about
Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.Asparagine synthetase (ASNS) gene polymorphism is associated with the outcome of childhood acute lymphoblastic leukemia by affecting early response to treatment.Usefulness of Post-Transplant Hematopoietic Chimera Monitoring by Use of the Quantitative Fluorescence Polymerase Chain Reaction Method.Heterozygous carriers of germline c.657_661del5 founder mutation in NBN gene are at risk of central nervous system relapse of B-cell precursor acute lymphoblastic leukemia.Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease.Biallelic loss of CDKN2A is associated with poor response to treatment in pediatric acute lymphoblastic leukemia.Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population.Fluorescence in situ hybridization BCR/ABL fusion signal rate in interphase nuclei of healthy volunteer donors: a test study for establishing false positive rateThe effectiveness of high-resolution-comparative genomic hybridization in detecting the most common chromosomal abnormalities in pediatric myelodysplastic syndromesStructural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemiaPolymorphism in IKZF1 gene affects age at onset of childhood acute lymphoblastic leukemiaClinical characteristics and analysis of treatment result in children with Ph-positive acute lymphoblastic leukaemia in Poland between 2005 and 2017Infection profile in children and adolescents with bone marrow failures treated with allogeneic hematopoietic stem cell transplantationThe importance of FDG PET/CT in the diagnostic process of the middle aortic syndrome in a 15-year-old boy patient with suspected systemic vasculitis and final diagnosis of Williams-Beuren syndromeImpact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantationComprehensive chromosomal aberrations in a case of a patient with TCF3-HLF-positive BCP-ALL
P50
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P50
description
researcher ORCID ID = 0000-0002-8760-0775
@en
wetenschapper
@nl
name
Monika Lejman
@ast
Monika Lejman
@en
Monika Lejman
@es
Monika Lejman
@nl
type
label
Monika Lejman
@ast
Monika Lejman
@en
Monika Lejman
@es
Monika Lejman
@nl
prefLabel
Monika Lejman
@ast
Monika Lejman
@en
Monika Lejman
@es
Monika Lejman
@nl
P106
P1153
16304074800
P21
P31
P496
0000-0002-8760-0775