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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 5-6
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Short Communication

Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition

Efthymia VlachakiAdult Thalassaemia Unit, 2nd Department of Internal Medicine, Aristotle University of Thessaloniki, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece;
,
Eleni GavriilakiHaematology Department, Bone Marrow Transplantation Unit, G. Papanicolaou Hospital, Thessaloniki, Greece; Correspondence[email protected]
,
Katerina KafantariAdult Thalassaemia Unit, 2nd Department of Internal Medicine, Aristotle University of Thessaloniki, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece;
,
Despoina AdamidouBlood Bank, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece;
,
Dimitris TsitsikasHaemoglobinopathy Service, Homerton University Hospital National Health Service Foundation Trust, London, UK;
,
Eleni ChasapopoulouBlood Bank, AHEPA Hospital, Thessaloniki, Greece
,
Achilles AnagnostopoulosHaematology Department, Bone Marrow Transplantation Unit, G. Papanicolaou Hospital, Thessaloniki, Greece;
&
Apostolos TsapasAdult Thalassaemia Unit, 2nd Department of Internal Medicine, Aristotle University of Thessaloniki, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece;
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Pages 339-341 | Received 22 Sep 2018, Accepted 20 Oct 2018, Published online: 09 Jan 2019

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