Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Margarita Panova"'
Autor:
Margarita Panova, Iliyana Pacheva, Katerina Gaberova, Ralitsa Iordanova, Iglica Sotkova, Fani Galabova, Desislava Tartova, Diana Dimitrova-Popova, Ivan Ivanov
Publikováno v:
Folia Medica, Vol 65, Iss 3, Pp 420-426 (2023)
Introduction: Acute hemiparesis is an emergency of various etiologies and possible fatal outcome. Aim: The aim of this study was to determine the etiology, clinical manifestations, and prognosis of acute hemiparesis in childhood. Materials and method
Externí odkaz:
https://doaj.org/article/4daebfced369440cba3d39d62687c498
Autor:
Ivan Ivanov, Iliyana Pacheva, Elena Timova, Ralitsa Iordanova, Fani Galabova, Katerina Gaberova, Aneliya Petkova, Vasil Kotetarov, Margarita Panova, Nikolay Tonchev, Lauren Franz
Publikováno v:
Diagnostics, Vol 11, Iss 1, p 106 (2021)
Diagnosis of autism spectrum disorder (ASD) before the age of three years is a challenge. Analyzing the present practice may help reaching that goal. Aim: To investigate developmental abnormalities and diagnostic pathway of ASD patients in pediatric
Externí odkaz:
https://doaj.org/article/804676671b3640b8b2cd850ff99be1ac
Autor:
Iliyana Pacheva, Ivan Ivanov, Ralitsa Yordanova, Katerina Gaberova, Fani Galabova, Margarita Panova, Aneliya Petkova, Elena Timova, Iglika Sotkova
Publikováno v:
Children, Vol 6, Iss 2, p 15 (2019)
The comorbidity of autistic spectrum disorder (ASD) and epilepsy has been widely discussed but many questions still remain unanswered. The aim of this study was to establish the occurrence of epilepsy among children with ASD to define the type of epi
Externí odkaz:
https://doaj.org/article/edc33cf3fea645789a7612baf9e1bd1f
Autor:
Ivan Ivanov, Iliyana Pacheva, Ralitsa Yordanova, Iglika Sotkova, Fani Galabova, Katerina Gaberova, Margarita Panova, Ina Gheneva, Tsvetelina Tsvetanova, Katerina Noneva, Diana Dimitrova, Stoyan Markov, Nikolay Sapundzhiev, Stoyan Bichev, Alexey Savov
Publikováno v:
CNS & Neurological Disorders - Drug Targets. 22:207-214
Background: Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC) is a neurodegenerative disease with neurodevelopmental delay, motor, and speech regression, pronounced extrapyramidal syndrome, and sensory deficits due to TUBB4A mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b03946c77b900c77050785e4c8107784
https://doi.org/10.2174/1871527321666220221100704
https://doi.org/10.2174/1871527321666220221100704