Showing results (71-80 of 118) with videos related to

Sort By:
Pageof 12
Haematologica|October 14, 2011
A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesisSilvia Vettore, Fabiana Tezza, Alessandro Malara, et al.
Recenti Progressi in Medicina|May 7, 2002
[Chronic pain in the elderly]Mauro Zanocchi, Teresa Aimar, Roberta Risso, et al.
Simulation in Healthcare : Journal of the Society for Simulation in Healthcare|January 11, 2021
Life-Saving Procedures Performed While Wearing CBRNe Personal Protective Equipment: A Mannequin Randomized TrialGiulia Mormando, Matteo Paganini, Chiara Alexopoulos, et al.
Blood|July 20, 2006
Pediatric patients with essential thrombocythemia are mostly polyclonal and V617FJAK2 negativeMaria Luigia Randi, Maria Caterina Putti, Margherita Scapin, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 21, 2024
A β-Glucosyl Sterol Probe for in situ Fluorescent Labelling in Neuronal Cells to Investigate Neurodegenerative DiseasesGiuseppe Borsato, Francesco Carnio, Sara Lunardon, et al.
Blood|December 8, 2009
Src tyrosine kinase preactivation is associated with platelet hypersensitivity in essential thrombocythemia and polycythemia veraMaria Luigia Randi, Anna Maria Brunati, Margherita Scapin, et al.
European Journal of Haematology|January 28, 2014
Defective ADAMTS13 synthesis as a possible consequence of NASH in an obese patient with recurrent thrombotic thrombocytopenic purpuraAnna Maria Lombardi, Roberto Fabris, Giulia Berti de Marinis, et al.
Journal of Thrombosis and Thrombolysis|July 6, 2016
Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patientsGiulia Berti de Marinis, Stefano Novello, Silvia Ferrari, et al.
Cytometry. Part B, Clinical Cytometry|January 5, 2017
Activated Platelet-Derived and Leukocyte-Derived Circulating Microparticles and the Risk of Thrombosis in Heparin-Induced Thrombocytopenia: A Role for PF4-Bearing Microparticles?Elena Campello, Claudia M Radu, Elena Duner, et al.
European Journal of Medical Genetics|July 7, 2010
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defectSilvia Vettore, Daniela De Rocco, Bernhard Gerber, et al.
Pageof 12