Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Georgios Papadimas"'
Autor:
Maria Judit Molnar, Léna Szabó, Oana Aurelia Vladacenco, Ana Maria Cobzaru, Talya Dor, Amir Dori, Georgios Papadimas, Lenka Juříková, Ivan Litvinenko, Ivailo Tournev, Craig Dixon
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Purpose An increasing number of patients with Duchenne muscular dystrophy (DMD) now have access to improved standard of care and disease modifying treatments, which improve the clinical course of DMD and extend life expectancy beyond 30 year
Externí odkaz:
https://doaj.org/article/c6442b257adc4302b77772db2cd5492e
Autor:
Marianna Papadopoulou, Dimitrios Tzanetakos, Christos Moschovos, Anastasia Korona, George Vartzelis, Konstantinos Voudris, Stella Fanouraki, Evangelia-Makrina Dimitriadou, Georgios Papadimas, John S. Tzartos, Sotirios Giannopoulos, Georgios Tsivgoulis
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 12, p 3604 (2024)
Background/Objectives: Myelin oligodendrocyte glycoprotein (MOG) is exclusively expressed in the central nervous system (CNS) and is found on the outer surface of oligodendrocytes. Antibodies to MOG are associated with CNS demyelination, whereas peri
Externí odkaz:
https://doaj.org/article/aae25eb571074d178e29af0ea063c684
Autor:
Mara Bourbouli, George P. Paraskevas, Mihail Rentzos, Lambros Mathioudakis, Vasiliki Zouvelou, Anastasia Bougea, Athanasios Tychalas, Vasilios K. Kimiskidis, Vasilios Constantinides, Spiros Zafeiris, Minas Tzagournissakis, Georgios Papadimas, Georgia Karadima, Georgios Koutsis, Christos Kroupis, Chrisoula Kartanou, Elisabeth Kapaki, Ioannis Zaganas
Publikováno v:
Brain Sciences, Vol 11, Iss 9, p 1239 (2021)
Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are part of the same pathophysiological spectrum and have common genetic and cerebrospinal fluid (CSF) biomarkers. Our aim here was to identify causative gene variants in a cohort
Externí odkaz:
https://doaj.org/article/0de80d7afbd44319a4bd62a31dc72b16
Autor:
Polyxeni Spiliopoulou, Gregory C. Bogdanis, Georgios Papadimas, Constantinos Papadopoulos, Gerasimos Terzis, Spyridon Methenitis, Nikolaos Zaras
Publikováno v:
Journal of Strength and Conditioning Research. 35:2464-2471
Spiliopoulou, P, Zaras, N, Methenitis, S, Papadimas, G, Papadopoulos, C, Bogdanis, GC, and Terzis, G. Effect of concurrent power training and high-intensity interval cycling on muscle morphology and performance. J Strength Cond Res 35(9): 2464-2471,
Autor:
Gerasimos Terzis, Eleni Kontou, Georgios Papadimas, Constantinos Papadopoulos, Argyro Krase, Ioannis Arnaoutis
Publikováno v:
International Journal of Neuroscience. 132:699-705
Pompe disease is a rare autosomal recessive disorder caused by the deficiency of acid α-glycosidase resulting in accumulation of glycogen in the lysosomes. The late-onset form of the disease (LOPD) causes primarily progressive muscle weakness and re
Autor:
Thomas Theodosiou, Foteini Christidi, Sofia Xirou, Efstratios Karavasilis, Peter Bede, Constantinos Papadopoulos, Georgios D. Argyropoulos, Panagiotis Kourtesis, Varvara Pantolewn, Panagiotis Ferentinos, Evangelia Kararizou, Georgios Velonakis, Ioannis Zalonis, Georgios Papadimas
Publikováno v:
Cognitive and Behavioral Neurology
Cognitive and Behavioral Neurology, 2022, Publish Ahead of Print, pp.1-27. ⟨10.1097/WNN.0000000000000314⟩
Cognitive and Behavioral Neurology, 2022, Publish Ahead of Print, pp.1-27. ⟨10.1097/WNN.0000000000000314⟩
In contrast to myotonic dystrophy type 1, the cognitive and radiologic profile of myotonic dystrophy type 2 (DM2) is relatively poorly characterized.To conduct a pilot study to systematically evaluate cognitive and radiologic features in a cohort of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e6d2b17bdfcd1f444091ff92cb6c6cf
https://inria.hal.science/hal-03764271/document
https://inria.hal.science/hal-03764271/document
Autor:
Nikos Karandreas, Vasilios C. Constantinides, Panagiotis Kokotis, Georgios Papadimas, Thomas Zambelis, Panagiota Manda, Maria Martha Papahatzaki
Publikováno v:
In Vivo. 32:1647-1652
Background/aim Diagnostic accuracy of muscle biopsy and electromyography (EMG) in patients with myopathy varies widely among studies. The goal of this study was to examine the diagnostic accuracy of each method in the diagnosis of patients with suspe
Publikováno v:
Journal of Neurology. 265:714-716
Autor:
Panagiota Manta, Thomas Zambelis, Nikolaos Karandreas, Georgios Papadimas, Vasiliki Zouvelou, Panagiotis Kokotis
Publikováno v:
International Journal of Neuroscience. :1-6
Purpose/aim of the study: An increased serum level of creatine kinase (CK) in asymptomatic individuals is a diagnostic challenge, as it may be associated with either physiological conditions, such as exercise or even signal an ominous neuromuscular d
Autor:
Evangelos Anagnostou, E. Kemanetzoglou, Evangelia Kararizou, Georgios Papadimas, Ioannis Evdokimidis
Publikováno v:
Neuromuscular Disorders. 24:1073-1078
Glycogen storage disease type II (Pompe disease) affects mainly proximal skeletal muscles. Despite older histological evidence of extraocular muscle involvement, ocular motor palsies or other eye movement abnormalities are not considered part of the