Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

Autor: Hadjigeorgiou George M, Papadimitriou Alexandros, Peuralinna Terhi, Dardiotis Euthimios, Hellström Olli, Gourbali Vanesa, Eerola Johanna, Xiromerisiou Georgia, Clarimon Jordi, Tienari Pentti J, Singleton Andrew B

Publikováno v: BMC Neurology, Vol 5, Iss 1, p 11 (2005)

Abstract Background Fibroblast growth factor 20 (FGF20) is a neurotrophic factor preferentially expressed in the substantia nigra of rat brain and could be involved in dopaminergic neurons survival. Recently, a strong genetic association has been fou

Externí odkaz: https://doaj.org/article/ca4df04356334289845923916958b52d

Molecular characterization of McArdle’s disease in two large Finnish families

Autor: Bruno, Claudio, Löfberg, Mervi, Tamburino, Lucia, Jänkälä, Heidi, Hadjigeorgiou, George M, Andreu, Antonio L, Shanske, Sara, Somer, Hannu, DiMauro, Salvatore ^*

Publikováno v: In Journal of the Neurological Sciences 1999 165(2):121-125

Positron emission tomography changes in PARK1 mutation.

Autor: Perani, Daniela, Garibotto, Valentina, Hadjigeorgiou, George M., Papadimitriou, Dimitra, Fazio, Ferruccio, Papadimitriou, Alexandros

Publikováno v: Movement Disorders; Jan2006, Vol. 21 Issue 1, p127-130, 4p

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.

Autor: 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.

Publikováno v: BMC Neurology; 2005, Vol. 5, p1-5, 5p, 2 Charts

Screening for the C9ORF72 expansion in Greek Huntington Disease phenocopies and controls and meta-analysis of current data.

Autor: Rikos D; University of Thessaly, University Hospital of Larissa, Neurology Department, Larissa, GR., Marogianni C; University of Thessaly, University Hospital of Larissa, Neurology Department, Larissa, GR., Provatas A; University of Thessaly, University Hospital of Larissa, Neurology Department, Larissa, GR., Bourinaris T; Department of Molecular Neuroscience Institute of Neurology, University College London, London, UK., Arnaoutoglou M; First Neurology Clinic, AHEPA Hospital, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, GR., Stathis P; Department of Neurology, Mediterraneo Hospital, Athens, GR., Patrinos GP; University of Patras School of Health Sciences, Department of Pharmacy, Patras, GR.; United Arab Emirates University, College of Medicine and Health Sciences, Department of Pathology, Al-Ain, AE.; United Arab Emirates University, Zayed Center of Health Sciences, Al-Ain, AE., Dardiotis E; University of Thessaly, University Hospital of Larissa, Neurology Department, Larissa, GR., Hadjigeorgiou GM; Department of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, Larissa, GR.; Department of Neurology, Medical School, University of Cyprus, Nicosia, CY., Xiromerisiou G; University of Thessaly, University Hospital of Larissa, Neurology Department, Larissa, GR.

Publikováno v: Tremor and other hyperkinetic movements (New York, N.Y.) [Tremor Other Hyperkinet Mov (N Y)] 2020 Jun 12; Vol. 10, pp. 5. Date of Electronic Publication: 2020 Jun 12.