Papadimitriou A - Search Results

1

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. Among authors: papadimitriou a. Eur J Radiol. 2004 Jun;50(3):278-84. doi: 10.1016/j.ejrad.2004.01.025. Eur J Radiol. 2004. PMID: 15145488

2

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. Among authors: papadimitriou a. Mov Disord. 2006 Apr;21(4):534-9. doi: 10.1002/mds.20752. Mov Disord. 2006. PMID: 16250025

3

Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms in Greek multiple sclerosis (MS) patients with bout-onset MS.

Aggelakis K, Zacharaki F, Dardiotis E, Xiromerisiou G, Tsimourtou V, Ralli S, Gkaraveli M, Bourpoulas D, Rodopoulou P, Papadimitriou A, Hadjigeorgiou G. Aggelakis K, et al. Among authors: papadimitriou a. Neurol Sci. 2010 Jun;31(3):253-7. doi: 10.1007/s10072-009-0155-2. Epub 2009 Oct 30. Neurol Sci. 2010. PMID: 19876593

4

Conjugate eye deviation as predictor of acute cortical and subcortical ischemic brain lesions.

Kaditis DG, Zintzaras E, Sali D, Kotoulas G, Papadimitriou A, Hadjigeorgiou GM. Kaditis DG, et al. Among authors: papadimitriou a. Clin Neurol Neurosurg. 2016 Apr;143:80-5. doi: 10.1016/j.clineuro.2016.02.011. Epub 2016 Feb 9. Clin Neurol Neurosurg. 2016. PMID: 26903074

5

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: papadimitriou a. 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.

6

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. Among authors: papadimitriou a. J Neurol Sci. 2002 Feb 15;194(1):83-6. doi: 10.1016/s0022-510x(01)00662-1. J Neurol Sci. 2002. PMID: 11809171

7

Val66Met polymorphism is associated with decreased likelihood for pediatric headache and migraine.

Koute V, Michalopoulou A, Siokas V, Aloizou AM, Rikos D, Bogdanos DP, Kontopoulos E, Grivea IN, Syrogiannopoulos GA, Papadimitriou A, Hadjigeorgiou GM, Dardiotis E. Koute V, et al. Among authors: papadimitriou a. Neurol Res. 2021 Sep;43(9):715-723. doi: 10.1080/01616412.2021.1922181. Epub 2021 May 17. Neurol Res. 2021. PMID: 34000980

8

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. Among authors: papadimitriou a. Neuromuscul Disord. 2002 Nov;12(9):824-7. doi: 10.1016/s0960-8966(02)00028-7. Neuromuscul Disord. 2002. PMID: 12398832 Clinical Trial.

9

Preoperative evaluation with FMRI of patients with intracranial gliomas.

Kapsalakis IZ, Kapsalaki EZ, Gotsis ED, Verganelakis D, Toulas P, Hadjigeorgiou G, Chung I, Fezoulidis I, Papadimitriou A, Robinson JS, Lee GP, Fountas KN. Kapsalakis IZ, et al. Among authors: papadimitriou a. Radiol Res Pract. 2012;2012:727810. doi: 10.1155/2012/727810. Epub 2012 Jul 12. Radiol Res Pract. 2012. PMID: 22848821 Free PMC article.

10

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: papadimitriou a. 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.

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