Publications by authors named "Varvara Douna"

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Bone mineral status at diagnosis οf children with hematologic malignancy.
Maria Nikita, Artemis Doulgeraki, Margarita Baka, Charalampos Tsentidis, George Polyzois, Varvara Douna

Pediatr Hematol Oncol· May 2025

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Plasma Folate, Vitamin B12 and Homocysteine Levels in Children with Solid Tumors at Diagnosis; Results from a Pediatric Referral Centre.
Despoina N Maritsi, George Vartzelis, Helen Dana, Helen Kosmidis, Varvara Douna

Indian J Pediatr· May 2016

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Detection of acquired hemoglobinopathy in children with hematological malignancies at disease onset: results form a national referral centre.
Despoina N Maritsi, Helen V Kosmidis, Varvara Douna, Joanne Traeger-Synodinos, Maria N Tsolia

Int J Hematol· November 2013

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Acute megakaryoblastic leukemia with increased hematogones in children.
Marieta Anton-Harisi, Varvara Douna, Margarita Baka, Marina Servitzoglou, Helen V Kosmidis

J Pediatr Hematol Oncol· November 2012

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Variable and often severe phenotypic expression in patients with the α-thalassemic variant Hb Agrinio [α29(B10)Leu→Pro (α2)].
Joanne Traeger-Synodinos, Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Vasilis Ladis

Hemoglobin· March 2011

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Severe Eosinophilia in an infant with congenital acute myeloid leukemia with t(3;4;6)(q26;q25;q21): a case report.
Marieta Harisi, Varvara Douna, Margarita Baka, Marina Servitzoglou, Helen Kosmidi

J Pediatr Hematol Oncol· August 2010

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Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek family.
Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis

Hemoglobin· February 2009

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A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases.
Varvara Douna, Ioannis Papassotiriou, Anastasia Garoufi, Eleni Georgouli, Vassilis Ladis

Hemoglobin· September 2008

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First observation of Hb Taybe [Codons 38/39 (-Acc) Thr-->0 (alpha1)] in Greece: clinical and hematological findings in patients with co-inherited alpha+-thalassemia mutations.
Varvara Douna, Dimitra Liapi, Dimitrios Kampourakis, Zoe Repapinou, Ioannis Papassotiriou

Hemoglobin· September 2008

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Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutations.
Varvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Dimitra Liapi

Hemoglobin· September 2008

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