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The British Journal of Dermatology|July 28, 2012
The role of general practitioners in diagnosis of cutaneous melanoma: a population-based study in FranceF Grange, C Barbe, L Mas, et al.Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners|April 4, 2022
A simple extemporaneous oral suspension of aprepitant yields sufficient pharmacokinetic exposure in childrenA Laura Nijstad, Evelien de Vos-Kerkhof, Catherine F Enters-Weijnen, et al.Leukemia|May 16, 2015
NFATc1 as a therapeutic target in FLT3-ITD-positive AMLS K Metzelder, C Michel, M von Bonin, et al.European Psychiatry : the Journal of the Association of European Psychiatrists|March 5, 2015
EPA guidance on the early detection of clinical high risk states of psychosesF Schultze-Lutter, C Michel, S J Schmidt, et al.Blood|September 24, 2025
Fusion gene depletion eliminates stemness and induces bidirectional differentiation of acute myeloid leukemiaPolina K Derevyanko, Laura E Swart, L Daniel Mata Casimiro, et al.European Journal of Cancer (Oxford, England : 1990)|July 20, 2015
Prevention of central venous catheter-associated bloodstream infections in paediatric oncology patients using 70% ethanol locks: A randomised controlled multi-centre trialReineke A Schoot, C Heleen van Ommen, Theo Stijnen, et al.Journal of Neuro-Oncology|October 25, 2017
Correction to: A phase I/II study of gemcitabine during radiotherapy in children with newly diagnosed diffuse intrinsic pontine gliomaSophie E M Veldhuijzen van Zanten, Fatma E El-Khouly, Marc H A Jansen, et al.Journal of Clinical Immunology|June 28, 2022
Patients with Chromosome 11q Deletions Are Characterized by Inborn Errors of Immunity Involving both B and T LymphocytesElise J Huisman, A Rick Brooimans, Samone Mayer, et al.Cell|October 23, 2018
Modular Organization and Assembly of SWI/SNF Family Chromatin Remodeling ComplexesNazar Mashtalir, Andrew R D'Avino, Brittany C Michel, et al.Blood|November 10, 2021
Germline GATA1s-generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotypeHenrik Hasle, Ronald M Kline, Eigil Kjeldsen, et al.Pageof 134