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Search for publications relevant for "CYTOGENETIC ABNORMALITIES"
CYTOGENETIC ABNORMALITIES
Publication
Class
Person
Publication
Programmes
publication
Precise determination of primary cytogenetic abnormalities provides added value for stratification of chronic lymphocytic leukemia patients
2019 |
Faculty of Medicine in Pilsen
publication
Our experience with the detection of cytogenetic abnormalities that may be important diagnostic aids in some chilhood solid tumors, especially in bone and soft tissue sarcomas
2004 |
Publication without faculty affiliation
publication
Cytogenetic abnormalities predict survival after allogeneic hematopoietic stem cell transplantation for pediatric acute myeloid leukemia: a PDWP/EBMT study
2024 |
Second Faculty of Medicine
publication
Prognostic significance of cytogenetic abnormalities in patients in chronic phase of chronic myeloid leukemia treated with imatinib
Publication without faculty affiliation
publication
Negative prognostic significance of two or more cytogenetic abnormalities in multiple myeloma patients treated with autologous stem cell transplantation
2010 |
First Faculty of Medicine
publication
A novel oncocytoid papillary renal cell carcinoma, type 2, with aberrant cytogenetic abnormalities: oncocytic papillary renal cell carcinoma?
2013 |
Faculty of Medicine in Pilsen
publication
Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents
2017 |
Second Faculty of Medicine
publication
Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome
2010 |
First Faculty of Medicine
publication
Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome
2010 |
Second Faculty of Medicine
publication
Allogeneic stem cell transplantation can improve outcome of AML patients without complete cytogenetic response after induction and consolidation treatment
2015 |
Faculty of Medicine in Pilsen
publication
The response of FLi1, EKLF, TP53 (p53), PU.1, MDM2 gene expression in 5q- syndrome to lenalidomide treatment
Publication without faculty affiliation
publication
Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98
2010 |
First Faculty of Medicine
publication
Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98
2010 |
Second Faculty of Medicine
publication
Persistent Overall Survival Benefit and No Increased Risk of Second Malignancies With Bortezomib-Melphalan-Prednisone Versus Melphalan-Prednisone in Patients With Previously Untreated Multiple Myeloma
2013 |
First Faculty of Medicine
publication
Morphological differentiation of severe aplastic anaemia from hypocellular refractory cytopenia of childhood: reproducibility of histopathological diagnostic criteria
2012 |
Second Faculty of Medicine
publication
Variants of chromosome 9 in the newborn population and their clinical significance
2012 |
First Faculty of Medicine
publication
A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome
2010 |
First Faculty of Medicine
publication
Incidence and clinical significance of chromosomal abnormalities of heterochromatin area of human chromosome 9
Publication without faculty affiliation
publication
A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients
2013 |
First Faculty of Medicine, Third Faculty of Medicine
publication
A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome
2010 |
Second Faculty of Medicine
publication
Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7
1999 |
Second Faculty of Medicine
publication
Thrombocytopenia at diagnosis as an important negative prognostic marker in isolated 5q-MDS (IPSS low and intermediate-1)
2012 |
Publication without faculty affiliation
publication
Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia?
2017 |
Second Faculty of Medicine
publication
Cytogenetic and array comparative genomic hybridization analysis of a series of hepatoblastomas
2009 |
Second Faculty of Medicine
publication
Cutaneous involvement in multiple myeloma: a multi-institutional retrospective study of 53 patients
2016 |
Faculty of Medicine in Hradec Králové
publication
Near-tetraploid T-cell acute lymphoblastic leukaemia in childhood: Results of the AIEOP-BFM ALL studies
2022 |
Second Faculty of Medicine
publication
PH negative myeloproliferative neoplasms in Czech haematological centres - MIND analysis
2021 |
Faculty of Medicine in Hradec Králové
publication
Chromosomal 1q21 abnormalities in multiple myeloma: a review of translational, clinical research, and therapeutic strategies
2021 |
First Faculty of Medicine
publication
Incidence, diagnosis and treatment of myelodysplastic syndrome in children in the Czech Republic: results of the prospective study of the EWOG-MDS 1998-2002
2003 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Differential expression of homologous recombination DNA repair genes in the early and advanced stages of myelodysplastic syndrome
2017 |
First Faculty of Medicine, Second Faculty of Medicine