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Search for publications relevant for "genetic abnormalities"
genetic abnormalities
Publication
Class
Person
Publication
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publication
Genetic abnormalities in children with acute lymphoblastic leukaemia
1998 |
Second Faculty of Medicine
publication
Cyto- and molecular genetic abnormality differences between children < 2 years and older with acute myeloid leukemia
Publication without faculty affiliation
publication
Non-random genetic abnormalities in recurrent oligodendrocytic tumours: the utility of I-FISH
Publication without faculty affiliation
publication
Angiogenic cytokines in Bcell chronic lymphocytic leukemia : association with IGVH mutation status and genetic abnormalities
Publication without faculty affiliation
publication
Angiogenic activators in B-cell chronic lymphocytic leukemia: association with IgVH mutation status and genetic abnormalities
Publication without faculty affiliation
publication
Differences in cyto- and molecular genetic abnormalities between children under 2 years and older children with acute myeloid leukemia
Publication without faculty affiliation
publication
Detection of prognostically relevant genetic abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: recommendations from the Biology and Diagnosis Committee of the International Berlin-Frankfurt-Munster study group
2010 |
Second Faculty of Medicine
publication
Prognostic value of rare IKZF1 deletion in childhood B-cell precursor acute lymphoblastic leukemia: an international collaborative study
2016 |
Second Faculty of Medicine
publication
Biochemical methods used in amniotic fluid
2001 |
Second Faculty of Medicine, Central Library of Charles University
publication
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study
2008 |
First Faculty of Medicine
publication
Role of cytogenetic analysis in current management of childhood acute lymphoblastic leukemia treatment [Postavení cytogenetického vyšetrení v soucasném managementu lécby detské akutní lymfoblastické leukemie]
2015 |
Faculty of Medicine in Pilsen
publication
Extraordinary response to erlotinib therapy in a patient with lung adenocarcinoma exhibiting KRAS mutation and EGFR amplification
2011 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Anaesthetic management of patients with Williams syndrome
2018 |
First Faculty of Medicine
publication
Covert Preleukemia Driven by MLL Gene Fusion
2009 |
First Faculty of Medicine
publication
Trisomy X syndrome with dystonia and a pathogenic SATB1 variant
2021 |
First Faculty of Medicine
publication
Placental mesenchymal dysplasia - morphology and differential diagnosis
2021 |
Faculty of Medicine in Pilsen
publication
Lethal syndromes in pediatrics – three cases of trisomy 18
2023 |
Publication without faculty affiliation
publication
PHF6 mutations in paediatric acute myeloid leukaemia
2016 |
Second Faculty of Medicine
publication
Long-term remission of therapy-related acute myeloid leukemia with a new t(11;18)(q23;q21.2) translocation and KMT2A-ME2 (MLL-ME2) fusion gene
2015 |
Second Faculty of Medicine
publication
Advancements in the treatment of adult acute lymphoblastic leukaemia
2015 |
Publication without faculty affiliation
publication
Challenges in Diagnosing Myelodysplastic Syndromes in the Era of Genetic Testing: Proceedings of the 13th Workshop of the European Bone Marrow Working Group
2019 |
Faculty of Medicine in Pilsen
publication
What is your diagnosis? Answer: Spindle cell rhabdomyosarcoma
2017 |
Faculty of Medicine in Pilsen
publication
NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern
2013 |
Second Faculty of Medicine
publication
Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia?
2017 |
Second Faculty of Medicine
publication
Pustular psoriasis and related pustular skin diseases
2018 |
Faculty of Medicine in Pilsen
publication
Some remarks to the molecular genetic of colorectal cancer
2000 |
Second Faculty of Medicine
publication
New biological and genetic classification and therapeutically relevant categories in childhood B-cell precursor acute lymphoblastic leukemia
2018 |
Second Faculty of Medicine
publication
Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival
2012 |
Second Faculty of Medicine
publication
Is chronic plaque psoriasis triggered by microbiota in the skin?
2013 |
Faculty of Medicine in Pilsen
publication
Relationships between some genetic polymorphisms and clinical features of Alzheimer's disease
2015 |
First Faculty of Medicine