Dardiotis E - Search Results

1

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: dardiotis e. Neurol Sci. 2010 Jun;31(3):253-7. doi: 10.1007/s10072-009-0155-2. Epub 2009 Oct 30. Neurol Sci. 2010. PMID: 19876593

2

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: dardiotis e. Eur J Radiol. 2004 Jun;50(3):278-84. doi: 10.1016/j.ejrad.2004.01.025. Eur J Radiol. 2004. PMID: 15145488

3

Re: Lack of association between the IL1A gene (-889) polymorphism and outcome after head injury. Tanriverdi T et al. Surg Neurol 2006;65:7-10; discussion 10.

Dardiotis E, Dardioti M, Hadjigeorgiou GM, Paterakis K. Dardiotis E, et al. Surg Neurol. 2006 Sep;66(3):334-5. doi: 10.1016/j.surneu.2006.05.042. Surg Neurol. 2006. PMID: 16935657 No abstract available.

4

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. Among authors: dardiotis e. J Orthop Res. 2007 Aug;25(8):1087-93. doi: 10.1002/jor.20393. J Orthop Res. 2007. PMID: 17469180 Free article.

5

Genetic association studies in osteonecrosis of the femoral head: mini review of the literature.

Hadjigeorgiou G, Dardiotis E, Dardioti M, Karantanas A, Dimitroulias A, Malizos K. Hadjigeorgiou G, et al. Among authors: dardiotis e. Skeletal Radiol. 2008 Jan;37(1):1-7. doi: 10.1007/s00256-007-0395-2. Skeletal Radiol. 2008. PMID: 17962936 Review. No abstract available.

6

Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.

Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, Ferrarese C, Hadjigeorgiou GM, Krueger R, Lambert JC, Lesage S, Markopoulou K, Mellick GD, Meeus B, Pedersen NL, Quattrone A, Van Broeckhoven C, Sharma M, Silburn PA, Tan EK, Wirdefeldt K, Ioannidis JP; Genetic Epidemiology of Parkinson's Disease (GEOPD) Consortium. Evangelou E, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):220-8. doi: 10.1002/ajmg.b.30980. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19475631 Free PMC article.

7

Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met.

Dardiotis E, Koutsou P, Zamba-Papanicolaou E, Vonta I, Hadjivassiliou M, Hadjigeorgiou G, Cariolou M, Christodoulou K, Kyriakides T. Dardiotis E, et al. J Neurol Sci. 2009 Sep 15;284(1-2):158-62. doi: 10.1016/j.jns.2009.05.018. Epub 2009 Jun 3. J Neurol Sci. 2009. PMID: 19493541

8

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.

Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage S, Lin JJ, Lynch T, Mellick GD, de Nigris F, Opala G, Prigione A, Quattrone A, Ross OA, Satake W, Silburn PA, Tan EK, Toda T, Tomiyama H, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Maraganore DM; Genetic Epidemiology of Parkinson's disease consortium. Krüger R, et al. Neurobiol Aging. 2011 Mar;32(3):548.e9-18. doi: 10.1016/j.neurobiolaging.2009.11.021. Epub 2009 Dec 24. Neurobiol Aging. 2011. PMID: 20036034 Free PMC article.

9

Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.

Tsironi EE, Pefkianaki M, Tsezou A, Kotoula MG, Dardiotis E, Almpanidou P, Papathanasiou AA, Rodopoulou P, Chatzoulis DZ, Hadjigeorgiou GM. Tsironi EE, et al. Among authors: dardiotis e. Mol Vis. 2009 Dec 25;15:2890-5. Mol Vis. 2009. PMID: 20038976 Free PMC article.

10

Genetic basis of Parkinson disease.

Xiromerisiou G, Dardiotis E, Tsimourtou V, Kountra PM, Paterakis KN, Kapsalaki EZ, Fountas KN, Hadjigeorgiou GM. Xiromerisiou G, et al. Among authors: dardiotis e. Neurosurg Focus. 2010 Jan;28(1):E7. doi: 10.3171/2009.10.FOCUS09220. Neurosurg Focus. 2010. PMID: 20043722

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