Hadjigeorgiou GM - Search Results

1

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene.

Daiou C, Christodoulou K, Xiromerisiou G, Panas M, Dardiotis E, Kladi A, Speletas M, Ntaios G, Papadimitriou A, Germenis A, Hadjigeorgiou GM. Daiou C, et al. Among authors: hadjigeorgiou gm. Neurol Sci. 2010 Jun;31(3):393-7. doi: 10.1007/s10072-009-0201-0. Epub 2009 Dec 2. Neurol Sci. 2010. PMID: 19953284

2

Continuous muscle fiber activity associated with morphea (localized scleroderma).

Papadimitriou A, Chroni E, Anastasopoulos I, Avramidis T, Hadjigeorgiou G, Koutroumanidis M. Papadimitriou A, et al. Neurology. 1998 Dec;51(6):1763-4. doi: 10.1212/wnl.51.6.1763. Neurology. 1998. PMID: 9855545 No abstract available.

3

A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's disease.

Hadjigeorgiou GM, Papadimitriou A, Musumeci O, Paterakis K, Flabouriari K, Shanske S, DiMauro S. Hadjigeorgiou GM, et al. J Neurol Sci. 2002 Feb 15;194(1):83-6. doi: 10.1016/s0022-510x(01)00662-1. J Neurol Sci. 2002. PMID: 11809171

4

Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families.

Hadjigeorgiou GM, Sadeh M, Musumeci O, Dabby R, De Girolami L, Naini A, Papadimitriou A, Shanske S, DiMauro S. Hadjigeorgiou GM, et al. Neuromuscul Disord. 2002 Nov;12(9):824-7. doi: 10.1016/s0960-8966(02)00028-7. Neuromuscul Disord. 2002. PMID: 12398832 Clinical Trial.

5

Increased frequency of white matter lesions in patients with osteonecrosis (WMLeOn) of the femoral head.

Hadjigeorgiou GM, Karantanas AH, Zibis A, Dardiotis E, Aggelakis K, Papadimitriou A, Malizos K. Hadjigeorgiou GM, et al. Eur J Radiol. 2004 Jun;50(3):278-84. doi: 10.1016/j.ejrad.2004.01.025. Eur J Radiol. 2004. PMID: 15145488

6

Association of alpha-synuclein Rep1 polymorphism and Parkinson's disease: influence of Rep1 on age at onset.

Hadjigeorgiou GM, Xiromerisiou G, Gourbali V, Aggelakis K, Scarmeas N, Papadimitriou A, Singleton A. Hadjigeorgiou GM, et al. Mov Disord. 2006 Apr;21(4):534-9. doi: 10.1002/mds.20752. Mov Disord. 2006. PMID: 16250025

7

Absence of linkage to chromosomes 6q and 16p in a Greek population with knee osteoarthritis.

Tsezou A, Karachalios T, Fytili P, Giannatou E, Christodoulou K, Hadjigeorgiou GM, Malizos KN. Tsezou A, et al. Among authors: hadjigeorgiou gm. J Orthop Res. 2006 Sep;24(9):1900-5. doi: 10.1002/jor.20236. J Orthop Res. 2006. PMID: 16865722 Free article.

8

Autoantibodies to alpha-synuclein in inherited Parkinson's disease.

Papachroni KK, Ninkina N, Papapanagiotou A, Hadjigeorgiou GM, Xiromerisiou G, Papadimitriou A, Kalofoutis A, Buchman VL. Papachroni KK, et al. Among authors: hadjigeorgiou gm. J Neurochem. 2007 May;101(3):749-56. doi: 10.1111/j.1471-4159.2006.04365.x. J Neurochem. 2007. PMID: 17448146 Free PMC article.

9

Paraoxonase 1 gene polymorphisms in patients with osteonecrosis of the femoral head with and without cerebral white matter lesions.

Hadjigeorgiou GM, Malizos K, Dardiotis E, Aggelakis K, Dardioti M, Zibis A, Dimitroulias A, Scarmeas N, Tsezou A, Karantanas A. Hadjigeorgiou GM, et al. J Orthop Res. 2007 Aug;25(8):1087-93. doi: 10.1002/jor.20393. J Orthop Res. 2007. PMID: 17469180 Free article.

10

Association between AKT1 gene and Parkinson's disease: a protective haplotype.

Xiromerisiou G, Hadjigeorgiou GM, Papadimitriou A, Katsarogiannis E, Gourbali V, Singleton AB. Xiromerisiou G, et al. Among authors: hadjigeorgiou gm. Neurosci Lett. 2008 May 9;436(2):232-4. doi: 10.1016/j.neulet.2008.03.026. Epub 2008 Mar 15. Neurosci Lett. 2008. PMID: 18395980 Free PMC article.

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