Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Daniela Deneva"'
Publikováno v:
Българска неврология, Vol 24, Iss 3 (2023)
Тубулинът е протеин, който полимеризира в дълги вериги или нишки, които образуват микротрубули, имащи ключова роля в клетъчното делене,
Externí odkaz:
https://doaj.org/article/3e892f1dd3964ba89d9330d885d31a2f
Publikováno v:
Българска неврология, Vol 22, Iss 1 (2021)
Синдромът на Knobloch е рядко и клинично хетерогенно автозомно-рецесивно заболяване, дължащо се на мутации в COL18A1. Генът е разположен в дълго
Externí odkaz:
https://doaj.org/article/7360ab15442e4431af4f0e1b6c884df1
Autor:
Iliyana Aleksandrova, Asya Asenova, Petia Dimova, Daniela Deneva, Elena Rodopska, Elena Slavkova, Veneta Bojinova
Publikováno v:
Journal of Child Science. 13:e40-e46
Background The efforts of clinicians are focused on determining the predictors for electrical status epilepticus in sleep (ESES) manifestation, due to the negative effect of ESES on cognition. Treatment approaches remain a leading problem because of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a2559c74663dba97090d6cf9625d891
https://doi.org/10.1055/s-0043-1768463
https://doi.org/10.1055/s-0043-1768463
Autor:
Elena Rodopska, Nikolay Topalov, Iliana Aleksandrova, Asya Asenova, Daniela Deneva, Maya Koleva, Elena Slavkova, Veneta Bojinova
Publikováno v:
Proceedings of the Bulgarian Academy of Sciences. 75:1852-1858
Epilepsy is common in children with cerebral palsy (CP). In a group of 521 children with cerebral palsy it was found that 58% (n = 303) of the affected had epilepsy and 74.5% (n = 388) had mental retardation. We found ahigher percentage of symptomati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::346200e71c386f30901896d9a8ba282f
https://doi.org/10.7546/crabs.2022.12.18
https://doi.org/10.7546/crabs.2022.12.18
Publikováno v:
Journal of Child Science. 11:e245-e249
Background Atypical electroencephalogram (EEG) abnormalities emerge in patients with subacute sclerosing panencephalitis (SSPE), especially in cases with an atypical clinical presentation that can lead to diagnostic difficulties. Case Report In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5e1a5d3bfee07d3e1c1dcdcf05e31af
https://doi.org/10.1055/s-0041-1735536
https://doi.org/10.1055/s-0041-1735536
Autor:
Albena Jordanova, Vanyo Mitev, Maria Bojidarova, Valentina Peycheva, Elena Rodopska, E Simeonov, N Ivanova, Petia Dimova, Dimitar Stamatov, Iliana Pacheva, Daniela Deneva, Margarita V. Panova, Veneta Bojinova, D. Hristova, Ivan Litvinenko, Iliyana Aleksandrova, Elena Slavkova, Kunka Kamenarova, Radka Kaneva, Ivan Ivanov, Genoveva Tacheva
Publikováno v:
Turkish journal of pediatrics
Background. Dravet syndrome (DS) is the most severe form of Generalized Epilepsy with Febrile Seizures plus (GEFS+) syndrome with a clear genetic component in 85% of the cases. It is characterized by fever-provoked seizure onset around six months of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24c32b717449e1f4137caa1fa64dec01
https://pubmed.ncbi.nlm.nih.gov/33108073
https://pubmed.ncbi.nlm.nih.gov/33108073