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The Journal of clinical investigation, ISSN 1558-8238, 2018, Volume 128, Issue 9, pp. 4057 - 4073
Quantitative abnormalities of the von Willebrand factor-factor VIII (VWF-FVIII) complex associate with inherited bleeding or thrombotic disorders.... 
MEDICINE, RESEARCH & EXPERIMENTAL | VONWILLEBRAND-FACTOR | PLASMA-LEVELS | COAGULATION-FACTOR-VIII | HEMOPHILIA-A MICE | IN-VIVO | KUPFFER CELLS | LINKAGE ANALYSIS | HYALURONAN RECEPTOR | VON-WILLEBRAND-FACTOR | GENOME-WIDE ASSOCIATION | Factor VIII - immunology | von Willebrand Factor - immunology | Factor VIII - pharmacokinetics | Humans | Middle Aged | Child, Preschool | Half-Life | Infant | Male | Cell Adhesion Molecules, Neuronal - deficiency | Genetic Variation | Young Adult | Endocytosis | von Willebrand Factor - pharmacokinetics | Adult | Female | Cell Adhesion Molecules, Neuronal - metabolism | Protein Stability | Child | von Willebrand Factor - metabolism | Endothelial Cells - metabolism | Liver - metabolism | Mice, Inbred C57BL | Factor VIII - chemistry | Cell Adhesion Molecules, Neuronal - genetics | Mice, Knockout | Endothelial Cells - immunology | Animals | von Willebrand Factor - chemistry | Adolescent | Protein Binding | Aged | Liver - cytology | Mice | Factor VIII - metabolism | Drug Combinations | Cell receptors | Genetic aspects | Immune response | Health aspects | Von Willebrand factor | Endothelium | Antigens | Immunoglobulins | Disease | Immunoregulation | Liver | Immune clearance | Systematic review | Genomes | Kinases | Thrombosis | Endothelial cells | Studies | Coagulation factors | Phagocytes | Immunogenicity | Blood platelets | Hemophilia | Plasma levels | Mutation | Hyaluronic acid
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Haemophilia : the official journal of the World Federation of Hemophilia, ISSN 1351-8216, 2016, Volume 22, Issue 1, pp. 87 - 95
Journal Article