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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 11, 2014
Successful management of a small infant with Kasabach-Merritt phenomenon using vincristine: a case reportMarina Economou, Andromachi Papagianni, Anastasia Tsigka, et al.
European Journal of Pediatrics|March 30, 2023
Therapeutic perspective for children and young adults living with thalassemia and sickle cell diseaseMarta Ferraresi, Daniele Lello Panzieri, Simona Leoni, et al.
International Journal of Molecular Sciences|December 16, 2017
Serum Levels of S100b and NSE Proteins in Patients with Non-Transfusion-Dependent Thalassemia as Biomarkers of Brain Ischemia and Cerebral VasculopathyAikaterini Kanavaki, Konstantinos Spengos, Maria Moraki, et al.
Biology|March 26, 2022
Heterozygosity of the Complex Corfu δ0β+ Thalassemic Allele (HBD Deletion and HBB:c.92+5G>A) RevisitedChristos Kattamis, Myrto Skafida, Polyxeni Delaporta, et al.
Leukemia Research|July 2, 2019
High resolution Chromosomal Microarray Analysis (CMA) enhances the genetic profile of pediatric B-cell Acute Lymphoblastic Leukemia patientsAnastasios Mitrakos, Antonis Kattamis, Katerina Katsibardi, et al.
Thrombosis and Haemostasis|September 28, 2006
Prevalence of thromboembolic events among 8,860 patients with thalassaemia major and intermedia in the Mediterranean area and IranAli Taher, Hussain Isma'eel, Ghassan Mehio, et al.
Blood Cells, Molecules & Diseases|January 30, 2010
Cystatin C levels in patients with beta-thalassemia during deferasirox treatmentIoannis Papassotiriou, Alexandra Margeli, Eugenia Hantzi, et al.
Pediatric Blood & Cancer|August 19, 2014
Clinical phenotype and genetic analysis of RPS19, RPL5, and RPL11 genes in Greek patients with Diamond Blackfan AnemiaPolyxeni Delaporta, Christalena Sofocleous, Eftichia Stiakaki, et al.
BMC Cardiovascular Disorders|February 10, 2021
Left ventricular deformation mechanics over time in patients with thalassemia major with and without iron overloadMichael J Bonios, Epameinontas Fountas, Polyxeni Delaporta, et al.
Haematologica|January 12, 2005
Sustained response to interferon alpha-2a in thalassemic patients with chronic hepatitis C. A prospective 8-year follow-up studyVassiliki Syriopoulou, George L Daikos, Stavroula L Kostaridou, et al.
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