Athanassiadou A - Search Results

1

Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson disease.

Voutsinas GE, Stavrou EF, Karousos G, Dasoula A, Papachatzopoulou A, Syrrou M, Verkerk AJ, van der Spek P, Patrinos GP, Stöger R, Athanassiadou A. Voutsinas GE, et al. Among authors: athanassiadou a. Hum Mutat. 2010 Jun;31(6):685-91. doi: 10.1002/humu.21248. Hum Mutat. 2010. PMID: 20340137

2

Detection and genetic analysis of beta-thalassemia mutations by competitive oligopriming.

Athanassiadou A, Papachatzopoulou A, Gibbs RA. Athanassiadou A, et al. Hum Mutat. 1995;6(1):30-5. doi: 10.1002/humu.1380060107. Hum Mutat. 1995. PMID: 7550228

3

A novel beta-thalassaemia mutation in the 5' untranslated region of the beta-globin gene.

Athanassiadou A, Papachatzopoulou A, Zoumbos N, Maniatis GM, Gibbs R. Athanassiadou A, et al. Br J Haematol. 1994 Oct;88(2):307-10. doi: 10.1111/j.1365-2141.1994.tb05023.x. Br J Haematol. 1994. PMID: 7803275

4

Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein.

Athanassiadou A, Voutsinas G, Psiouri L, Leroy E, Polymeropoulos MH, Ilias A, Maniatis GM, Papapetropoulos T. Athanassiadou A, et al. Am J Hum Genet. 1999 Aug;65(2):555-8. doi: 10.1086/302486. Am J Hum Genet. 1999. PMID: 10417297 Free PMC article. No abstract available.

5

Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease.

Papapetropoulos S, Paschalis C, Athanassiadou A, Papadimitriou A, Ellul J, Polymeropoulos MH, Papapetropoulos T. Papapetropoulos S, et al. Among authors: athanassiadou a. J Neurol Neurosurg Psychiatry. 2001 May;70(5):662-5. doi: 10.1136/jnnp.70.5.662. J Neurol Neurosurg Psychiatry. 2001. PMID: 11309462 Free PMC article.

6

Lack of Fas (APO-1/CD95) gene structural alterations or transcript variant ratio changes in breast cancer.

Puiu L, Petrakou E, Apostolidou A, Athanassiadou A, Psiouri L, Papachatzopoulou A, Gorgoulis VG, Kotsinas A, Tzoracoeleftherakis E, Maniatis GM, Voutsinas G. Puiu L, et al. Among authors: athanassiadou a. Cancer Lett. 2003 May 8;194(1):91-7. doi: 10.1016/s0304-3835(03)00049-1. Cancer Lett. 2003. PMID: 12706862

7

Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.

Papapetropoulos S, Ellul J, Paschalis C, Athanassiadou A, Papadimitriou A, Papapetropoulos T. Papapetropoulos S, et al. Among authors: athanassiadou a. Eur J Neurol. 2003 May;10(3):281-6. doi: 10.1046/j.1468-1331.2003.00576.x. Eur J Neurol. 2003. PMID: 12752402

8

Thalassaemia mutations within the 5'UTR of the human beta-globin gene disrupt transcription.

Sgourou A, Routledge S, Antoniou M, Papachatzopoulou A, Psiouri L, Athanassiadou A. Sgourou A, et al. Among authors: athanassiadou a. Br J Haematol. 2004 Mar;124(6):828-35. doi: 10.1111/j.1365-2141.2004.04835.x. Br J Haematol. 2004. PMID: 15009072 Free article.

9

Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.

Papachatzopoulou A, Kourakli A, Makropoulou P, Kakagianne T, Sgourou A, Papadakis M, Athanassiadou A. Papachatzopoulou A, et al. Among authors: athanassiadou a. Eur J Haematol. 2006 Apr;76(4):322-30. doi: 10.1111/j.1600-0609.2005.00618.x. Eur J Haematol. 2006. PMID: 16519704

10

The Ala53Thr mutation in the alpha-synuclein gene in a Korean family with Parkinson disease.

Ki CS, Stavrou EF, Davanos N, Lee WY, Chung EJ, Kim JY, Athanassiadou A. Ki CS, et al. Among authors: athanassiadou a. Clin Genet. 2007 May;71(5):471-3. doi: 10.1111/j.1399-0004.2007.00781.x. Clin Genet. 2007. PMID: 17489854 No abstract available.

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