Marcus Fager Ferrari

Clinical Coagulation, Malmö

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2024
Mark Sicklecellsjukdom - vanliga och farliga komplikationer
Björkman, Hedvig ; Fager Ferrari, Marcus ^LU ; Arvanitakis, Alexandros ^LU and Kjellander, Christian (2024) In Läkartidningen 121.
- Contribution to journal › Article
2021
Mark Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE
Smolag Klosowska, Karolina ^LU ; Fager Ferrari, Marcus ^LU ; Zetterberg, Eva ^LU ; Leinoe, Eva ; Ek, Torben ; Blom, Anna ^LU ; Rossing, Maria and Martin, Myriam ^LU (2021) In Frontiers in Immunology 12.
- Contribution to journal › Article
Mark Evaluation of the Sialidase Inhibitor Oseltamivir in GNE-associated Thrombocytopenia
Fager Ferrari, Marcus ^LU ; Smolag Klosowska, Karolina ^LU ; Zetterberg, Eva ^LU ; Leinoe, Eva ; Blom, A.M. ; Ek, Torben ; Rossing, Maria and Martin, Myriam ^LU (2021) The XXIX Congress of the International Society on Thrombosis and Haemostasis (ISTH) In Research and practice in thrombosis and haemostasis 5(S2). p.644-645
- Contribution to journal › Published meeting abstract
Mark Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen‐related genes
Fager Ferrari, Marcus ^LU ; Zetterberg, Eva ^LU ; Rossing, Maria ; Manon‐jensen, Tina ; Pehrsson, Martin ; Karsdal, Morten A. ; Lykkesfeldt, Jens and Leinoe, Eva (2021) In Haemophilia 27(1). p.69-77
- Contribution to journal › Article
Mark A rare case of IgE kappa monoclonal gammopathy of undetermined significance identified in a Swedish female
Fager Ferrari, Marcus ^LU ; Lemonakis, Konstantinos ^LU and Förnvik Jonsson, Magnus ^LU (2021) In Scandinavian Journal of Clinical and Laboratory Investigation 81(5). p.385-388
- Contribution to journal › Article
Mark Genetic Screening in Patients Suspected of Inherited Bleeding Disorders
Fager Ferrari, Marcus ^LU (2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
2020
Mark A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family
Fager Ferrari, Marcus ^LU ; Leinoe, Eva ; Rossing, Maria ; Norström, Eva ^LU and Zetterberg, Eva ^LU (2020) In Blood Coagulation and Fibrinolysis 31(7). p.481-484
- Contribution to journal › Article
Mark Collagen Turnover and Plasma Ascorbic Acid Levels in Patients Suspected of Inherited Bleeding Disorders Harboring Variants in Collagen-related Genes
Fager Ferrari, Marcus ^LU ; Zetterberg, Eva ^LU ; Rossing, Maria ; Manon-Jensen, Tina ; Pehrsson, Martin ; Karsdal, Morten ; Lykkesfeldt, Jens and Leinoe, Eva (2020) The XXVIII Congress of the International Society on Thrombosis and Haemostasis (ISTH) In Research and practice in thrombosis and haemostasis 4(S1). p.599-599
- Contribution to journal › Published meeting abstract
Mark Genetic screening of children with suspected inherited bleeding disorders
Andersson, Nadine ^LU ; Rossing, Maria ; Fager Ferrari, Marcus ^LU ; Gabrielaite, Migle ; Leinøe, Eva ; Ljung, Rolf ^LU ; Mårtensson, Annika ^LU ; Norström, Eva ^LU and Zetterberg, Eva ^LU (2020) In Haemophilia 26(2). p.314-324
- Contribution to journal › Article
2019
Mark A Heterozygous FGB Variant Causing Hypofibrinogenemia in a Swedish Family
Fager Ferrari, Marcus ^LU ; Leinoe, Eva ; Rossing, Maria and Zetterberg, Eva ^LU (2019) The XXVII Congress of the International Society on Thrombosis and Haemostasis (ISTH) In Research and practice in thrombosis and haemostasis 3(S1). p.367-369
- Contribution to journal › Published meeting abstract

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