Anastasakis A - Search Results

1

Mitral valve in hypertrophic cardiomyopathy: a three-dimensional transesophageal study.

Venieri E, Aggeli C, Anastasakis A, Sambatakou H, Stefanadis C, Tousoulis D. Venieri E, et al. Among authors: anastasakis a. Hellenic J Cardiol. 2021 Jan-Feb;62(1):29-34. doi: 10.1016/j.hjc.2019.04.004. Epub 2019 Apr 17. Hellenic J Cardiol. 2021. PMID: 31002876 Free article.

2

Impaired cerebral autoregulation in Fabry disease: A case-control study.

Palaiodimou L, Papagiannopoulou G, Bakola E, Papadopoulou M, Kokotis P, Moschovos C, Vrettou AR, Kapsia E, Petras D, Anastasakis A, Lionaki S, Vlachopoulos C, Boletis IN, Zompola C, Tsivgoulis G. Palaiodimou L, et al. Among authors: anastasakis a. J Neuroimaging. 2023 Jul-Aug;33(4):582-589. doi: 10.1111/jon.13111. Epub 2023 May 5. J Neuroimaging. 2023. PMID: 37147184

3

A truncating variant altering the extreme C-terminal region of desmoplakin (DSP) suggests the crucial functional role of the region: a case report study.

Pantou MP, Gourzi P, Vlagkouli V, Papatheodorou E, Tsoutsinos A, Nyktari E, Degiannis D, Anastasakis A. Pantou MP, et al. Among authors: anastasakis a. BMC Med Genomics. 2023 May 4;16(1):95. doi: 10.1186/s12920-023-01527-6. BMC Med Genomics. 2023. PMID: 37143080 Free PMC article.

4

D313Y Variant in Fabry Disease: A Systematic Review and Meta-analysis.

Palaiodimou L, Stefanou MI, Bakola E, Papadopoulou M, Kokotis P, Vrettou AR, Kapsia E, Petras D, Anastasakis A, Xifaras N, Karachaliou E, Touloumi G, Vlachopoulos C, Boletis IN, Giannopoulos S, Tsivgoulis G, Zompola C. Palaiodimou L, et al. Among authors: anastasakis a. Neurology. 2022 Nov 8;99(19):e2188-e2200. doi: 10.1212/WNL.0000000000201102. Neurology. 2022. PMID: 36344272

5

Subclinical skeletal muscle abnormalities in patients with hypertrophic cardiomyopathy and their relation to clinical characteristics.

Anastasakis A, Karandreas N, Stathis P, Rigopoulos A, Theopistou A, Sepp R, Elliott PM, Panagiotakos DB, Stefanadis C, Toutouzas P. Anastasakis A, et al. Int J Cardiol. 2003 Jun;89(2-3):249-56. doi: 10.1016/s0167-5273(02)00481-3. Int J Cardiol. 2003. PMID: 12767549

6

Phenotype reveals genotype in a Greek long QT syndrome family.

Anastasakis A, Kotta CM, Kyriakogonas S, Wollnik B, Theopistou A, Stefanadis C. Anastasakis A, et al. Europace. 2006 Apr;8(4):241-4. doi: 10.1093/europace/eul012. Epub 2006 Mar 16. Europace. 2006. PMID: 16627448

7

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.

Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, Zambartas C, Stefanadis C, McKenna WJ, Protonotarios N. Antoniades L, et al. Among authors: anastasakis a. Eur Heart J. 2006 Sep;27(18):2208-16. doi: 10.1093/eurheartj/ehl184. Epub 2006 Aug 7. Eur Heart J. 2006. PMID: 16893920

8

Prevention of sudden cardiac death in the young: targeted evaluation of those at risk.

Anastasakis A, McKenna W, Stefanadis C. Anastasakis A, et al. Hellenic J Cardiol. 2006 Sep-Oct;47(5):251-4. Hellenic J Cardiol. 2006. PMID: 17134059 Free article. No abstract available.

9

Naxos disease presenting with ventricular tachycardia and troponin elevation.

Lazaros G, Anastasakis A, Tsiachris D, Dilaveris P, Protonotarios N, Stefanadis C. Lazaros G, et al. Among authors: anastasakis a. Heart Vessels. 2009 Jan;24(1):63-5. doi: 10.1007/s00380-008-1082-5. Epub 2009 Jan 23. Heart Vessels. 2009. PMID: 19165571

10

Novel sodium channel SCN5A mutations in Brugada syndrome patients from Greece.

Kotta CM, Anastasakis A, Gatzoulis K, Manolis AS, Stefanadis C. Kotta CM, et al. Among authors: anastasakis a. Int J Cardiol. 2010 Nov 5;145(1):45-8. doi: 10.1016/j.ijcard.2009.03.134. Epub 2009 Apr 29. Int J Cardiol. 2010. PMID: 19406494

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