Georgiou I - Search Results

1

Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M. Pavlou E, et al. Among authors: georgiou i. Hemoglobin. 2006;30(4):455-62. doi: 10.1080/03630260600868006. Hemoglobin. 2006. PMID: 16987800

2

Distribution and frequency of beta-thalassemia mutations in northwestern and central Greece.

Georgiou I, Makis A, Chaidos A, Bouba I, Hatzi E, Kranas V, Zilidis C, Bourantas KL. Georgiou I, et al. Eur J Haematol. 2003 Feb;70(2):75-8. doi: 10.1034/j.1600-0609.2003.00017.x. Eur J Haematol. 2003. PMID: 12581187

3

A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family.

Makis A, Georgiou I, Traeger-Synodinos J, Storino MR, Giuliano M, Andolfo I, Hatzimichael E, Chaliasos N, Giapros V, Izzo P, Iolascon A, Grosso M. Makis A, et al. Among authors: georgiou i. Hemoglobin. 2021 Nov;45(6):351-354. doi: 10.1080/03630269.2019.1699568. Epub 2019 Dec 12. Hemoglobin. 2021. PMID: 31829079

4

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

Patsalis PC, Sismani C, Hettinger JA, Boumba I, Georgiou I, Stylianidou G, Anastasiadou V, Koukoulli R, Pagoulatos G, Syrrou M. Patsalis PC, et al. Among authors: georgiou i. Am J Med Genet. 1999 May 28;84(3):184-90. Am J Med Genet. 1999. PMID: 10331587

5

Non-invasive first-trimester detection of paternal beta-globin gene mutations and polymorphisms as predictors of thalassemia risk at chorionic villous sampling.

Lazaros L, Hatzi E, Bouba I, Makrydimas G, Dalkalitsis N, Stefos T, Paraskevaidis E, Georgiou I. Lazaros L, et al. Among authors: georgiou i. Eur J Obstet Gynecol Reprod Biol. 2008 Sep;140(1):17-20. doi: 10.1016/j.ejogrb.2007.12.019. Epub 2008 Mar 18. Eur J Obstet Gynecol Reprod Biol. 2008. PMID: 18353524

6

Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical Implications.

Zioga A, Thanopoulou E, Hatzi E, Chaliasos N, Georgiou I, Makis A. Zioga A, et al. Among authors: georgiou i. Hemoglobin. 2018 Sep-Nov;42(5-6):336-338. doi: 10.1080/03630269.2018.1558066. Epub 2019 Jan 9. Hemoglobin. 2018. PMID: 30626242

7

Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families.

Bouba I, Koptides M, Mean R, Costi CE, Demetriou K, Georgiou I, Pierides A, Siamopoulos K, Deltas CC. Bouba I, et al. Among authors: georgiou i. Eur J Hum Genet. 2001 Sep;9(9):677-84. doi: 10.1038/sj.ejhg.5200696. Eur J Hum Genet. 2001. PMID: 11571556

8

Molecular and Clinical Investigation of Cystinuria in the Greek-Cypriot Population.

Athanasiou Y, Voskarides K, Chatzikyriakidou A, Ignatiou A, Demosthenous P, Elia A, Zavros M, Georgiou I, Pierides A, Deltas C. Athanasiou Y, et al. Among authors: georgiou i. Genet Test Mol Biomarkers. 2015 Nov;19(11):641-5. doi: 10.1089/gtmb.2015.0144. Epub 2015 Nov 5. Genet Test Mol Biomarkers. 2015. PMID: 26540609

9

Diagnosis and molecular characterization of a novel α⁰ -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia.

Makis A, Georgiou I, Traeger-Synodinos J, Chaliasos N, Grosso M, Gambale A, Iolascon A. Makis A, et al. Among authors: georgiou i. Int J Lab Hematol. 2017 Oct;39(5):e124-e126. doi: 10.1111/ijlh.12690. Epub 2017 Jun 12. Int J Lab Hematol. 2017. PMID: 28603861 No abstract available.

10

Gamma-chain heterogeneity in Greek (delta beta)zero-thalassemia.

Georgiou I, Seferiadis K, Lolis D, Tsolas O, Bourantas KL. Georgiou I, et al. Eur J Haematol. 1995 Feb;54(2):101-5. Eur J Haematol. 1995. PMID: 7535243

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