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gene cause
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Ing. Kateřina Mužíková
External person at Second Faculty of Medicine
36 publications
Publications
publication
BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations
2015 |
Second Faculty of Medicine
publication
The predictive strength of next-generation sequencing MRD detection for relapse compared with current methods in childhood ALL
2015 |
Second Faculty of Medicine
publication
Acute Leukemias with ETV6/ABL1 (TEL/ABL) Fusion: Poor Prognosis and Prenatal Origin
2010 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Prevalence of HHV-6 Integrated Chromosomally Among Children Treated for Acute Lymphoblastic or Myeloid Leukemia in the Czech Republic
2009 |
Second Faculty of Medicine
publication
Covert Preleukemia Driven by MLL Gene Fusion
2009 |
Second Faculty of Medicine
publication
Quantification of fusion transcript reveals a subgroup with distinct biological properties and predicts relapse in BCR/ABL-positive ALL: implications for residual disease monitoring
2009 |
Second Faculty of Medicine
publication
Detectable minimal residual disease before allogeneic hematopoietic stem cell transplantation predicts extremely poor prognosis in children with acute lymphoblastic leukemia
2007 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Childhood secondary ALL after ALL treatment
2007 |
Second Faculty of Medicine, Central Library of Charles University
publication
Prenatal origin of childhood AML occurs less frequently than in childhood ALL
2006 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Is WT1 gene hyperexpression a malignant cells marker?
2006 |
Second Faculty of Medicine
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