Search Results - "Varvara, Douna"

Infantile pyknocytosis: A rare cause of newborn hemolytic anemia two case reports by Evangelos, Christou, Konstantina, Avgerinou, Theodora, Bachou, Varvara, Douna, Mirsini, Mavrikou, Dimitris, Delis

“…Infantile pyknocytosis (IP) is a rare cause of neonatal hemolytic disease. The exact etiology of this entity remains unclear. It is characterized by prolonged…”
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Detection of acquired hemoglobinopathy in children with hematological malignancies at disease onset: results form a national referral centre by Maritsi, Despoina N., Kosmidis, Helen V., Douna, Varvara, Traeger-Synodinos, Joanne, Tsolia, Maria N., Kossiva, Lydia

“…Abnormal hemoglobin synthesis is usually inherited but may also arise as a secondary manifestation of a hematological neoplasia. The objective of this study is…”
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Plasma Folate, Vitamin B12 and Homocysteine Levels in Children with Solid Tumors at Diagnosis; Results from a Pediatric Referral Centre by Maritsi, Despoina N., Vartzelis, George, Dana, Helen, Kosmidis, Helen, Douna, Varvara, Kossiva, Lydia

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

“…We describe 2 patients, a 4-month-old male and a 17-month-old female, with de novo acute megakaryoblastic leukemia with increased number of hematogones at…”
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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 by Harisi, Marieta, Douna, Varvara, Baka, Margarita, Servitzoglou, Marina, Kosmidi, Helen, Anastasiou, Theodora

“…We report a case of acute myeloid leukemia with morphologic features of M7 according to the FAB (French-American-British) classification and severe…”
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Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)] by Traeger-Synodinos, Joanne, Douna, Varvara, Papassotiriou, Ioannis, Stamoulakatou, Alexandra, Ladis, Vasilis, Siahanidou, Tania, Fylaktou, Irine, Kanavakis, Emmanuel

“…Hb Agrinio [α29(B10)Leu→Pro] is a highly unstable variant, classified as a nondeletional α-thalassemia (α-thal) mutation. To date it has only been described in…”
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A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases by Douna, Varvara, Papassotiriou, Ioannis, Garoufi, Anastasia, Georgouli, Eleni, Ladis, Vassilis, Stamoulakatou, Alexandra, Metaxotou-Mavrommati, Anna, Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

“…Hb Adana is a highly unstable and rare α-globin hemoglobin (Hb) variant, to date described in only three families, in interaction with other α-thalassemia…”
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First Observation of Hb Taybe [Codons 38 39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations by Douna, Varvara, Liapi, Dimitra, Kampourakis, Dimitrios, Repapinou, Zoe, Papassotiriou, Ioannis, Stamoulakatou, Alexandra, Poziopoulos, Christos, Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

“…This report describes four unrelated Greek patients (one child and three adults) who all had an atypical thalassemia intermedia phenotype, characterized by…”
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Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro (α2)] in a Greek Family by Douna, Varvara, Papassotiriou, Ioannis, Stamoulakatou, Alexandra, Metaxotou-Mavrommati, Anna, Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

“…Hb Setif is a relatively rare, mildly unstable α2-globin hemoglobin (Hb) variant first described in an Algerian family, and subsequently in various populations…”
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Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36 37 (-CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations by Douna, Varvara, Papassotiriou, Ioannis, Metaxotou-Mavrommati, Anna, Stamoulakatou, Alexandra, Liapi, Dimitra, Kampourakis, Dimitrios, Tsilimigaki, Amalia, Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

“…We report four Greek cases (from three unrelated families), who all had a similar atypical thalassemia intermedia phenotype, characterized by chronic moderate…”
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