Zobrazeno 1 - 10
of 131
pro vyhledávání: '"Eleni Zamba"'
Autor:
Anna Onisiforou, Christiana C. Christodoulou, Eleni Zamba-Papanicolaou, Panos Zanos, Polymnia Georgiou
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundThe hippocampus, vital for memory and learning, is among the first brain regions affected in Alzheimer’s Disease (AD) and exhibits adult neurogenesis. Women face twice the risk of developing AD compare to men, making it crucial to underst
Externí odkaz:
https://doaj.org/article/a638202230fa4d93a04b6162aef1be20
Autor:
Ellie Mitsi, Christiana C. Christodoulou, Paschalis Nicolaou, Kyproula Christodoulou, Eleni Zamba-Papanicolaou
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionAmyotrophic lateral sclerosis (ALS) is a devastating, uniformly lethal degenerative disease of motor neurons, presenting with relentlessly progressive muscle atrophy and weakness. The etiology of ALS remains unexplained for over 85% of al
Externí odkaz:
https://doaj.org/article/86909ac6b69045afadf858fbfe1a754e
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
BackgroundMotor symptoms are well-characterized in Parkinson’s disease (PD). However, non-motor symptoms, such as depression, are commonly observed and can appear up to 10 years before motor features, resulting in one-third of individuals being mis
Externí odkaz:
https://doaj.org/article/c5492d31e4fe46b991a9ed38305fddf9
Autor:
Apostolia Topaloudi, Pritesh Jain, Melanie B. Martinez, Josephine K. Bryant, Grace Reynolds, Zoi Zagoriti, George Lagoumintzis, Eleni Zamba-Papanicolaou, John Tzartos, Konstantinos Poulas, Kleopas A. Kleopa, Socrates Tzartos, Marianthi Georgitsi, Petros Drineas, Peristera Paschou
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionAutoimmune disorders (ADs) are a group of about 80 disorders that occur when self-attacking autoantibodies are produced due to failure in the self-tolerance mechanisms. ADs are polygenic disorders and associations with genes both in the h
Externí odkaz:
https://doaj.org/article/505eb28a4d704c04bb8d481cde71c396
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:
Andrea C. Kakouri, Christina Votsi, Anastasis Oulas, Paschalis Nicolaou, Massimo Aureli, Giulia Lunghi, Maura Samarani, Giacomo M. Compagnoni, Sabrina Salani, Alessio Di Fonzo, Thalis Christophides, George A. Tanteles, Eleni Zamba-Papanicolaou, Marios Pantzaris, George M. Spyrou, Kyproula Christodoulou
Publikováno v:
Cell & Bioscience, Vol 12, Iss 1, Pp 1-22 (2022)
Abstract Background Spastic ataxias (SAs) encompass a group of rare and severe neurodegenerative diseases, characterized by an overlap between ataxia and spastic paraplegia clinical features. They have been associated with pathogenic variants in a nu
Externí odkaz:
https://doaj.org/article/de99e0b0ac504981bfdd3b7a8d50c5f7
Autor:
Dimitris Sokratous, Charalambos C. Charalambous, Eleni Zamba Papanicolaou, Kyriaki Michailidou, Nikos Konstantinou
Publikováno v:
PLoS ONE, Vol 18, Iss 3 (2023)
Relapsing-remitting Multiple Sclerosis is the most common demyelinating neurodegenerative disease and is characterized by periods of relapses and generation of various motor symptoms. These symptoms are associated with the corticospinal tract integri
Externí odkaz:
https://doaj.org/article/f8e04d1461734ad59485f81674e1f379
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
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4873 (2023)
Huntington’s Disease (HD) is a progressive neurodegenerative disease caused by CAG repeat expansion in the huntingtin gene (HTT). The HTT gene was the first disease-associated gene mapped to a chromosome, but the pathophysiological mechanisms, gene
Externí odkaz:
https://doaj.org/article/71edab9861c241ab9590e288e5e5b268
Autor:
Christiana C. Christodoulou, Christiana A. Demetriou, Elena Philippou, Eleni Zamba Papanicolaou
Publikováno v:
Nutrients, Vol 15, Iss 5, p 1136 (2023)
Huntington’s disease (HD) is a rare progressive neurodegenerative disease characterised by autosomal dominant inheritance. The past decade saw a growing interest in the associations between the Mediterranean Diet (MD) and HD risk and outcomes. The
Externí odkaz:
https://doaj.org/article/7cecee1c1a4c430281c1d6c8e123ad35