Matjaž, Avčin, Tadej, Kočevar, Urška1, Kosmač, Blaž2, Vesel, Samo2, Kopač, Luka3, Krajnc, Natalija3, Rus, Rina4, Kočevar, Urška5 (AUTHOR), Toplak, Nataša5,6 (AUTHOR), Kosmač, Blaž7 (AUTHOR), Kopač, Luka8 (AUTHOR), Homan, Matjaž6,9 (AUTHOR), Avčin, Tadej5,6 (AUTHOR)
Publikováno v:
European Journal of Pediatrics. Jan2017, Vol. 176 Issue 1, p23-29. 7p.
Autor:
Krajnc, Natalija1 natalija.krajnc@mf.uni-lj.si
Publikováno v:
Therapeutics & Clinical Risk Management. Jun2015, Vol. 11, p925-932. 8p.