Mariana M. Bonduel
B, Argentina
Last Updated: 09/26/2026
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Found 20 publications
Haemophilia B, severe childhood obesity and other extra-haematological features associated with similar 4Mb-deletions on Xq27: Clinical findings, molecular insights and literature update.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: September 16, 2022
Consensus-based clinical recommendations and research priorities for anticoagulant thromboprophylaxis in children hospitalized for COVID-19-related illness.
Journal: Journal of thrombosis and haemostasis : JTH
Published: July 11, 2020
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants.
Journal: Human mutation
Published: April 19, 2019
Official communication of the SSC: Recommendations for future research in catheter-related arterial thrombosis in children.
Journal: Research and practice in thrombosis and haemostasis
Published: September 28, 2018
Phenotypic and genotypic characterization of glucose-6-phosphate dehydrogenase deficiency in Argentina. Retrospective and descriptive study.
Journal: Archivos argentinos de pediatria
Published: September 05, 2018
American Society of Hematology 2018 Guidelines for management of venous thromboembolism: treatment of pediatric venous thromboembolism.
Journal: Blood advances
Published: August 19, 2018
Catheter-Related Arterial Thrombosis in Neonates and Children: A Systematic Review.
Journal: Thrombosis and haemostasis
Published: April 26, 2018
Rabbit antithymocyte globulin dose does not affect response or survival as first-line therapy for acquired aplastic anemia: a multicenter retrospective study.
Journal: Annals of hematology
Published: February 21, 2018
Repeat course of rabbit antithymocyte globulin as salvage following initial therapy with rabbit antithymocyte globulin in acquired aplastic anemia.
Journal: Haematologica
Published: April 12, 2015
Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series
Journal: Archivos argentinos de pediatria
Published: March 11, 2015
A new β(0) frameshift mutation, HBB: c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemia.
Journal: Hemoglobin
Published: October 01, 2014
Last Updated: 09/26/2026