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Biological Chemistry
|
July 20, 2011
Characterization of human septin interactions
Kirstin Sandrock, Ingrid Bartsch, Susanne Bläser, et al.
Journal of Atherosclerosis and Thrombosis
|
September 5, 2014
Early diagnosis of acquired von Willebrand Syndrome (AVWS) is elementary for clinical practice in patients treated with ECMO therapy
Johannes Kalbhenn, Rene Schmidt, Lea Nakamura, et al.
BMC Pediatrics
|
August 14, 2022
Emicizumab in children: bleeding episodes and outcome before and after transition to Emicizumab
Hannah Glonnegger, Felicia Andresen, Friedrich Kapp, et al.
Diseases (Basel, Switzerland)
|
July 26, 2024
Catheter Intervention in a Patient with Intracranial Aneurysms and Glanzmann Thrombasthenia Caused by a Novel Homozygous Likely Pathogenic Variant in the <i>ITGA2B</i> Gene
Doris Boeckelmann, Lara von Dobeneck, Hans Henkes, et al.
Cells
|
January 8, 2023
Pervasive Platelet Secretion Defects in Patients with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
Johannes Kalbhenn, Jan-Steffen Pooth, Georg Trummer, et al.
Journal of Child Neurology
|
January 27, 2009
Unilateral venous thalamic infarction in a child mimicking a thalamic tumor
Verena Haug, Michaela Linder-Lucht, Barbara Zieger, et al.
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-III
Roman Crazzolara, Kathrin Maurer, Harald Schulze, 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 disease
André Jakob, Eva Schachinger, Simon Klau, et al.
Hamostaseologie
|
November 10, 2022
Laboratory Findings, Medical Imaging, and Clinical Outcome in Children with Cerebral Sinus Venous Thrombosis
Hannah Glonnegger, Nicole Glatthaar, Matthias Eckenweiler, et al.
Cells
|
October 23, 2021
A Novel Likely Pathogenic Variant in the <i>BLOC1S5</i> Gene Associated with Hermansky-Pudlak Syndrome Type 11 and an Overview of Human BLOC-1 Deficiencies
Doris Boeckelmann, Mira Wolter, Barbara Käsmann-Kellner, et al.
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of 15
Search research articles
Search
Showing results (41-50 of 147) with videos related to
Sort By:
Page
of 15
Biological Chemistry
|
July 20, 2011
Characterization of human septin interactions
Kirstin Sandrock, Ingrid Bartsch, Susanne Bläser, et al.
Journal of Atherosclerosis and Thrombosis
|
September 5, 2014
Early diagnosis of acquired von Willebrand Syndrome (AVWS) is elementary for clinical practice in patients treated with ECMO therapy
Johannes Kalbhenn, Rene Schmidt, Lea Nakamura, et al.
BMC Pediatrics
|
August 14, 2022
Emicizumab in children: bleeding episodes and outcome before and after transition to Emicizumab
Hannah Glonnegger, Felicia Andresen, Friedrich Kapp, et al.
Diseases (Basel, Switzerland)
|
July 26, 2024
Catheter Intervention in a Patient with Intracranial Aneurysms and Glanzmann Thrombasthenia Caused by a Novel Homozygous Likely Pathogenic Variant in the <i>ITGA2B</i> Gene
Doris Boeckelmann, Lara von Dobeneck, Hans Henkes, et al.
Cells
|
January 8, 2023
Pervasive Platelet Secretion Defects in Patients with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
Johannes Kalbhenn, Jan-Steffen Pooth, Georg Trummer, et al.
Journal of Child Neurology
|
January 27, 2009
Unilateral venous thalamic infarction in a child mimicking a thalamic tumor
Verena Haug, Michaela Linder-Lucht, Barbara Zieger, et al.
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-III
Roman Crazzolara, Kathrin Maurer, Harald Schulze, 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 disease
André Jakob, Eva Schachinger, Simon Klau, et al.
Hamostaseologie
|
November 10, 2022
Laboratory Findings, Medical Imaging, and Clinical Outcome in Children with Cerebral Sinus Venous Thrombosis
Hannah Glonnegger, Nicole Glatthaar, Matthias Eckenweiler, et al.
Cells
|
October 23, 2021
A Novel Likely Pathogenic Variant in the <i>BLOC1S5</i> Gene Associated with Hermansky-Pudlak Syndrome Type 11 and an Overview of Human BLOC-1 Deficiencies
Doris Boeckelmann, Mira Wolter, Barbara Käsmann-Kellner, et al.
Page
of 15