Abstracts (HTML) List of Authors

Adelhardt, Tina

Evaluation of Individualized Physiotherapy in Pediatric Patients with Severe Bleeding Disorders

Adolf, Daniela

Dokumentationsqualität und Therapieadhärenz: Daten der Haemoassist-Community

Aebi-Huber, Isabella

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at Enrolment until 2017

Akhter, Mohammad Suhail

Alpha-2 Macroglobulin: A Novel Putative Interacting Partner of FXIII/FXIIIB Subunit?

Albert, Thilo

AIM-Active-Studie – Hintergrund – Ziel – Design
LumiTope: Toward Improving the Performance of Identification of Antifactor VIII Antibodies in Congenital and Acquired Hemophilia A

Albisetti, Manuela

Erste Daten aus dem Schweizer Hämophilie-Register

Allerkamp, Hanna

Einfluss des Von-Willebrand-Faktors auf die porcine Angiogenese über das TIE-System

Al-Rifai, Rawya

Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell
Over Expression of Specific Transcription Factors to Boost FVIII Expression
Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model

Althaus, Karina

Combined Acquired Alpha- and Delta-Storage Pool Disease in Endstage Renal
Flow Cytometric Assessment of AKT Signaling in Platelet Activation: An Alternative Diagnostic Tool for Small Volumes of Blood
Apoptosis Inhibition: A Promising Approach for Cold Storage of Apheresis Platelet Concentrates
Autoantibody-Mediated Desialylation Impairs Human Thrombopoiesis and Platelet Life Span

Amling, Michael

Impact of Hepatitis C Infection on Bone Microstructure of Patients with Hemophilia

Anna, Pavlova

NGS for Diagnosing Inherited Bleeding, Thrombotic and Platelet Disorders: Points to Consider by Reporting Results—Primum Non Nocere, Secundum Cavere, Tertium Sanare
Diagnostic of Large Genetic Defects in Blood Coagulation Genes: NGS vs. MLPA

Ay, Cihan

Das Österreichische Hämophilie-Register