Vlachaki E - Search Results

1

Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent.

Tampaki A, Theodoridou S, Apostolou C, Delaki EE, Vlachaki E. Tampaki A, et al. Among authors: vlachaki e. Hippokratia. 2020 Jan-Mar;24(1):43-45. Hippokratia. 2020. PMID: 33364739 Free PMC article.

2

Cyclosporine therapy during pregnancy in a patient with β-thalassemia major and autoimmune haemolytic anemia: a case report and review of the literature.

Agapidou A, Vlachaki E, Theodoridis T, Economou M, Perifanis V. Agapidou A, et al. Among authors: vlachaki e. Hippokratia. 2013 Jan;17(1):85-7. Hippokratia. 2013. PMID: 23935353 Free PMC article.

3

Laboratory investigation of platelet function in patients with thalassaemia.

Theodoridou S, Economou M, Vyzantiadis TA, Teli A, Vlachaki E, Neokleous N, Kargioti A, Vakalopoulou S, Garypidou V, Gombakis N, Papachristou F. Theodoridou S, et al. Among authors: vlachaki e. Acta Haematol. 2014;132(1):45-8. doi: 10.1159/000355817. Epub 2014 Jan 14. Acta Haematol. 2014. PMID: 24434633

4

Vitamin B12 Deficiency and Hemoglobin H Disease Early Misdiagnosed as Thrombotic Thrombocytopenic Purpura: A Series of Unfortunate Events.

Andreadis P, Theodoridou S, Pasakiotou M, Arapoglou S, Gigi E, Vetsiou E, Vlachaki E. Andreadis P, et al. Among authors: vlachaki e. Case Rep Hematol. 2015;2015:478151. doi: 10.1155/2015/478151. Epub 2015 Nov 2. Case Rep Hematol. 2015. PMID: 26609455 Free PMC article.

5

Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence.

Sousos N, Adamidou D, Klonizakis P, Agapidou A, Theodoridou S, Spanos G, Psarras K, Vetsiou E, Vyzantiadis TA, Vlachaki E. Sousos N, et al. Among authors: vlachaki e. Acta Haematol. 2017;137(3):175-182. doi: 10.1159/000463919. Epub 2017 Apr 12. Acta Haematol. 2017. PMID: 28399542

6

Hepatitis E in transfusion-dependent thalassaemia patients, in Greece: a single centre experience.

Klonizakis P, Gioula G, Exindari M, Apostolou C, Kotsiafti A, Vlachaki E. Klonizakis P, et al. Among authors: vlachaki e. Vox Sang. 2017 Oct;112(7):678-679. doi: 10.1111/vox.12572. Epub 2017 Sep 10. Vox Sang. 2017. PMID: 28891120

7

Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease.

Demosthenous C, Rizos G, Vlachaki E, Tzatzagou G, Gavra M. Demosthenous C, et al. Among authors: vlachaki e. Hippokratia. 2017 Jan-Mar;21(1):43-45. Hippokratia. 2017. PMID: 29904256 Free PMC article.

8

Compound Heterozygosity for Silent Cap +1570 (T>C) (HBB: c*96T>C), Codon 39 (C>T) (HBB: c.118C>T) and the Presence of ααα^anti-3.7/αα in Greece. A Case Presentation.

Theodoridou S, Vyzantiadis TA, Vlachaki E. Theodoridou S, et al. Among authors: vlachaki e. Hemoglobin. 2018 May;42(3):194-195. doi: 10.1080/03630269.2018.1495648. Epub 2018 Sep 12. Hemoglobin. 2018. PMID: 30205726

9

Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study.

Kolliopoulou A, Siamoglou S, John A, Sgourou A, Kourakli A, Symeonidis A, Vlachaki E, Chalkia P, Theodoridou S, Ali BR, Katsila T, Patrinos GP, Papachatzopoulou A. Kolliopoulou A, et al. Among authors: vlachaki e. Hemoglobin. 2019 Jan;43(1):27-33. doi: 10.1080/03630269.2019.1597732. Epub 2019 Apr 30. Hemoglobin. 2019. PMID: 31039620

10

Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece.

Theodoridou S, Balassopoulou A, Boutou E, Delaki EE, Yfanti E, Vyzantiadis TA, Vetsiou E, Voskaridou E, Vlachaki E. Theodoridou S, et al. Among authors: vlachaki e. J Pediatr Hematol Oncol. 2020 Nov;42(8):e762-e764. doi: 10.1097/MPH.0000000000001730. J Pediatr Hematol Oncol. 2020. PMID: 32032239

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