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Published in Clinical therapeutics (01.02.2010)
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Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients
Clarimon, Jordi, Xiromerisiou, Georgia, Eerola, Johanna, Gourbali, Vanesa, Hellström, Olli, Dardiotis, Euthimios, Peuralinna, Terhi, Papadimitriou, Alexandros, Hadjigeorgiou, George M, Tienari, Pentti J, Singleton, Andrew B
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Published in BMC neurology (20.06.2005)
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Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset
PLAITAKIS, Andreas, LATSOUDIS, Helen, XIROMERISIOU, Georgia, HADJIGEORGIOU, George M, SPANAKI, Cleanthe, KANAVOURAS, Konstantinos, RITZ, Beate, BRONSTEIN, Jeff M, SKOULA, Irene, MASTORODEMOS, Vasileios, PAPAPETROPOULOS, Spyridon, BOROMPOKAS, Nikolas, ZAGANAS, Ioannis
Published in European journal of human genetics : EJHG (01.03.2010)
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Screening for the C9ORF72 expansion in Greek Huntington Disease phenocopies and controls and meta-analysis of current data
Rikos, Dimitrios, Marogianni, Chrysoula, Provatas, Antonios, Bourinaris, Thomas, Arnaoutoglou, Marianthi, Stathis, Pantelis, Patrinos, George P, Dardiotis, Efthimios, Hadjigeorgiou, George M, Xiromerisiou, Georgia
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Depressive Symptoms in Alzheimer's Disease: Natural Course and Temporal Relation to Function and Cognitive Status
Holtzer, Roee, Scarmeas, Nikolaos, Wegesin, Domonick J., Albert, Marilyn, Brandt, Jason, Dubois, Bruno, Hadjigeorgiou, George M., Stern, Yaakov
Published in Journal of the American Geriatrics Society (JAGS) (01.12.2005)
Published in Journal of the American Geriatrics Society (JAGS) (01.12.2005)
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A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethality
CRIMI, Marco, PAPADIMITRIOU, Alexandros, BRESOLIN, Nereo, COMI, Giacomo Pietro, GALBIATI, Sara, PALAMIDOU, Phani, FORTUNATO, Francesco, BORDONI, Andreina, PAPANDREOU, Urania, PAPADIMITRIOU, Dimitra, HADJIGEORGIOU, George M, DROGARI, Eurydiki
Published in Pediatric research (01.05.2004)
Published in Pediatric research (01.05.2004)
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Molecular characterization of McArdle’s disease in two large Finnish families
Bruno, Claudio, Löfberg, Mervi, Tamburino, Lucia, Jänkälä, Heidi, Hadjigeorgiou, George M, Andreu, Antonio L, Shanske, Sara, Somer, Hannu, DiMauro, Salvatore
Published in Journal of the neurological sciences (01.06.1999)
Published in Journal of the neurological sciences (01.06.1999)
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Positron emission tomography changes in PARK1 mutation
Perani, Daniela, Garibotto, Valentina, Hadjigeorgiou, George M., Papadimitriou, Dimitra, Fazio, Ferruccio, Papadimitriou, Alexandros
Published in Movement disorders (01.01.2006)
Published in Movement disorders (01.01.2006)
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Psychological distress, personality traits and functional disability in patients with osteonecrosis of the femoral head
Mouzas, Odysseas D, Zibis, Aristidis H, Bonotis, Konstantinos S, Katsimagklis, Crysanthos D, Hadjigeorgiou, George M, Papaliaga, Maria N, Dimitroulias, Apostolos P, Malizos, Konstantinos N
Published in Journal of clinical medicine research (01.10.2014)
Published in Journal of clinical medicine research (01.10.2014)
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A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease
Bruno, Claudio, Tamburino, Lucia, Kawashima, Noriko, Andreu, Antonio L., Shanske, Sara, Hadjigeorgiou, George M., Kawashima, Atsushi, DiMauro, Salvatore
Published in Neuromuscular disorders : NMD (1999)
Published in Neuromuscular disorders : NMD (1999)
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