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You searched for: Author/Creator Cermak, Jaroslav

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1. Characterization of chromosome 11 breakpoints and the areas of deletion and amplification in patients with newly diagnosed acute myeloid leukemia. Issue 7 (12th April 2013)

2. Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes. (March 2016)

3. Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution. Issue 7 (25th March 2020)

4. Decitabine improves response rate and prolongs progression‐free survival in older patients with newly diagnosed acute myeloid leukemia and with monosomal karyotype: A subgroup analysis of the DACO‐016 trial. Issue 5 (24th February 2018)

5. Differential expression of homologous recombination DNA repair genes in the early and advanced stages of myelodysplastic syndrome. (24th July 2017)

6. Differing clinical features between Japanese and Caucasian patients with myelodysplastic syndromes: Analysis from the International Working Group for Prognosis of MDS. (October 2018)

7. Genome‐wide miRNA profiling in myelodysplastic syndrome with del(5q) treated with lenalidomide. (11th November 2014)

8. High level of full‐length cereblon mRNA in lower risk myelodysplastic syndrome with isolated 5q deletion is implicated in the efficacy of lenalidomide. (31st October 2014)

9. Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios. (18th February 2014)

10. Molecular Characterization of β-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations. (3rd May 2016)