Serum Leptin Levels in Treatment-Naive Patients with Clinically Isolated Syndrome or Relapsing-Remitting Multiple Sclerosis

por Evangelopoulos, Maria Eleftheria, Koutsis, Georgios, Markianos, Manolis
Publicado 2014

Relapsing Remitting Multiple Sclerosis in X-Linked Charcot-Marie-Tooth Disease with Central Nervous System Involvement

por Koutsis, Georgios, Karadima, Georgia, Floroskoufi, Paraskewi, Raftopoulou, Maria, Panas, Marios
Publicado 2015

Body Mass Index in Multiple Sclerosis: Associations with CSF Neurotransmitter Metabolite Levels

por Markianos, Manolis, Evangelopoulos, Maria-Eleftheria, Koutsis, Georgios, Davaki, Panagiota, Sfagos, Constantinos
Publicado 2013

High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients

por Mok, Kin Y., Koutsis, Georgios, Schottlaender, Lucia V., Polke, James, Panas, Marios, Houlden, Henry
Publicado 2012

From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17

por Koutsis, Georgios, Panas, Marios, Paraskevas, George P., Bougea, Anastasia M., Kladi, Athina, Karadima, Georgia, Kapaki, Elisabeth
Publicado 2014

Thyroid Autoimmunity Following Alemtuzumab Treatment in Multiple Sclerosis Patients

por Kazakou, Paraskevi, Tzanetakos, Dimitrios, Vakrakou, Aigli G, Tzartos, John S, Anagnostouli, Maria, Koutsis, Georgios, Andreadou, Elisabeth, Evangelopoulos, Maria Eleptheria, Kilidireas, Constantinos, Zapanti, Evangelia
Publicado 2021

Multiple Sclerosis: Shall We Target CD33?

por Siokas, Vasileios, Tsouris, Zisis, Aloizou, Athina-Maria, Bakirtzis, Christos, Liampas, Ioannis, Koutsis, Georgios, Anagnostouli, Maria, Bogdanos, Dimitrios P., Grigoriadis, Nikolaos, Hadjigeorgiou, Georgios M., Dardiotis, Efthimios
Publicado 2020

Clinico-radiologic features and therapeutic strategies in tumefactive demyelination: a retrospective analysis of 50 consecutive cases

por Vakrakou, Aigli G., Tzanetakos, Dimitrios, Evangelopoulos, Maria-Eleptheria, Argyrakos, Theodore, Tzartos, John S., Anagnostouli, Maria, Andreadou, Elissavet, Koutsis, Georgios, Velonakis, Georgios, Toulas, Panagiotis, Gialafos, Elias, Dimitrakopoulos, Antonios, Psimenou, Erasmia, Stefanis, Leonidas, Kilidireas, Constantinos
Publicado 2021

Recurrent Fulminant Tumefactive Demyelination With Marburg-Like Features and Atypical Presentation: Therapeutic Dilemmas and Review of Literature

por Vakrakou, Aigli G., Tzanetakos, Dimitrios, Argyrakos, Theodore, Koutsis, Georgios, Evangelopoulos, Maria-Eleptheria, Andreadou, Elisabeth, Anagnostouli, Maria, Breza, Marianthi, Tzartos, John S., Gialafos, Elias, Dimitrakopoulos, Antonios N., Velonakis, Georgios, Toulas, Panagiotis, Stefanis, Leonidas, Kilidireas, Constantinos
Publicado 2020

High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes

por Tzagournissakis, Minas, Foukarakis, Emmanouil, Samonakis, Dimitrios, Tsilimbaris, Miltiadis, Michaelidou, Kleita, Mathioudakis, Lambros, Marinis, Anastasios, Giannakoudakis, Emmanouil, Spanaki, Cleanthe, Skoula, Irene, Erimaki, Sofia, Amoiridis, Georgios, Koutsis, Georgios, Koukouraki, Sofia, Stylianou, Kostas, Plaitakis, Andreas, Mitsias, Panayiotis D., Zaganas, Ioannis
Publicado 2022

Genotyping and Plasma/Cerebrospinal Fluid Profiling of a Cohort of Frontotemporal Dementia–Amyotrophic Lateral Sclerosis Patients

por Bourbouli, Mara, Paraskevas, George P., Rentzos, Mihail, Mathioudakis, Lambros, Zouvelou, Vasiliki, Bougea, Anastasia, Tychalas, Athanasios, Kimiskidis, Vasilios K., Constantinides, Vasilios, Zafeiris, Spiros, Tzagournissakis, Minas, Papadimas, Georgios, Karadima, Georgia, Koutsis, Georgios, Kroupis, Christos, Kartanou, Chrisoula, Kapaki, Elisabeth, Zaganas, Ioannis
Publicado 2021

Pure cerebellar ataxia due to bi‐allelic PRDX3 variants including recurring p.Asp202Asn

por Efthymiou, Stephanie, Novis, Luiz E., Koutsis, Georgios, Koniari, Chrysoula, Maroofian, Reza, Turchetti, Valentina, Velonakis, Georgios, Vasconcellos, Luiz F., Raskin, Salmo, Srinivasan, Varunvenkat M., Pagnamenta, Alistair T., Arun, Yaramanchanahalli B., Kinhal, Uddhava V., Gowda, Vykuntaraju K., Teive, Helio A. G., Houlden, Henry
Publicado 2023

A Greek National Cross-Sectional Study on Myotonic Dystrophies

por Papadimas, Georgios K., Papadopoulos, Constantinos, Kekou, Kyriaki, Kartanou, Chrisoula, Kladi, Athina, Nitsa, Evangelia, Sofocleous, Christalena, Tsanou, Evangelia, Sarmas, Ioannis, Kaninia, Stefania, Chroni, Elisabeth, Tsivgoulis, Georgios, Kimiskidis, Vasilios, Arnaoutoglou, Marianthi, Stefanis, Leonidas, Panas, Marios, Koutsis, Georgios, Karadima, Georgia, Traeger-Synodinos, Joanne
Publicado 2022

Spastic paraplegia preceding PSEN1‐related familial Alzheimer's disease

por Chelban, Viorica, Breza, Marianthi, Szaruga, Maria, Vandrovcova, Jana, Murphy, David, Lee, Chia‐Ju, Alikhwan, Sondos, Bourinaris, Thomas, Vavougios, George, Ilyas, Muhammad, Halim, Sobia Ahsan, Al‐Harrasi, Ahmed, Kartanou, Chrisoula, Ronald, Coras, Blumcke, Ingmar, Alexoudi, Athanasia, Gatzonis, Stylianos, Stefanis, Leonidas, Karadima, Georgia, Wood, Nicholas W., Chávez‐Gutiérrez, Lucía, Hardy, John, Houlden, Henry, Koutsis, Georgios
Publicado 2021

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases

por Bettencourt, Conceição, Hensman‐Moss, Davina, Flower, Michael, Wiethoff, Sarah, Brice, Alexis, Goizet, Cyril, Stevanin, Giovanni, Koutsis, Georgios, Karadima, Georgia, Panas, Marios, Yescas‐Gómez, Petra, García‐Velázquez, Lizbeth Esmeralda, Alonso‐Vilatela, María Elisa, Lima, Manuela, Raposo, Mafalda, Traynor, Bryan, Sweeney, Mary, Wood, Nicholas, Giunti, Paola, Durr, Alexandra, Holmans, Peter, Houlden, Henry, Tabrizi, Sarah J., Jones, Lesley
Publicado 2016