E. Drewke

Shear-induced unfolding triggers adhesion of von Willebrand factor fibers

Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS13 inhibitor: in vitro inhibition of ADAMTS13 activity by hemoglobin

Biological functions of fucose in mammals

The Clinical Sequelae of Intravascular Hemolysis and Extracellular Plasma Hemoglobin

Bleeding from gastrointestinal angioectasias is not related to bleeding disorders - a case control study

SWI/SNF nucleosome remodellers and cancer

Management of inherited von Willebrand disease in 2007

Elevated levels of von Willebrand Factor in cirrhosis support platelet adhesion despite reduced functional capacity

What is Intervertebral Disc Degeneration, and What Causes It?

The European guideline on management of major bleeding and coagulopathy following trauma: fourth edition

Clinical diagnosis of von Willebrand disease

Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome

Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies

Small RNAs are modified with N-glycans and displayed on the surface of living cells

Cleavage of ultra‐large von Willebrand factor by ADAMTS‐13 under flow conditions

von Willebrand disease (VWD): evidence‐based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA) ¹

Rituximab for chronic recurring thrombotic thrombocytopenic purpura: a case report and review of the literature

Measurement of von Willebrand factor-cleaving protease (ADAMTS-13) activity in plasma: a multicenter comparison of different assay methods

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

BIOCHEMISTRY AND GENETICS OF VON WILLEBRAND FACTOR

Impact, Diagnosis and Treatment of von Willebrand Disease

The inner of the two Muc2 mucin-dependent mucus layers in colon is devoid of bacteria

The ADAMTS metalloproteinases

Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura

Guidelines for the management of hemophilia

Laboratory Diagnosis of Congenital von Willebrand Disease

Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis

Von Willebrand factor multimers in virus-inactivated plasmas and F VIII concentrates.

Results of a Screening for von Willebrand Disease Type 2N in Patients with Suspected Haemophilia A or von Willebrand Disease Type 1

von Willebrand factor cleaving protease and ADAMTS13mutations in childhood TTP

Von Willebrand Disease Type 2M “Vicenza” in Italian and German Patients: Identification of the First Candidate Mutation (G3864A; R1205H) in 8 Families