E. Leinoe

发表

Haemostatic function and biomarkers of endothelial damage before and after RBC transfusion in patients with haematologic disease

H. Birgens, S. Ostrowski, A. Larsen, 2015, Vox sanguinis.

Iron overload and iron chelating agent exposure in anemia-associated outer retinal degeneration: a case report and review of the literature

M. Larsen, E. Leinoe, B. K. Mortensen, 2021, BMC Ophthalmology.

A case of thrombocytopenia and multiple thromboses after vaccination with ChAdOx1 nCoV-19 against SARS-CoV-2

J. Goetze, A. Hvas, N. Kirkby, 2021, Blood Advances.

Clinical management, ethics and informed consent related to multi‐gene panel‐based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH

K. Downes, P. Noris, A. Greinacher, 2020, Journal of thrombosis and haemostasis : JTH.

Measuring the impact of a restrictive transfusion guideline in patients with acute myeloid leukaemia

H. Birgens, E. Leinoe, R. Hoeg, 2013, Vox sanguinis.

Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

William J. Astle, Sri V. V. Deevi, Matthew C. Sims, 2020, medRxiv.

Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen‐related genes

M. Karsdal, M. Rossing, J. Lykkesfeldt, 2020, Haemophilia : the official journal of the World Federation of Hemophilia.

A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family

M. Rossing, E. Norström, E. Leinoe, 2020, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

William J. Astle, Sri V. V. Deevi, Matthew C. Sims, 2020, medRxiv.

Multiple platelet defects identified by flow cytometry at diagnosis in acute myeloid leukaemia

H. Johnsen, E. Leinoe, E. Kjaersgaard, 2004, British journal of haematology.

GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis

W. Ouwehand, K. Downes, D. Trégouët, 2021, Journal of thrombosis and haemostasis : JTH.

Levels of procoagulant microparticles expressing phosphatidylserine contribute to bleeding phenotype in patients with inherited thrombocytopenia.

M. Rossing, S. Ostrowski, E. Leinoe, 2021, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.