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- Journal Article
- A1
- open access
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
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- Journal Article
- A1
- open access
Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome
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Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents
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- Journal Article
- A1
- open access
Bone marrow immunophenotyping by flow cytometry in refractory cytopenia of childhood
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Juvenile myelomonocytic leukemia : five genes, how many subtypes?
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Bone marrow immunophenotyping by flow cytometry in refractory cytopenia of childhood
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RASA4 undergoes DNA hypermethylation in resistant juvenile myelomonocytic leukemia
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Comparison of horse and rabbit antithymocyte globulin in immunosuppressive therapy for refractory cytopenia of childhood
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Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML
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Therapy-related myelodysplastic syndrome following treatment for childhood acute lymphoblastic leukemia: outcome of patients registered in the EWOG-MDS 98/06 studies
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IER3 expression in childhood myelodysplastic syndrome
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Aberrant DNA methylation characterizes juvenile myelomonocytic leukemia with poor outcome
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Mutations of the spliceosome complex genes occur in adult patients but are very rare in children with myeloid neoplasia
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Bresolin_2010_Gene exGene expression-based classification as an independent predictor of clinical outcome in juvenile myelomonocytic leukemia
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Refractory Cytopenia in Childhood (RCC) with normal karyotype is unlikely to progress to advanced MDS under a watch and wait strategy