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dr. M. Bartels

dr. M. Bartels

Assistant Professor - medical

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Research Output (36)

Untargeted metabolic profiling in dried blood spots identifies disease fingerprint for pyruvate kinase deficiency

Van Dooijeweert Birgit, Broeks Melissa H, Verhoeven-Duif Nanda M, Van Beers Eduard J, Nieuwenhuis Edward E S, Van Solinge Wouter W, Bartels Marije, Jans Judith J, Van Wijk Richard 10 Sep 2020, In: Haematologica. Online ahead of print , p. 1-20

Rivaroxaban compared with standard anticoagulants for the treatment of acute venous thromboembolism in children: a randomised, controlled, phase 3 trial

Male Christoph, Lensing Anthonie W. A., Palumbo Joseph S., Kumar Riten, Nurmeev Ildar, Hege Kerry, Bonnet Damien, Connor Philip, Hooimeijer Helene L., Torres Marcela, Chan Anthony K. C., Kenet Gili, Holzhauer Susanne, Santamaria Amparo, Amedro Pascal, Chalmers Elizabeth, Simioni Paolo, Bhat Rukhmi V., Yee Donald L., Lvova Olga, Beyer-Westendorf Jan, Biss Tina T., Martinelli Ida, Saracco Paola, Peters Marjolein, Kallay Krisztian, Gauger Cynthia A., Massicotte M. Patricia, Young Guy, Pap Akos F., Majumder Madhurima, Smith William T., Heubach Jurgen F., Berkowitz Scott D., Thelen Kirstin, Kubitza Dagmar, Crowther Mark, Prins Martin H., Monagle Paul, , Bartels M Jan 2020, In: Lancet haematology. 7 , p. E18-E27

Chapter 48: Erythrocyte Enzyme Disorders

Bartels M, van Beers Eduard, van Wijk Richard 2020, p. 749-784 35 p.

AML Subtype Is a Major Determinant of the Association between Prognostic Gene Expression Signatures and Their Clinical Significance

Wiggers Caroline R M, Baak Mirna L, Sonneveld Edwin, Nieuwenhuis Edward E S, Bartels Marije, Creyghton Menno P 10 Sep 2019, In: Cell Reports. 28 , p. 2866-2877.e5

Recognizing a Non-classical Telomeropathy before Hematopoietic Stem Cell Transplantation in Pediatric Patients:A Case Series

Nederlof Iris, Lindemans Caroline A, Bierings Marc B, Mohseny Alexander B, Bresters Dorine, Bartels Marije Aug 2019, In: HemaSphere. 3

The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis:A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis

van Vuren Annelies, van der Zwaag Bert, Huisjes Rick, Lak Nathalie, Bierings Marc, Gerritsen Egbert, van Beers Eduard, Bartels Marije, van Wijk Richard Aug 2019, In: HemaSphere. 3

Transcriptomic and Epigenomic Profiling of Histone Deacetylase Inhibitor Treatment Reveals Distinct Gene Regulation Profiles Leading to Impaired Neutrophil Development

Govers Anita M A P, Wiggers Caroline R M, van Boxtel Ruben, Mokry Michal, Nieuwenhuis Edward E S, Creyghton Menno P, Bartels Marije, Coffer Paul J Aug 2019, In: HemaSphere. 3

Red Blood Cells:Chasing Interactions

Pretini Virginia, Koenen Mischa H, Kaestner Lars, Fens Marcel H A M, Schiffelers Raymond M, Bartels Marije, Van Wijk Richard 31 Jul 2019, In: Frontiers in Physiology. 10

Characterization of the phenotype of human eosinophils and their progenitors in the bone marrow of healthy individuals

Hassani Marwan, van Staveren Selma, van Grinsven Erinke, Bartels Marije, Tesselaar Kiki, Leijte Guus, Kox Mathijs, Pickkers Peter, Vrisekoop Nienke, Koenderman Leo 17 May 2019, In: Haematologica. 105 , p. e52-e56 5 p.

Epigenetic drug screen identifies the histone deacetylase inhibitor NSC3852 as a potential novel drug for the treatment of pediatric acute myeloid leukemia

Wiggers Caroline R M, Govers Anita M A P, Lelieveld Daphne, Egan David A, Zwaan C Michel, Sonneveld Edwin, Coffer Paul J, Bartels Marije 1 May 2019, In: Pediatric Blood & Cancer. 66

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