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Medical and Pediatric Oncology|October 12, 2002
On the origin of EEG-slowing and encephalopathy during induction treatment of acute lymphoblastic leukemiaRudolf Korinthenberg, Bernadette Scheuring, Joachim Boos, et al.
Orphanet Journal of Rare Diseases|October 17, 2022
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failureAyami Yoshimi, Kaori Ishikawa, Charlotte Niemeyer, et al.
Leukemia & Lymphoma|May 27, 2004
Marked thrombocytosis in a child with advanced myelodysplastic syndromeAlexander Claviez, Bona Ngoumou, Lana Harder, et al.
Frontiers in Pediatrics|November 28, 2022
Leukoreductive response to the combination of sorafenib and chemotherapy in hyperleukocytosis of FLT3-ITD mutated pediatric AMLFranziska Schmidt, Miriam Erlacher, Charlotte Niemeyer, et al.
The Cochrane Database of Systematic Reviews|August 6, 2010
Deferasirox for managing transfusional iron overload in people with sickle cell diseaseJoerg J Meerpohl, Gerd Antes, Gerta Rücker, et al.
European Journal of Pediatrics|May 13, 2004
Life-threatening complications of transient abnormal myelopoiesis in neonates with Down syndromeSabine Dormann, Marcus Krüger, Roland Hentschel, et al.
Pediatric Hematology and Oncology|August 22, 2007
Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parentsSevgi Yetgin, Selin Aytac, Serap Kalkanoglu, et al.
European Journal of Haematology|June 9, 2004
WT1 gene expression: useful marker for minimal residual disease in childhood myelodysplastic syndromes and juvenile myelo-monocytic leukemia?Peter Bader, Charlotte Niemeyer, Gerrit Weber, et al.
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