Zobrazeno 1 - 10
of 64
pro vyhledávání: '"George K, Papadimas"'
Autor:
Andrea C. Kakouri, Demetris Koutalianos, Andrie Koutsoulidou, Anastasis Oulas, Marios Tomazou, Nikoletta Nikolenko, Chris Turner, Andreas Roos, Anna Lusakowska, Katarzyna Janiszewska, George K. Papadimas, Constantinos Papadopoulos, Evangelia Kararizou, Eleni Zamba Papanicolaou, Grainne Gorman, Hanns Lochmüller, George M. Spyrou, Leonidas A. Phylactou
Publikováno v:
RNA Biology, Vol 19, Iss 1, Pp 507-518 (2022)
Muscular dystrophies are a group of rare and severe inherited disorders mainly affecting the muscle tissue. Duchene Muscular Dystrophy, Myotonic Dystrophy types 1 and 2, Limb Girdle Muscular Dystrophy and Facioscapulohumeral Muscular Dystrophy are so
Externí odkaz:
https://doaj.org/article/fce9b866c9544801aef48904f2cb8776
Autor:
Vassilis E. Papadopoulos, George K. Papadimas, Sofia Androudi, Maria Anagnostouli, Maria-Eleftheria Evangelopoulos
Publikováno v:
Brain Sciences, Vol 13, Iss 10, p 1361 (2023)
Antibodies to glutamic acid decarboxylase (GAD) have been predominantly associated with stiff-person syndrome (SPS), which is often accompanied by organ-specific autoimmune diseases, such as late-onset type 1 diabetes. Autoimmune retinal pathology in
Externí odkaz:
https://doaj.org/article/d50a3e1c54ec4f0a938759865cb4f343
Autor:
Demetris Koutalianos, Andrie Koutsoulidou, Chrystalla Mytidou, Andrea C. Kakouri, Anastasis Oulas, Marios Tomazou, Tassos C. Kyriakides, Marianna Prokopi, Konstantinos Kapnisis, Nikoletta Nikolenko, Chris Turner, Anna Lusakowska, Katarzyna Janiszewska, George K. Papadimas, Constantinos Papadopoulos, Evangelia Kararizou, George M. Spyrou, Geneviève Gourdon, Eleni Zamba Papanicolaou, Grainne Gorman, Andreas Anayiotos, Hanns Lochmüller, Leonidas A. Phylactou
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss , Pp 169-183 (2021)
Myotonic dystrophy type 1 (DM1) is the most common adult-onset muscular dystrophy, primarily characterized by muscle wasting and weakness. Many biomarkers already exist in the rapidly developing biomarker research field that aim to improve patients
Externí odkaz:
https://doaj.org/article/0df8908873d4446eb6c45e3b522382e8
Autor:
Constantinos Papadopoulos, Edoardo Malfatti, Corinne Métay, Boris Keren, Elodie Lejeune, Julien Buratti, Sophia Xirou, Margarita Chrysanthou-Piterou, George K. Papadimas
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 11181 (2023)
Desmin is a class III intermediate filament protein highly expressed in cardiac, smooth and striated muscle. Autosomal dominant or recessive mutations in the desmin gene (DES) result in a variety of diseases, including cardiomyopathies and myofibrill
Externí odkaz:
https://doaj.org/article/c18812ced03448fd9dc6f41ce21768e9
Publikováno v:
Frontiers in Neurology, Vol 12 (2022)
Externí odkaz:
https://doaj.org/article/f4e4d73d7ca643da9cb1a20fd90d8179
Autor:
Constantinos Papadopoulos, Edoardo Malfatti, Corinne Metay, Boris Keren, Elodie Lejeune, Julien Buratti, Sophia Xirou, Margarita Chrysanthou-Piterou, George K Papadimas
Desmin is a class III intermediate filament highly expressed in cardiac, smooth and striated muscle Autosomal dominant or recessive mutations in the desmin gene (DES) result in a variety of diseases, including cardiomyopathies and myofibrillar myopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1b3d3f40d7e19109fee81933446e4a0
https://doi.org/10.20944/preprints202305.0074.v1
https://doi.org/10.20944/preprints202305.0074.v1
Autor:
Varvara Pantoleon, Thomas Theodosiou, George K. Papadimas, Constantinos Papadopoulos, Peter Bede, Panagiotis Kourtesis, Foteini Christidi, Efstratios Karavasilis, Ioannis Zalonis, Sofia Xirou, Evangelia Kararizou
Publikováno v:
Cognitive and Behavioral Neurology. 34:1-10
Myotonic dystrophies (DMs) are hereditary, multisystem, slowly progressive myopathies. One of the systems they affect is the CNS. In contrast to the well-established cognitive profile of myotonic dystrophy type 1 (DM1), only a few studies have invest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c30bbe8c185e87c2030efc8a97c0e21f
https://doi.org/10.1097/wnn.0000000000000263
https://doi.org/10.1097/wnn.0000000000000263
Autor:
Evangelos Anagnostou, Sophia Xirou, Evangelia Kararizou, Leonidas Stefanis, Constantinos Papadopoulos, George K. Papadimas
Publikováno v:
Muscle & Nerve. 63:765-769
Introduction Spinal muscular atrophy (SMA) most prominently affects proximal limb and bulbar muscles. Despite older case descriptions, ocular motor neuron palsies or other oculomotor abnormalities are not considered part of the phenotype. Methods We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56feced5b0986fc1e9dfc7d3f1ed84f2
https://doi.org/10.1002/mus.27204
https://doi.org/10.1002/mus.27204
Autor:
Konstantinos Kapnisis, Leonidas A. Phylactou, George M. Spyrou, Geneviève Gourdon, George K. Papadimas, Chris Turner, Marianna Prokopi, Andreas S. Anayiotos, Anna Lusakowska, Hanns Lochmüller, Nikoletta Nikolenko, Demetris Koutalianos, Constantinos Papadopoulos, Chrystalla Mytidou, Anastasis Oulas, Tassos C. Kyriakides, Katarzyna Janiszewska, Grainne S. Gorman, Eleni Zamba Papanicolaou, Andrea C. Kakouri, Marios Tomazou, Andrie Koutsoulidou, Evangelia Kararizou
Publikováno v:
Molecular Therapy-Methods and Clinical Development
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 23, pp.169-183. ⟨10.1016/j.omtm.2021.09.007⟩
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss, Pp 169-183 (2021)
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 23, pp.169-183. ⟨10.1016/j.omtm.2021.09.007⟩
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss, Pp 169-183 (2021)
Myotonic dystrophy type 1 (DM1) is the most common adult-onset muscular dystrophy, primarily characterized by muscle wasting and weakness. Many biomarkers already exist in the rapidly developing biomarker research field that aim to improve patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8b23e128f936dd313386b4a8aca3c9
https://hal.sorbonne-universite.fr/hal-03408757/document
https://hal.sorbonne-universite.fr/hal-03408757/document
Autor:
Andrie Koutsoulidou, Tassos C Kyriakides, George K Papadimas, Yiolanda Christou, Evangelia Kararizou, Eleni Zamba Papanicolaou, Leonidas A Phylactou
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0125341 (2015)
The discovery of reliable and sensitive blood biomarkers is useful for the diagnosis, monitoring and potential future therapy of diseases. Recently, microRNAs (miRNAs) have been identified in blood circulation and might have the potential to be used
Externí odkaz:
https://doaj.org/article/ed3e66be361d44caa22683bd199b7b3f