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Page 1
High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus.
Acta Myol. 2009 Jul;28(1):24-6.
Acta Myol. 2009.
PMID: 19772192
Free PMC article.
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.
Neurol Sci. 2010 Jun;31(3):393-7. doi: 10.1007/s10072-009-0201-0. Epub 2009 Dec 2.
Neurol Sci. 2010.
PMID: 19953284
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TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders.
Speletas M, Liadaki K, Kalala F, Daiou C, Katodritou E, Mandala E, Korantzis I, Ritis K, Zintzaras E, Germenis AE.
Speletas M, et al. Among authors: daiou c.
Thromb Res. 2008;122(1):27-32. doi: 10.1016/j.thromres.2007.09.016. Epub 2007 Nov 14.
Thromb Res. 2008.
PMID: 17999935
No abstract available.
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Correlations of JAK2-V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders.
Speletas M, Katodritou E, Daiou C, Mandala E, Papadakis E, Kioumi A, Ritis K, Korantzis I.
Speletas M, et al. Among authors: daiou c.
Leuk Res. 2007 Aug;31(8):1053-62. doi: 10.1016/j.leukres.2006.09.005. Epub 2006 Oct 12.
Leuk Res. 2007.
PMID: 17045648
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Relationship between 5,10-methylenetetrahydrofolate reductase C677T gene polymorphism and methotrexate related toxicity in patients with autoimmune diseases receiving folic acid supplementation.
Speletas M, Papadopoulos N, Daiou C, Katodritou E, Pavlitou-Tsiontsi A, Galanopoulou V.
Speletas M, et al. Among authors: daiou c.
Ann Rheum Dis. 2005 Dec;64(12):1791-2. doi: 10.1136/ard.2005.037218.
Ann Rheum Dis. 2005.
PMID: 16284346
Free PMC article.
No abstract available.
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