Age, beta thalassaemia trait, and iron-deficient anaemia significantly affect reticulocyte indices in pre-school children.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Works by STAMOULAKATOU, ALEXANDRA
Results: 22
1
2
A Novel Immunological Assay for Hepcidin Quantification in Human Serum.
- Published in:
- PLoS ONE, 2009, v. 4, n. 2, p. 1, doi. 10.1371/journal.pone.0004581
- By:
- Publication type:
- Article
3
Hb Souli, a 6 bp In-Frame Deletion on the HBA2 Gene ( HBA2: c.[41-46delCCTGGG]) Leads to α-Thalassemia Intermedia, When in Trans to a Single α-Globin Gene Deletion.
- Published in:
- Hemoglobin, 2015, v. 39, n. 1, p. 55, doi. 10.3109/03630269.2014.981827
- By:
- Publication type:
- Article
4
Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)].
- Published in:
- Hemoglobin, 2010, v. 34, n. 5, p. 430, doi. 10.3109/03630269.2010.509224
- By:
- Publication type:
- Article
5
Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp<sup>→</sup>Tyr (α2)] and Hb Agrinio [α29(B10)Leu<sup>→</sup>Pro (α2)] in a Greek Family
- Published in:
- Hemoglobin, 2008, v. 32, n. 6, p. 592, doi. 10.1080/03630260802507964
- By:
- Publication type:
- Article
6
A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly<sup>→</sup>Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases.
- Published in:
- Hemoglobin, 2008, v. 32, n. 4, p. 361, doi. 10.1080/03630260802173890
- By:
- Publication type:
- Article
7
First Observation of Hb Taybe [Codons 38/39 (-Acc) Thr<sup>→</sup>0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations.
- Published in:
- Hemoglobin, 2008, v. 32, n. 4, p. 371, doi. 10.1080/03630260802173973
- By:
- Publication type:
- Article
8
Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (-CCC); Pro<sup>→</sup>0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations.
- Published in:
- Hemoglobin, 2008, v. 32, n. 4, p. 379, doi. 10.1080/03630260802174021
- By:
- Publication type:
- Article
9
Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, G G C→G A C] Co-Inherited With a β + -Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family.
- Published in:
- Hemoglobin, 2006, v. 30, n. 4, p. 409, doi. 10.1080/03630260600867842
- By:
- Publication type:
- Article
10
Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE.
- Published in:
- Hemoglobin, 2001, v. 25, n. 1, p. 45, doi. 10.1081/HEM-100103069
- By:
- Publication type:
- Article
11
Is Ceftriaxone-Induced Biliary Pseudolithiasis Influenced by UDP-Glucuronosyltransferase 1A1 Gene Polymorphisms?
- Published in:
- 2011
- By:
- Publication type:
- Case Study
12
Deferiprone as an oral iron chelator in sickle cell disease.
- Published in:
- 2005
- By:
- Publication type:
- journal article
13
Ineffective erythropoiesis underlies the clinical heterogeneity of congenital dyserythropoietic anemia type II (CDA II).
- Published in:
- Pediatrics International, 2004, v. 46, n. 3, p. 274, doi. 10.1111/j.1442-200x.2004.01892.x
- By:
- Publication type:
- Article
14
A novel α<sup>0</sup>-thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.
- Published in:
- European Journal of Haematology, 2012, v. 88, n. 4, p. 356, doi. 10.1111/j.1600-0609.2012.01748.x
- By:
- Publication type:
- Article
15
Hydroxyurea Therapy in Thalassemia<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 120, doi. 10.1111/j.1749-6632.1998.tb10469.x
- By:
- Publication type:
- Article
16
Tissue Oxygenation in Patients with Hemoglobinopathy H.
- Published in:
- Pediatric Hematology & Oncology, 1997, v. 14, n. 4, p. 323, doi. 10.3109/08880019709041592
- By:
- Publication type:
- Article
17
Magnetic resonance imaging in the evaluation of iron overload in patients with beta thalassaemia and sickle cell disease.
- Published in:
- British Journal of Haematology, 2004, v. 126, n. 5, p. 736, doi. 10.1111/j.1365-2141.2004.05104.x
- By:
- Publication type:
- Article
18
Assessment of a new immunocytochemical technique in HbF-cell counting by a novel objective evaluation method.
- Published in:
- British Journal of Haematology, 2003, v. 123, n. 5, p. 948, doi. 10.1046/j.1365-2141.2003.04717.x
- By:
- Publication type:
- Article
19
Unusual phenotypic observations associated with a rare HbH disease genotype (--Med/α TSaudiα): implications for clinical management.
- Published in:
- British Journal of Haematology, 2002, v. 119, n. 1, p. 265, doi. 10.1046/j.1365-2141.2002.03777.x
- By:
- Publication type:
- Article
20
Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 3, p. 915, doi. 10.1046/j.1365-2141.2000.02448.x
- By:
- Publication type:
- Article
21
Modulating the oxygen affinity of human fetal haemoglobin with synthetic allosteric modulators.
- Published in:
- British Journal of Haematology, 1998, v. 102, n. 5, p. 1165, doi. 10.1046/j.1365-2141.1998.00886.x
- By:
- Publication type:
- Article
22
Hb Arta [β45 (CD4) Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β-thalassaemia.
- Published in:
- British Journal of Haematology, 1995, v. 91, n. 3, p. 595, doi. 10.1111/j.1365-2141.1995.tb05353.x
- By:
- Publication type:
- Article