Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nuška Pečarič-Meglič"'
Autor:
Alja Kavčič, Zvonka Rener Primec, Mirjana Perković Benedik, Nuška Pečarič Meglič, Damjan Osredkar
Publikováno v:
Zdravniški Vestnik, Vol 88, Iss 3-4, Pp 184-196 (2019)
Ishemična možganska kap je v pediatrični populaciji redka, vendar predstavlja pomemben vzrok nevrološke oviranosti pri otrocih in mladostnikih. Z razvojem in dostopnostjo nevroradiološke diagnostike je danes prepoznava ishemične možganske kapi
Externí odkaz:
https://doaj.org/article/a260642a75c24e20b93f7fd7bc56b39d
Publikováno v:
Documenta Ophthalmologica. 146:121-136
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51e0578b0a5ba19f5b8e9be55426da23
https://doi.org/10.1007/s10633-023-09920-3
https://doi.org/10.1007/s10633-023-09920-3
Autor:
Tanja, Višnjar, Aleš, Maver, Karin, Writzl, Ornela, Maloku, Gaber, Bergant, Helena, Jaklič, David, Neubauer, Federico, Fogolari, Nuška, Pečarič Meglič, Borut, Peterlin
Publikováno v:
Neurology. Genetics. 8(3)
To report on the novel association of biallelic variant in atonal basic helix-loop-helix transcription factor 1 (A detailed clinical assessment and exome sequencing of peripheral blood sample were performed. Segregation analysis with Sanger sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49b8bdb65414d2f1ddb6c4f5ae654372
https://pubmed.ncbi.nlm.nih.gov/35518571
https://pubmed.ncbi.nlm.nih.gov/35518571
Publikováno v:
Zdravniški Vestnik, Vol 88, Iss 3-4, Pp 184-196 (2019)
Ishemična možganska kap je v pediatrični populaciji redka, vendar predstavlja pomemben vzrok nevrološke oviranosti pri otrocih in mladostnikih. Z razvojem in dostopnostjo nevroradiološke diagnostike je danes prepoznava ishemične možganske kapi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8651faadefa629de62ee989a327bc61
https://doi.org/10.6016/zdravvestn.2802
https://doi.org/10.6016/zdravvestn.2802
Autor:
Zvonka Rener Primec, Karin Writzl, Hirotomo Saitsu, Damjan Osredkar, Kiyomi Nishiyama, Naomichi Matsumoto, Branka Stirn Kranjc, Nuška Pečarič-Meglič, Barbara Gnidovec Stražišar
Publikováno v:
Epilepsia. 53:e106-e110
Recent study has shown that mutations in the alpha-II-spectrin (SPTAN1) gene cause early onset intractable seizures, severe developmental delay, diffuse hypomyelination, and widespread brain atrophy. We report a Slovene girl with hypotonia, lack of v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67cd4ff114de6fb880be7014e45a18e5
https://doi.org/10.1111/j.1528-1167.2012.03437.x
https://doi.org/10.1111/j.1528-1167.2012.03437.x
Publikováno v:
Documenta Ophthalmologica. 124:109-123
Achiasmia is a rare disorder of visual pathway maldevelopment that can show diverse clinical and magnetic resonance imaging spectra. The aim of this study was to define the characteristics of visual evoked potentials (VEPs) that differentiate abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bf1be7ccbb8651b8506042107af98a7
https://doi.org/10.1007/s10633-012-9315-4
https://doi.org/10.1007/s10633-012-9315-4
Autor:
Blaž Koritnik, Vlasta Zupanc Isoski, Aleš Belič, Nuška Pečarič Meglič, Janez Žibert, Grega Repovs, Veronika Rutar Gorišek, Janez Zidar, Matej Vrabec, Christina Manouilidou, Jure Bon
Publikováno v:
Brain and language. 163
Broca's region and adjacent cortex presumably take part in working memory (WM) processes. Electrophysiologically, these processes are reflected in synchronized oscillations. We present the first study exploring the effects of a stroke causing Broca's
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::304234d116d909a67fe67ff91e9e4664
https://pubmed.ncbi.nlm.nih.gov/27631161
https://pubmed.ncbi.nlm.nih.gov/27631161
Publikováno v:
European journal of pediatrics. 172(2)
Arterial ischemic stroke is an important cause of morbidity and mortality in pediatric population. A right-to-left shunt (RLS) across the patent foramen ovale was recently demonstrated as a possible risk factor for pediatric stroke. Prothrombotic dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8af1491d06f3cbab891e15dcfb80a6d3
https://pubmed.ncbi.nlm.nih.gov/23108849
https://pubmed.ncbi.nlm.nih.gov/23108849
Autor:
Karin, Writzl, Zvonka Rener, Primec, Barbara Gnidovec, Stražišar, Damjan, Osredkar, Nuška, Pečarič-Meglič, Branka Stirn, Kranjc, Kiyomi, Nishiyama, Naomichi, Matsumoto, Hirotomo, Saitsu
Publikováno v:
Epilepsia. 53(6)
Recent study has shown that mutations in the alpha-II-spectrin (SPTAN1) gene cause early onset intractable seizures, severe developmental delay, diffuse hypomyelination, and widespread brain atrophy. We report a Slovene girl with hypotonia, lack of v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::68dcd85167a9f37cf7216efb00a3efd6
https://pubmed.ncbi.nlm.nih.gov/22429196
https://pubmed.ncbi.nlm.nih.gov/22429196
Autor:
Milica Gregorič Kramberger, Vita Štukovnik, Anja Čuš, Grega Repovš, Petra Tomše, Nuška Pečarič Meglič, Zdenko Garašević, Jože Jensterle, Zvezdan Pirtošek
Publikováno v:
Psychiatria Danubina
Volume 22
Issue 3
Volume 22
Issue 3
Background: The main clinical feature of dementia in Parkinson's disease is a dysexecutive syndrome. The neuropathology of PD dementia (PDD) is likely multifactorial and affects several neuronal populations. There is evidence that Parkinson’s disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______951::2d34042401238575e202ce7cd7302e9c
https://hrcak.srce.hr/file/113443
https://hrcak.srce.hr/file/113443