Lista de obras - Danuta Januszkiewicz-Lewandowska

A coding variant in NLRP1 is associated with autoimmune Addison's disease.

artículo científico publicado en 2010

A genome-wide association study on medulloblastoma

artículo científico publicado en 2020

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

scientific article published on 06 March 2019

Analysis of TLR2, TLR4, and TLR9 single nucleotide polymorphisms in children with bacterial meningitis and their healthy family members.

artículo científico publicado en 2017

Applications of the Grading Scales for the Detection of Ototoxicity in Children after Treatment of Neuroblastoma and Extracranial Germinal Tumor

artículo científico publicado en 2022

Assessment of the Usefulness of Multiplex Real-Time PCR Tests in the Diagnostic and Therapeutic Process of Pneumonia in Hospitalized Children: A Single-Center Experience

artículo científico publicado en 2017

Association of the CYP27B1 C(-1260)A polymorphism with autoimmune Addison's disease

artículo científico publicado en 2009

Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia.

artículo científico publicado en 2006

Bilateral Nephroblastoma with Dilated Cardiomyopathy as an Indication for Off-Protocol Treatment: A Case Report

artículo científico publicado en 2020

Distribution of HCV genotypes in Poland

artículo científico publicado en 2013

Distribution of polymorphisms rs12979860, rs8099917 and rs12980275 IL28B in patients with chronic hepatitis C.

artículo científico publicado en 2017

Does vaccination ensure protection? Assessing diphtheria and tetanus antibody levels in a population of healthy children: A cross-sectional study.

artículo científico publicado en 2016

Effect of immunomodulatory treatment of multiple sclerosis on lymphocyte surface immunomarkers.

artículo científico publicado en 2003

Effect of irradiation on DNA synthesis, NBN gene expression and chromosomal stability in cells with NBN mutations

scientific article published on 25 January 2017

Efficacy of idarubicin in the treatment of childhood acute non-lymphoblastic leukemia: report of Polish Pediatric Leukemia/Lymphoma Study Group

artículo científico publicado el 1 de enero de 2003

Env gene expression of human endogenous retrovirus-k and human endogenous retrovirus-w in childhood acute leukemia cells

artículo científico publicado en 2013

FKBP5 polymorphism is associated with insulin resistance in children and adolescents with obesity

artículo científico publicado en 2016

Functional variants of gene encoding folate metabolizing enzyme and methotrexate-related toxicity in children with acute lymphoblastic leukemia.

artículo científico publicado en 2015

GCK and HNF1alpha mutations and polymorphisms in Polish women with gestational diabetes.

artículo científico publicado en 2006

Genes and childhood leukemia.

artículo científico publicado en 2015

Genes and their single nucleotide polymorphism involved in innate immune response in central nervous system in bacterial meningitis: review of literature data.

artículo científico publicado en 2018

Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia

artículo científico publicado en 2013

HCMV infections after hematopoietic stem cell transplantation--diagnostic methods and importance of viral DNA level monitoring

artículo científico publicado en 2015

HCV Infection and Interferon-Based Treatment Induce p53 Gene Transcription in Chronic Hepatitis C Patients.

artículo científico publicado en 2015

Hepatitis G virus co-infection may affect the elimination of hepatitis C virus RNA from the peripheral blood of hemodialysis patients.

artículo científico publicado en 2001

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

artículo científico publicado en 2019

How many single-nucleotide polymorphisms (SNPs) must be tested in order to prove susceptibility to bacterial meningitis in children? Analysis of 11 SNPs in seven genes involved in the immune response and their effect on the susceptibility to bacteri

artículo científico publicado en 2018

I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer.

artículo científico publicado en 2007

Imatinib in the treatment of chronic myeloid leukemia in children and adolescents is effective and well tolerated: Report of the Polish Pediatric Study Group for the Treatment of Leukemias and Lymphomas.

artículo científico publicado en 2018

Interleukin 10 gene single nucleotide polymorphisms in Polish patients with chronic hepatitis C: Analysis of association with severity of disease and treatment outcome.

artículo científico publicado en 2016

Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis

artículo científico publicado en 2014

MSRV pol sequence copy number as a potential marker of multiple sclerosis

artículo científico publicado en 2003

Mutations in Pol gene of hepatitis B virus in patients with chronic hepatitis B before and after therapy with nucleoside/nucleotide analogues.

