Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Iliana Pacheva"'
Autor:
Maria Gevezova, Zdravko Ivanov, Iliana Pacheva, Elena Timova, Maria Kazakova, Eleonora Kovacheva, Ivan Ivanov, Victoria Sarafian
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8211 (2024)
Autism spectrum disorder (ASD) is associated with multiple physiological abnormalities. Current laboratory and clinical evidence most commonly report mitochondrial dysfunction, oxidative stress, and immunological imbalance in almost every cell type o
Externí odkaz:
https://doaj.org/article/218213393ad44fa5b2e4bfc743bd11d2
Autor:
Maria Gevezova, Danail Minchev, Iliana Pacheva, Tatyana Todorova, Ralitsa Yordanova, Elena Timova, Ivan Ivanov, Victoria Sarafian
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11917 (2022)
Background: NGF is a molecule with a pleiotropic role, affecting neuro-immune functions, energy homeostasis, and synaptic plasticity. The mechanisms of NGF-induced neuronal differentiation are well established, but its effect on mitochondria in autis
Externí odkaz:
https://doaj.org/article/3bea9fbcc9c34105aea30f38df4ea08d
Autor:
Maya Atanasoska, Radoslava Vazharova, Ivan Ivanov, Lubomir Balabanski, Silvia Andonova, Samuil Ivanov, Iliana Pacheva, Maxim Malinov, Draga Toncheva
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 32, Iss 6, Pp 1345-1351 (2018)
Early infantile epileptic encephalopathy (EIEE) is a disorder with variable genetic heterogeneity. Symptoms are mostly presented with generalised epileptic seizures with an infantile onset and progressive neurodevelopmental delay. Early infantile epi
Externí odkaz:
https://doaj.org/article/55309ff54a6f4886821c7554ab69568d
Autor:
Maria Gevezova, Victoria Sarafian, Danail Minchev, Ivan Ivanov, Ralitsa Yordanova, Vasil Kotetarov, Yordan Sbirkov, Iliana Pacheva, Elena Timova
Publikováno v:
Current Topics in Medicinal Chemistry. 21:985-994
Background: Although Autism Spectrum Disorder (ASD) is considered a heterogeneous neurological disease in childhood, a growing body of evidence associates it with mitochondrial dysfunction explaining the observed comorbidities. Introduction: The aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87a9a3610f6227fbbeb8a9c82fae2e1d
https://doi.org/10.2174/1568026621666210521142131
https://doi.org/10.2174/1568026621666210521142131
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
Autor:
Radoslava Vazharova, Draga Toncheva, Iliana Pacheva, Samuil Ivanov, Maya Atanasoska, Silvia Andonova, Ivan Ivanov, Maxim Malinov, Lubomir Balabanski
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 32, Iss 6, Pp 1345-1351 (2018)
Early infantile epileptic encephalopathy (EIEE) is a disorder with variable genetic heterogeneity. Symptoms are mostly presented with generalised epileptic seizures with an infantile onset and progressive neurodevelopmental delay. Early infantile epi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::031d813ea099313b915b8a78e1b72cc4
https://doi.org/10.1080/13102818.2018.1532815
https://doi.org/10.1080/13102818.2018.1532815
Autor:
Daniela Avdjieva-Tzavella, Dimitar Stamatov, Sashka Zhelyazkova, Radka Kaneva, Iliana A Alexandrova, Iliana Pacheva, Ivan Litvinenko, Vanyo Mitev, E Simeonov, Veneta Bozhinova, Valentina Peycheva, Kunka Kamenarova, Neviana Ivanova, Petya Dimova, Ivan Ivanov, Ivailo Tournev, Albena Jordanova
Publikováno v:
Gene
High resolution chromosomal microarray analysis (CMA) has facilitated the identification of small chromosomal rearrangements throughout the genome, associated with various neurodevelopmental phenotypes, including ID/DD. Recently, it became evident th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c4dd58eb4a28f4aa0a26e13eae6bf6b
https://pubmed.ncbi.nlm.nih.gov/29753047
https://pubmed.ncbi.nlm.nih.gov/29753047
Autor:
Pasquale Striano, Edoardo Sessa, Pierre Genton, Tiziana Calarese, Edoardo Ferlazzo, Komi Assogba, Nathalie Villeneuve, Iliana Pacheva, Ivan Ivanov, Placido Bramanti
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 31(1)
Hypomelanosis of Ito (HI) is a rare neuroectodermal disorder often associated with mental retardation and epilepsy. We report on four new HI patients presenting with heterogeneous seizure manifestations and we review the literature concerning epilept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d53c5cf7f687bbcf2842db7dd46cc0e
https://pubmed.ncbi.nlm.nih.gov/19902142
https://pubmed.ncbi.nlm.nih.gov/19902142