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Co-Existence of Hereditary Pyrimidine 5'-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation.
Agapidou, A; Theodoridou, S; Tegos, K; Mandala, E; Leukou, E; Karakasidou, O; Aletra, B; Sevastidou, A; Alemayehou, M; Voskaridou, E.
Affiliation
  • Agapidou A; Hippokration Hospital of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece.
  • Theodoridou S; Laikon Hospital of Athens, Thalassemia Center, Athens, Greece.
  • Tegos K; NIMITS, Military Hospital, Athens, Greece.
  • Mandala E; Aristotelion University of Thessaloniki, 4th Unit of Internal Medicine, Thessaloniki, Greece.
  • Leukou E; Hippokration Hospital of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece.
  • Karakasidou O; Hippokration Hospital of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece.
  • Aletra B; Hippokration Hospital of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece.
  • Sevastidou A; Hippokration Hospital of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece.
  • Alemayehou M; Hippokration Hospital of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece.
  • Voskaridou E; Laikon Hospital of Athens, Thalassemia Center, Athens, Greece.
Turk J Haematol ; 29(4): 434-5, 2012 Dec.
Article in En | MEDLINE | ID: mdl-24385739
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Turk J Haematol Year: 2012 Document type: Article Affiliation country: Greece Country of publication: Turkey
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Turk J Haematol Year: 2012 Document type: Article Affiliation country: Greece Country of publication: Turkey