artículo científico publicado en 2014

No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.

artículo científico publicado en 2018

Outcome of refractory and relapsed acute myeloid leukemia in children treated during 2005-2011 - experience of the Polish Pediatric Leukemia/Lymphoma Study Group (PPLLSG).

artículo científico publicado en 2014

PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

artículo científico publicado en 2010

Paediatric hospitalisation numbers for influenza in 2016-2019 seasons underline importance of vaccination

artículo científico publicado en 2019

Pediatric Inflammatory Multisystem Syndrome (PIMS) Did Occur in Poland during Months with Low COVID-19 Prevalence, Preliminary Results of a Nationwide Register

scientific article published on 22 October 2020

Ph-negative isolated myeloid sarcoma with NPM1 gene mutation in adolescent with Ph-positive chronic myeloid leukemia in remission after treatment with allogeneic bone marrow transplantation and imatinib mesylate.

artículo científico publicado en 2015

Pneumocystis pneumonia in children - the relevance of chemoprophylaxis in different groups of immunocompromised and immunocompetent paediatric patients

artículo científico publicado en 2015

Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia.

artículo científico publicado en 2008

Polymorphisms in microRNA target sites modulate risk of lymphoblastic and myeloid leukemias and affect microRNA binding

artículo científico publicado en 2014

Polymorphisms of the Toll-Like Receptor-3 Gene in Autoimmune Adrenal Failure and Type 1 Diabetes in Polish Patients.

artículo científico publicado en 2015

Presence of hepatitis C virus (HCV)-RNA in peripheral blood mononuclear cells in HCV serum negative patients during interferon and ribavirin therapy.

artículo científico publicado en 2007

Prevalence of IFNL3 rs4803217 single nucleotide polymorphism and clinical course of chronic hepatitis C.

artículo científico publicado en 2017

Prevalence of the most frequent BRCA1 mutations in Polish population

artículo científico publicado en 2011

RAD50 gene mutations are not likely a risk factor for breast cancer in Poland.

artículo científico publicado en 2010

RNA-HCV viral load in serum, peripheral blood mononuclear cells and liver in children with chronic hepatitis C.

artículo científico publicado en 2012

Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in Humans

artículo científico publicado en 2019

Rhabdomyosarcoma in children - current pathologic and molecular classification

artículo científico publicado en 2018

Significance of molecular identification of hepatitis C virus RNA in diagnosis of cryptogenic hepatitis in children.

artículo científico publicado en 2001

Szczepienia u dzieci z chorobą nowotworową − aktualne polskie zalecenia

artículo científico publicado en 2017

The Profile of Microorganisms Responsible for Port-Related Bacteremia in Pediatric Hemato-Oncological Patients

artículo científico publicado en 2020

The methylenetetrahydrofolate reductase 677T-1298C haplotype is a risk factor for acute lymphoblastic leukemia in children

artículo científico publicado en 2017

The prevalence of mixed genotype infections in Polish patients with hepatitis C.

artículo científico publicado en 2015

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

artículo científico publicado en 2008

Thiopurine S-methyltransferase phenotype-genotype correlation in children with acute lymphoblastic leukemia.

artículo científico publicado en 2012

Too young to be vaccinated: hospitalizations caused by varicella among children in the first year of life.

artículo científico publicado en 2017

Transmission of HCV infection among long-term hospitalized onco-haematological patients.

artículo científico publicado en 2003

Treatment failure in children with acute myelocytic leukemia: over 25-year experience of Polish Pediatric Leukemia/Lymphoma Study Group with four consecutive unified treatment protocols for childhood acute myelocytic leukemia

artículo científico publicado el 1 de enero de 2010

Usefulness of inflammatory biomarkers in discriminating between bacterial and aseptic meningitis in hospitalized children from a population with low vaccination coverage.

artículo científico publicado en 2016

Utility of quantitative EBV DNA measurements in cerebrospinal fluid for diagnosis and monitoring of treatment of central nervous system EBV-associated post-transplant lymphoproliferative disorder after allogenic hematopoietic stem cell transplantati

artículo científico publicado en 2014

Vaccine-Derived Immunity in Children With Cancer-Analysis of Anti-Tetanus and Anti-Diphtheria Antibodies Changes after Completion of Antineoplastic Therapy.

