Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing von Lynch, David S, Koutsis, Georgios, Tucci, Arianna, Panas, Marios, Baklou, Markella, Breza, Marianthi, Karadima, Georgia, Houlden, Henry

Volltext

A Greek National Cross-Sectional Study on Myotonic Dystrophies von 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

Volltext

Replication study of GWAS risk loci in Greek multiple sclerosis patients von Hadjigeorgiou, Georgios M., Kountra, Persia-Maria, Koutsis, Georgios, Tsimourtou, Vana, Siokas, Vasileios, Dardioti, Maria, Rikos, Dimitrios, Marogianni, Chrysoula, Aloizou, Athina-Maria, Karadima, Georgia, Ralli, Styliani, Grigoriadis, Nikolaos, Bogdanos, Dimitrios, Panas, Marios, Dardiotis, Efthimios

Volltext

Relapsing Remitting Multiple Sclerosis in X-Linked Charcot-Marie-Tooth Disease with Central Nervous System Involvement von Raftopoulou, Maria, Floroskoufi, Paraskewi, Karadima, Georgia, Koutsis, Georgios, Panas, Marios

Volltext

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population von Koutsis, Georgios, Karadima, Georgia, Kartanou, Chrisoula, Kladi, Athina, Panas, Marios

Volltext

Elevated Serum α-Synuclein Levels in Huntington’s Disease Patients von Breza, Marianthi, Emmanouilidou, Evangelia, Leandrou, Emmanouela, Kartanou, Chrisoula, Bougea, Anastasia, Panas, Marios, Stefanis, Leonidas, Karadima, Georgia, Vekrellis, Kostas, Koutsis, Georgios

Volltext

Evidence for Cognitive Deficits in X-Linked Charcot-Marie-Tooth Disease von Kasselimis, Dimitrios, Karadima, Georgia, Angelopoulou, Georgia, Breza, Marianthi, Tsolakopoulos, Dimitrios, Potagas, Constantin, Panas, Marios, Koutsis, Georgios

Volltext

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

Volltext

Association of genetically proven Huntington's disease and sporadic amyotrophic lateral sclerosis in a 72-year-old woman von PAPAGEORGIOU, Sokratis G, ANTELLI, Alexandra, BONAKIS, Anastasios, VASSOS, Evangelos, ZALONIS, Ioannis, KALFAKIS, Nikolaos, PANAS, Marios

Volltext

Screening for the FMR1 premutation in Greek patients with late-onset movement disorders von Kartanou, Chrisoula, Seferiadi, Maria, Pomoni, Stella, Potagas, Constantin, Sofocleous, Chrystalena, Traeger-Synodinos, Joanne, Stefanis, Leonidas, Panas, Marios, Koutsis, Georgios, Karadima, Georgia

Volltext

From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17 von Kapaki, Elisabeth, Kladi, Athina, Bougea, A., Paraskevas, George P., Panas, Marios, Koutsis, Georgios, Karadima, Georgia

Volltext

Late-onset Huntington's disease: Diagnostic and prognostic considerations von Koutsis, Georgios, Karadima, Georgia, Kladi, Athina, Panas, Marios

Volltext

Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation von Kontogeorgiou, Zoi, Kartanou, Chrisoula, Rentzos, Michail, Kokotis, Panagiotis, Anagnostou, Evangelos, Zambelis, Thomas, Chroni, Elisabeth, Dinopoulos, Argyris, Panas, Marios, Koutsis, Georgios, Karadima, Georgia

Volltext

HINT1‐related neuropathy in Greek patients with Charcot‐Marie‐Tooth disease von Kontogeorgiou, Zoi, Voudommatis, Charalampos, Kartanou, Chrisoula, Pandis, Dionysis, Breza, Marianthi, Zambelis, Thomas, Stefanis, Leonidas, Panas, Marios, Koutsis, Georgios, Karadima, Georgia

Volltext

Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population von Kartanou, Chrisoula, Kontogeorgiou, Zoi, Rentzos, Michail, Potagas, Constantin, Aristeidou, Stavroula, Kapaki, Elisabeth, Paraskevas, George P, Constantinides, Vasilios C, Stefanis, Leonidas, Papageorgiou, Sokratis G, Houlden, Henry, Panas, Marios, Koutsis, Georgios, Karadima, Georgia

Volltext

Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms von Koutsis, Georgios, Kartanou, Chrisoula, Kontogeorgiou, Zoi, Koniari, Chrysoula, Mitrousias, Alexandros, Pellerin, David, Dicaire, Marie-Jose, Iruzubieta, Pablo, Danzi, Matt C., Athanassopoulos, Konstantinos, Ragazos, Nikolaos, Stamelou, Maria, Rentzos, Michail, Anagnostou, Evangelos, Zuchner, Stephan, Brais, Bernard, Houlden, Henry, Panas, Marios, Stefanis, Leonidas, Karadima, Georgia

Volltext

Mutational screening of the SH3TC2 gene in Greek patients with suspected demyelinating recessive Charcot‐Marie‐Tooth disease reveals a varied and unusual phenotypic spectrum von Kontogeorgiou, Zoi, Nikolaou, Katerina, Kartanou, Chrisoula, Breza, Marianthi, Panas, Marios, Karadima, Georgia, Koutsis, Georgios

Volltext

The FGF14 GAA repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the SCA27B phenotype across populations von Kartanou, Chrisoula, Mitrousias, Alexandros, Pellerin, David, Kontogeorgiou, Zoi, Iruzubieta, Pablo, Dicaire, Marie‐Josée, Danzi, Matt C., Koniari, Chrysoula, Athanassopoulos, Konstantinos, Panas, Marios, Stefanis, Leonidas, Zuchner, Stephan, Brais, Bernard, Houlden, Henry, Karadima, Georgia, Koutsis, Georgios

Volltext

The challenge of juvenile Huntington disease: To test or not to test von KOUTSIS, Georgios, KARADIMA, Georgia, KLADI, Athina, PANAS, Marios

Volltext

Spinobulbar muscular atrophy (Kennedy's disease): A rare diagnosis in the Greek population von Koutsis, Georgios, Kladi, Athina, Breza, Marianthi, Karadima, Georgia, Panas, Marios

Volltext