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Pediatric Blood & Cancer|April 10, 2015
A new mutation in the KINDLIN-3 gene ablates integrin-dependent leukocyte, platelet, and osteoclast function in a patient with leukocyte adhesion deficiency-IIIRoman Crazzolara, Kathrin Maurer, Harald Schulze, et al.
Transfusion|August 10, 2020
Naturally occurring point mutation Cys460Trp located in the I-EGF1 domain of integrin β3 alters the binding of some anti-HPA-1a antibodiesSarah Theresa Holzwarth, Behnaz Bayat, Jieqing Zhu, et al.
European Journal of Pediatrics|November 25, 2019
Von Willebrand factor parameters as potential biomarkers for disease activity and coronary artery lesion in patients with Kawasaki diseaseAndré Jakob, Eva Schachinger, Simon Klau, et al.
Hamostaseologie|November 10, 2022
Laboratory Findings, Medical Imaging, and Clinical Outcome in Children with Cerebral Sinus Venous ThrombosisHannah Glonnegger, Nicole Glatthaar, Matthias Eckenweiler, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 13, 2007
Septin expression in proliferative retinal membranesXiaorong Xin, Mona Pache, Barbara Zieger, et al.
Hamostaseologie|October 15, 2025
Understanding Congenital FXI Deficiency: Genetic Diagnosis and Correlation of Variant Detection Rate to Factor XI ActivityBehnaz Pezeshkpoor, Atanas Banchev, Barbara Preisler, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|December 29, 2014
Platelet dysfunction and acquired von Willebrand syndrome in patients with left ventricular assist devicesMaral Baghai, Claudia Heilmann, Friedhelm Beyersdorf, et al.
Hamostaseologie|January 13, 2022
Successful Secondary Endovascular Intervention in Pediatric Patients with Venous Thromboembolic EventsHannah Glonnegger, Barbara Zieger, Jochen Grohmann, et al.
Cells|August 26, 2022
Neonatal Platelets: Lower G12/13 Expression Contributes to Reduced Secretion of Dense GranulesAxel Schlagenhauf, Sheila Bohler, Mirjam Kunze, et al.
Gene|August 12, 2003
Isolation of new splice isoforms, characterization and expression analysis of the human septin SEPT8 (KIAA0202)Susanne Bläser, Katrin Jersch, Ina Hainmann, et al.
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