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Voniatis, Dia

About me

Name: Dia

Surname: Voniatis

Academic title: Immunologist

Which is your area of expertise for the "Disease/group of diseases"?

  • Prevention and genetic counseling
  • Diagnostics

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Population screening for Thalassaemia, Diagnosis


Rare anemia Hemoglobinopathy Hemoglobin E disease Hemoglobin D disease Unstable hemoglobin disease Alpha-thalassemia and related diseases Alpha-thalassemia Hemoglobin H disease Hb Bart's hydrops fetalis Alpha-thalassemia-related diseases Alpha-thalassemia-X-linked intellectual disability syndrome Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Alpha-thalassemia-myelodysplastic syndrome Beta-thalassemia and related diseases Beta-thalassemia Beta-thalassemia major Beta-thalassemia intermedia Dominant beta-thalassemia Beta-thalassemia associated with another hemoglobin anomaly Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Delta-beta-thalassemia Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin Lepore-beta-thalassemia syndrome Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Sickle cell disease and related diseases Sickle cell anemia Sickle cell disease associated with an other hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hemoglobinopathy Toms River Hereditary methemoglobinemia Hemoglobin C disease Hemoglobin M disease Acquired methemoglobinemia Rare hemolytic anemia Rare constitutional hemolytic anemia Rare constitutional hemolytic anemia due to a red cell membrane anomaly Hereditary spherocytosis Hereditary elliptocytosis Distal renal tubular acidosis with anemia Hereditary stomatocytosis Overhydrated hereditary stomatocytosis Dehydrated hereditary stomatocytosis Rh deficiency syndrome Familial pseudohyperkalemia Southeast Asian ovalocytosis Hereditary cryohydrocytosis with reduced stomatin Hereditary cryohydrocytosis with normal stomatin Constitutional hemolytic anemia due to acanthocytosis Abetalipoproteinemia McLeod neuroacanthocytosis syndrome Primary CD59 deficiency

Which is your patient age coverage?

  • Pediatrics
  • Adults

Subnetwork representative:

  • Red blood cell defects

Member Go to member

Name english: Archbishop Makarios III Hospital

Name original: Νοσοκομείο Αρχιεπισκόπου Μακαρίου ΙΙΙ

Healthcare provider Go to healthcare provider

Name english: Archbishop Makarios III Hospital

Name original: Νοσοκομείο Αρχιεπισκόπου Μακαρίου ΙΙΙ


English name Original name Subnetworks of expertise Healthcare provider