Papadimitriou A - 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: papadimitriou a. 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

Mutated alpha-synuclein gene in two Greek kindreds with familial PD: incomplete penetrance?

Papadimitriou A, Veletza V, Hadjigeorgiou GM, Patrikiou A, Hirano M, Anastasopoulos I. Papadimitriou A, et al. Neurology. 1999 Feb;52(3):651-4. doi: 10.1212/wnl.52.3.651. Neurology. 1999. PMID: 10025809

3

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants.

Xiromerisiou G, Hadjigeorgiou GM, Gourbali V, Johnson J, Papakonstantinou I, Papadimitriou A, Singleton AB. Xiromerisiou G, et al. Among authors: papadimitriou a. Eur J Neurol. 2007 Jan;14(1):7-11. doi: 10.1111/j.1468-1331.2006.01551.x. Eur J Neurol. 2007. PMID: 17222106

4

Alpha-1 antichymotrypsin gene signal peptide a/t polymorphism and primary intracerebral hemorrhage.

Dardiotis E, Hadjigeorgiou GM, Dardioti M, Scarmeas N, Paterakis K, Aggelakis K, Komnos A, Tasiou A, Xiromerisiou G, Gabranis I, Zintzaras E, Papadimitriou A, Karantanas A. Dardiotis E, et al. Among authors: papadimitriou a. Eur Neurol. 2008;59(6):307-14. doi: 10.1159/000121420. Epub 2008 Apr 11. Eur Neurol. 2008. PMID: 18408372

5

IL-1RN and IL-1B gene polymorphisms and cerebral hemorrhagic events after traumatic brain injury.

Hadjigeorgiou GM, Paterakis K, Dardiotis E, Dardioti M, Aggelakis K, Tasiou A, Xiromerisiou G, Komnos A, Zintzaras E, Scarmeas N, Papadimitriou A, Karantanas A. Hadjigeorgiou GM, et al. Among authors: papadimitriou a. Neurology. 2005 Oct 11;65(7):1077-82. doi: 10.1212/01.wnl.0000178890.93795.0e. Neurology. 2005. PMID: 16217062

6

Genetic assessment of familial and early-onset Parkinson's disease in a Greek population.

Bozi M, Papadimitriou D, Antonellou R, Moraitou M, Maniati M, Vassilatis DK, Papageorgiou SG, Leonardos A, Tagaris G, Malamis G, Theofilopoulos D, Kamakari S, Stamboulis E, Hadjigeorgiou GM, Athanassiadou A, Michelakakis H, Papadimitriou A, Gasser T, Stefanis L. Bozi M, et al. Among authors: papadimitriou d, papadimitriou a. Eur J Neurol. 2014 Jul;21(7):963-8. doi: 10.1111/ene.12315. Epub 2013 Dec 7. Eur J Neurol. 2014. PMID: 24313877

7

Association of tumor necrosis factor-α gene polymorphism (-308) and obstructive sleep apnea-hypopnea syndrome.

Almpanidou P, Hadjigeorgiou G, Gourgoulianis K, Papadimitriou A. Almpanidou P, et al. Among authors: papadimitriou a. Hippokratia. 2012 Jul;16(3):217-20. Hippokratia. 2012. PMID: 23935286 Free PMC article.

8

Protein misfolding in neurodegenerative diseases.

Agorogiannis EI, Agorogiannis GI, Papadimitriou A, Hadjigeorgiou GM. Agorogiannis EI, et al. Among authors: papadimitriou a. Neuropathol Appl Neurobiol. 2004 Jun;30(3):215-24. doi: 10.1111/j.1365-2990.2004.00558.x. Neuropathol Appl Neurobiol. 2004. PMID: 15175075 Review.

9

Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts.

Fung HC, Xiromerisiou G, Gibbs JR, Wu YR, Eerola J, Gourbali V, Hellström O, Chen CM, Duckworth J, Papadimitriou A, Tienari PJ, Hadjigeorgiou GM, Hardy J, Singleton AB. Fung HC, et al. Among authors: papadimitriou a. Neurodegener Dis. 2006;3(6):327-33. doi: 10.1159/000097301. Neurodegener Dis. 2006. PMID: 17192721

10

The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism.

Papadimitriou A, Hadjigeorgiou GM, Divari R, Papagalanis N, Comi G, Bresolin N. Papadimitriou A, et al. Neuromuscul Disord. 1996 Jan;6(1):49-53. doi: 10.1016/0960-8966(95)00020-8. Neuromuscul Disord. 1996. PMID: 8845718

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