artículo científico publicado en 2015

With a little help from a computer: discriminating between bacterial and viral meningitis based on dominance-based rough set approach analysis

artículo científico

[Cytogenetic analysis of secondary myelodysplastic syndrome after rhabdomysarcoma treatment--case report]

artículo científico publicado en 2012

[Epstein-Barr virus infection - life cycle, methods of diagnosis, associated diseases]

artículo científico publicado en 2011

[Genetic determination of smell]

artículo científico publicado en 2001

[Intermediate doses of cytosine arabinoside in the treatment of acute non-lymphoblastic leukaemia in children]

artículo científico publicado en 2000

[Prevalence of TT virus in patients with hepatitis B,C and hepatitis of unknown etiology]

artículo científico publicado en 2002

[Role of TT virus in pathogenesis of liver diseases--the prevalence of TTV in patients and healthy individuals]

artículo científico publicado en 2002

[TT virus--characteristics, occurrence and routes of transmission].

artículo científico publicado en 2002

[Treatment results of children with neuroblastoma: report of Polish Pediatric Solid Tumor Group]

artículo científico publicado en 2010

Lista de obras de Danuta Januszkiewicz-Lewandowska

A coding variant in NLRP1 is associated with autoimmune Addison's disease.

A genome-wide association study on medulloblastoma

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

Analysis of TLR2, TLR4, and TLR9 single nucleotide polymorphisms in children with bacterial meningitis and their healthy family members.

Applications of the Grading Scales for the Detection of Ototoxicity in Children after Treatment of Neuroblastoma and Extracranial Germinal Tumor

Assessment of the Usefulness of Multiplex Real-Time PCR Tests in the Diagnostic and Therapeutic Process of Pneumonia in Hospitalized Children: A Single-Center Experience

Association of the CYP27B1 C(-1260)A polymorphism with autoimmune Addison's disease

Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia.

Bilateral Nephroblastoma with Dilated Cardiomyopathy as an Indication for Off-Protocol Treatment: A Case Report

Distribution of HCV genotypes in Poland

Distribution of polymorphisms rs12979860, rs8099917 and rs12980275 IL28B in patients with chronic hepatitis C.

Does vaccination ensure protection? Assessing diphtheria and tetanus antibody levels in a population of healthy children: A cross-sectional study.

Effect of immunomodulatory treatment of multiple sclerosis on lymphocyte surface immunomarkers.

Effect of irradiation on DNA synthesis, NBN gene expression and chromosomal stability in cells with NBN mutations

Efficacy of idarubicin in the treatment of childhood acute non-lymphoblastic leukemia: report of Polish Pediatric Leukemia/Lymphoma Study Group

Env gene expression of human endogenous retrovirus-k and human endogenous retrovirus-w in childhood acute leukemia cells

FKBP5 polymorphism is associated with insulin resistance in children and adolescents with obesity

Functional variants of gene encoding folate metabolizing enzyme and methotrexate-related toxicity in children with acute lymphoblastic leukemia.

GCK and HNF1alpha mutations and polymorphisms in Polish women with gestational diabetes.

Genes and childhood leukemia.

Genes and their single nucleotide polymorphism involved in innate immune response in central nervous system in bacterial meningitis: review of literature data.

Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia

HCMV infections after hematopoietic stem cell transplantation--diagnostic methods and importance of viral DNA level monitoring

HCV Infection and Interferon-Based Treatment Induce p53 Gene Transcription in Chronic Hepatitis C Patients.

Hepatitis G virus co-infection may affect the elimination of hepatitis C virus RNA from the peripheral blood of hemodialysis patients.

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

How many single-nucleotide polymorphisms (SNPs) must be tested in order to prove susceptibility to bacterial meningitis in children? Analysis of 11 SNPs in seven genes involved in the immune response and their effect on the susceptibility to bacteri

I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer.

Imatinib in the treatment of chronic myeloid leukemia in children and adolescents is effective and well tolerated: Report of the Polish Pediatric Study Group for the Treatment of Leukemias and Lymphomas.

Interleukin 10 gene single nucleotide polymorphisms in Polish patients with chronic hepatitis C: Analysis of association with severity of disease and treatment outcome.

Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis

MSRV pol sequence copy number as a potential marker of multiple sclerosis

Mutations in Pol gene of hepatitis B virus in patients with chronic hepatitis B before and after therapy with nucleoside/nucleotide analogues.

No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.

Outcome of refractory and relapsed acute myeloid leukemia in children treated during 2005-2011 - experience of the Polish Pediatric Leukemia/Lymphoma Study Group (PPLLSG).

PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

Paediatric hospitalisation numbers for influenza in 2016-2019 seasons underline importance of vaccination

Pediatric Inflammatory Multisystem Syndrome (PIMS) Did Occur in Poland during Months with Low COVID-19 Prevalence, Preliminary Results of a Nationwide Register

Ph-negative isolated myeloid sarcoma with NPM1 gene mutation in adolescent with Ph-positive chronic myeloid leukemia in remission after treatment with allogeneic bone marrow transplantation and imatinib mesylate.

Pneumocystis pneumonia in children - the relevance of chemoprophylaxis in different groups of immunocompromised and immunocompetent paediatric patients

Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia.

Polymorphisms in microRNA target sites modulate risk of lymphoblastic and myeloid leukemias and affect microRNA binding

Polymorphisms of the Toll-Like Receptor-3 Gene in Autoimmune Adrenal Failure and Type 1 Diabetes in Polish Patients.

Presence of hepatitis C virus (HCV)-RNA in peripheral blood mononuclear cells in HCV serum negative patients during interferon and ribavirin therapy.

Prevalence of IFNL3 rs4803217 single nucleotide polymorphism and clinical course of chronic hepatitis C.

Prevalence of the most frequent BRCA1 mutations in Polish population

RAD50 gene mutations are not likely a risk factor for breast cancer in Poland.

RNA-HCV viral load in serum, peripheral blood mononuclear cells and liver in children with chronic hepatitis C.

Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in Humans

Rhabdomyosarcoma in children - current pathologic and molecular classification

Significance of molecular identification of hepatitis C virus RNA in diagnosis of cryptogenic hepatitis in children.

Szczepienia u dzieci z chorobą nowotworową − aktualne polskie zalecenia

The Profile of Microorganisms Responsible for Port-Related Bacteremia in Pediatric Hemato-Oncological Patients

The methylenetetrahydrofolate reductase 677T-1298C haplotype is a risk factor for acute lymphoblastic leukemia in children

The prevalence of mixed genotype infections in Polish patients with hepatitis C.

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

Thiopurine S-methyltransferase phenotype-genotype correlation in children with acute lymphoblastic leukemia.

Too young to be vaccinated: hospitalizations caused by varicella among children in the first year of life.

Transmission of HCV infection among long-term hospitalized onco-haematological patients.

Treatment failure in children with acute myelocytic leukemia: over 25-year experience of Polish Pediatric Leukemia/Lymphoma Study Group with four consecutive unified treatment protocols for childhood acute myelocytic leukemia

Usefulness of inflammatory biomarkers in discriminating between bacterial and aseptic meningitis in hospitalized children from a population with low vaccination coverage.

Utility of quantitative EBV DNA measurements in cerebrospinal fluid for diagnosis and monitoring of treatment of central nervous system EBV-associated post-transplant lymphoproliferative disorder after allogenic hematopoietic stem cell transplantati

Vaccine-Derived Immunity in Children With Cancer-Analysis of Anti-Tetanus and Anti-Diphtheria Antibodies Changes after Completion of Antineoplastic Therapy.

With a little help from a computer: discriminating between bacterial and viral meningitis based on dominance-based rough set approach analysis

[Cytogenetic analysis of secondary myelodysplastic syndrome after rhabdomysarcoma treatment--case report]

[Epstein-Barr virus infection - life cycle, methods of diagnosis, associated diseases]

[Genetic determination of smell]

[Intermediate doses of cytosine arabinoside in the treatment of acute non-lymphoblastic leukaemia in children]

[Prevalence of TT virus in patients with hepatitis B,C and hepatitis of unknown etiology]

[Role of TT virus in pathogenesis of liver diseases--the prevalence of TTV in patients and healthy individuals]

[TT virus--characteristics, occurrence and routes of transmission].

[Treatment results of children with neuroblastoma: report of Polish Pediatric Solid Tumor Group]