Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Pelagia Vorgia"'
Autor:
Danai Veltra, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Triantafyllia Tsaprouni, Roser Pons, Konstantina Kosma, Afroditi Kampouraki, Irene Tsoutsou, Periklis Makrythanasis, Kyriaki Kekou, Joanne Traeger-Synodinos, Christalena Sofocleous
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 5644 (2024)
SCN1A, the gene encoding for the Nav1.1 channel, exhibits dominant interneuron-specific expression, whereby variants disrupting the channel’s function affect the initiation and propagation of action potentials and neuronal excitability causing vari
Externí odkaz:
https://doaj.org/article/4aedc87e434a49f1a5e1f02528c3335a
Autor:
Christina Doxaki, Eleftheria Papadopoulou, Iliana Maniadaki, Nikolaos G. Tsakalis, Konstantinos Palikaras, Pelagia Vorgia
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Guillain-Barre Syndrome (GBS), a common cause of acute flaccid paralysis, is characterized by a rapidly progressive, usually symmetric weakness of the extremities. Headache and intracranial hypertension (ICHT) are very rare complications of GBS. Here
Externí odkaz:
https://doaj.org/article/8e3a2778feee4db8b9a079111bae0279
Autor:
Ioannis Zaganas, Pelagia Vorgia, Martha Spilioti, Lambros Mathioudakis, Maria Raissaki, Stavroula Ilia, Melpomeni Giorgi, Irene Skoula, Georgios Chinitrakis, Kleita Michaelidou, Evangelos Paraskevoulakos, Olga Grafakou, Chariklia Kariniotaki, Thekla Psyllou, Spiros Zafeiris, Maria Tzardi, George Briassoulis, Argirios Dinopoulos, Panayiotis Mitsias, Athanasios Evangeliou
Publikováno v:
Epilepsy & Behavior Reports, Vol 16, Iss , Pp 100477- (2021)
We describe a cohort of 10 unrelated Greek patients (4 females, 6 males; median age 6.5 years, range 2–18 years) with heterogeneous epilepsy syndromes with a genetic basis. In these patients, causative genetic variants, including two novel ones, we
Externí odkaz:
https://doaj.org/article/026665cfc5734e56b69f7bb105f0ecb5
Autor:
Christina, Kamari, Emmanouil, Galanakis, Maria, Raissaki, George, Briassoulis, Georgia, Vlachaki, Pelagia, Vorgia
Publikováno v:
Neurological Sciences. 44:343-345
Background Multiple sclerosis (MS) is a demyelinating disease of the central nervous system, rare during childhood. MS variations, like tumefactive MS and Balo concentric sclerosis, constitute puzzling to treat diagnostic dilemmas for pediatric patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da68741482e551cab9dc98f50dbdb7f4
https://doi.org/10.1007/s10072-022-06396-y
https://doi.org/10.1007/s10072-022-06396-y
Autor:
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M. Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger-Synodinos, Christalena Sofocleous
Genetics of epilepsy are highly heterogeneous and complex. Lesions detected involve genes encoding various types of channels, transcription factors, and other proteins implicated in numerous cellular processes, such as synaptogenesis. Consequently, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c7e76871eca36a992422ab57cba7f9
Autor:
Evridiki Patelarou, Georgia Dragoumanaki, Dimitra Sifaki-Pistolla, Athina Patelarou, Pelagia Vorgia
Publikováno v:
Health. 13:1222-1241
The origin of Developmental Coordination Disorder (DCD) has not been clarified yet. DCD is considered as a movement disorder that may strongly affect child’s Activities of Daily Living (ADL). Reliable evaluation tools for young DCD are importantly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80ab6daf270d39a1ed67429a61e08a94
https://doi.org/10.4236/health.2021.1311090
https://doi.org/10.4236/health.2021.1311090
Autor:
Maria Svingou, Argirios Dinopoulos, George Vartzelis, Nikolaos Diamantopoulos, Charalabos Kotsalis, George-Konstantinos Papadimas, Pelagia Vorgia, Vasiliki Koute, Constantinos Papadopoulos, Konstantinos Skiadas, Athanasios Evangeliou, Evangelos Pavlou, George Niotakis, Christalena Sofocleous, Evangelia Nitsa, Joanne Traeger-Synodinos, Marina Katsalouli, Antigoni Papavasiliou, Kyriaki Kekou, Iliada Nakou, George Konstantinidis, Konstantinos A. Voudris, Efstathia Katsarou, Georgios Tsivgoulis, Niki Mourtzi, Roser Pons, Sotiris Youroukos
Publikováno v:
Journal of Neuromuscular Diseases
Background: Promising genetic treatments targeting the molecular defect of severe early-onset genetic conditions are expected to dramatically improve patients’ quality of life and disease epidemiology. Spinal Muscular Atrophy (SMA), is one of these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9dc4c186852b2444ec0cd0b53a46c48
http://europepmc.org/articles/PMC7836056
http://europepmc.org/articles/PMC7836056
Autor:
Christina Kamari, Emmanouil Galanakis, Maria Raissaki, George Briassoulis, Georgia Vlachaki, Pelagia Vorgia
Publikováno v:
Neurological Sciences. 44:1137-1137
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::815a44c5defc356c3a3ed97c10b9af6d
https://doi.org/10.1007/s10072-022-06502-0
https://doi.org/10.1007/s10072-022-06502-0
Autor:
Pelagia Vorgia, Ioannis Zaganas, Georgios Chinitrakis, Athanasios Evangeliou, Panayiotis Mitsias, E. Paraskevoulakos, Argirios Dinopoulos, Kleita Michaelidou, George Briassoulis, Maria Raissaki, Martha Spilioti, Chariklia Kariniotaki, M. Giorgi, Olga Grafakou, Irene Skoula, Stavroula Ilia, Spiros Zafeiris, Thekla Psyllou, Lambros Mathioudakis, Maria Tzardi
Publikováno v:
Epilepsy & Behavior Reports, Vol 16, Iss, Pp 100477-(2021)
We describe a cohort of 10 unrelated Greek patients (4 females, 6 males; median age 6.5 years, range 2–18 years) with heterogeneous epilepsy syndromes with a genetic basis. In these patients, causative genetic variants, including two novel ones, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2738ce310dc212eb8f70bba1b4898aa8
http://www.sciencedirect.com/science/article/pii/S2589986421000514
http://www.sciencedirect.com/science/article/pii/S2589986421000514