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Thrombosis and Haemostasis|March 11, 2010
Novel integrin-dependent platelet malfunction in siblings with leukocyte adhesion deficiency-III (LAD-III) caused by a point mutation in FERMT3Kerstin Jurk, Ansgar S Schulz, Beate E Kehrel, et al.The Lancet. Neurology|June 15, 2007
Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort studyGili Kenet, Fenella Kirkham, Thomas Niederstadt, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 12, 2022
Activated Platelets Upregulate β2 Integrin Mac-1 (CD11b/CD18) on Dendritic Cells, Which Mediates Heterotypic Cell-Cell InteractionHenry Nording, Manuela Sauter, Chaolan Lin, et al.Platelets|December 11, 2012
Novel mutation in Hermansky-Pudlak syndrome type 2 with mild immunological phenotypeKarin Kurnik, Ingrid Bartsch, Andrea Maul-Pavicic, et al.European Journal of Medical Genetics|November 6, 2012
MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlationsDaniela De Rocco, Barbara Zieger, Helen Platokouki, et al.Blood|March 23, 2006
Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type IIAnselm Enders, Barbara Zieger, Klaus Schwarz, et al.British Journal of Haematology|July 22, 2014
Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort studyVerena Limperger, Ulrich C Klostermeier, Gili Kenet, et al.Plos One|January 22, 2015
Functional comparison of induced pluripotent stem cell- and blood-derived GPIIbIIIa deficient plateletsMathias Orban, Alexander Goedel, Jessica Haas, et al.Thrombosis and Haemostasis|October 3, 2014
Role of protein S deficiency in children with venous thromboembolism. An observational international cohort studyUlrich C Klostermeier, Verena Limperger, Gili Kenet, et al.Thrombosis and Haemostasis|July 30, 2011
Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delayIngrid Bartsch, Kirstin Sandrock, Francois Lanza, et al.Pageof 14