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Risk of reactivated toxoplasmosis in haematopoietic stem cell transplant recipients: a prospective cohort study in a setting withholding prophylaxis

Clinical microbiology and infection, 2022-05, Vol.28 (5), p.733.e1-733.e5

2022

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Cytomegalovirus glycoprotein B and N genotypes in pediatric recipients of the hematopoietic stem cell transplant

Virology (New York, N.Y.), 2020-09, Vol.548, p.168-173

2020

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Persistent Antigen A after Minor ABO-Incompatible Hematopoietic Stem Cell Transplantation in Children: Two Case Reports

Transfusion medicine and hemotherapy, 2024-05, p.1-5

2024

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Factors Associated With Cytomegalovirus Infection in Pediatric Allogeneic Hematopoietic Stem Cell Transplant Recipients: A Prospective Single-Center Study

Experimental and clinical transplantation, 2021-11, Vol.19 (11), p.1156-1162

2021

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Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis

Journal of bone and mineral research, 2003-10, Vol.18 (10), p.1740-1747

2003

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Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B-cell acute lymphoblastic leukemia: A case report

Oncology letters, 2020-04, Vol.19 (4), p.2957-2962

2020

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A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b)

Gene, 2015-06, Vol.563 (2), p.115-119

2015

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Independent role of interleukin interleukin-6 and interleukin-8 in the etiology of transfusion reactions to platelet concentrates in children

Vojnosanitetski pregled, 2018, Vol.75 (4), p.390-397

2018

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Mobilization and Harvesting of Peripheral Blood Stem Cells in Pediatric Patients With Solid Tumors

Therapeutic apheresis and dialysis, 2011-12, Vol.15 (6), p.579-586

2011

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First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

Molecular cytogenetics, 2016-09, Vol.9 (1), p.70-70, Article 70

2016

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Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience

Journal of clinical immunology, 2014-04, Vol.34 (3), p.304-308

2014

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BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients

Oncology letters, 2016-05, Vol.11 (5), p.3240-3246

2016

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Comet assay and cytogenetic findings in differential diagnosis of Fanconi anemia

Genetika (Beograd), 2019, Vol.51 (3), p.1113-1126

2019

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Fanconi Anemia Is Characterized by Delayed Repair Kinetics of DNA Double-Strand Breaks

The Tohoku Journal of Experimental Medicine, 2010, Vol.221(1), pp.69-76

2010

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Atypical Strain of Toxoplasma gondii Causing Fatal Reactivation after Hematopoietic Stem Cell Transplantion in a Patient with an Underlying Immunological Deficiency

Journal of Clinical Microbiology, 2013-08, Vol.51 (8), p.2686-2690

2013

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Vitamin D3 Stimulates Proliferation Capacity, Expression of Pluripotency Markers, and Osteogenesis of Human Bone Marrow Mesenchymal Stromal/Stem Cells, Partly through SIRT1 Signaling

Biomolecules (Basel, Switzerland), 2022-02, Vol.12 (2), p.323

2022

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Risk factors for thrombosis in Serbian children

Blood coagulation & fibrinolysis, 2014-01, Vol.25 (1), p.25-32

2014

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Genotyping Fanconi anemia patients from Serbia reveals three novel FANCD2 variants

Genetika (Beograd), 2017, Vol.49 (2), p.559-572

2017

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Chromosomal instability in patients with Fanconi anemia from Serbia

Vojnosanitetski pregled, 2014-04, Vol.71 (4), p.368-372

2014

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Subclinical hypothyroidism in children and adolescents after hematopoietic stem cells transplantation without irradiation

Vojnosanitetski pregled, 2014-12, Vol.71 (12), p.1123-1127

2014

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Breakage and dislocation of the Hickman catheter in pediatric patient

Srpski arhiv za celokupno lekarstvo, 2024, p.64-64

2024

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A Single-Cell Raman Spectroscopy Analysis of Bone Marrow Mesenchymal Stem/Stromal Cells to Identify Inter-Individual Diversity

International journal of molecular sciences, 2022-04, Vol.23 (9), p.4915

2022

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Assessment of single nucleotide polymorphisms in screening 52 DNA repair and cell cycle control genes in Fanconi anemia patients

Genetika (Beograd), 2015, Vol.47 (2), p.695-710

2015

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Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia

Indian journal of pediatrics, 2014-03, Vol.81 (3), p.260-265

2014

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Influence of applied CD34+ cell dose on the survival of Hodgkin's lymphoma and multiple myeloma patients following autologous stem cell transplants

Vojnosanitetski pregled, 2020, Vol.77 (8), p.844-851

2020

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Risk of reactivated toxoplasmosis in haematopoietic stem cell transplant recipients: a prospective cohort study in a setting withholding prophylaxis

Cytomegalovirus glycoprotein B and N genotypes in pediatric recipients of the hematopoietic stem cell transplant

Persistent Antigen A after Minor ABO-Incompatible Hematopoietic Stem Cell Transplantation in Children: Two Case Reports

Factors Associated With Cytomegalovirus Infection in Pediatric Allogeneic Hematopoietic Stem Cell Transplant Recipients: A Prospective Single-Center Study

Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis

Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B-cell acute lymphoblastic leukemia: A case report

A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b)

Independent role of interleukin interleukin-6 and interleukin-8 in the etiology of transfusion reactions to platelet concentrates in children

Mobilization and Harvesting of Peripheral Blood Stem Cells in Pediatric Patients With Solid Tumors

First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience

BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients

Comet assay and cytogenetic findings in differential diagnosis of Fanconi anemia

Fanconi Anemia Is Characterized by Delayed Repair Kinetics of DNA Double-Strand Breaks

Atypical Strain of Toxoplasma gondii Causing Fatal Reactivation after Hematopoietic Stem Cell Transplantion in a Patient with an Underlying Immunological Deficiency

Vitamin D3 Stimulates Proliferation Capacity, Expression of Pluripotency Markers, and Osteogenesis of Human Bone Marrow Mesenchymal Stromal/Stem Cells, Partly through SIRT1 Signaling

Risk factors for thrombosis in Serbian children

Genotyping Fanconi anemia patients from Serbia reveals three novel FANCD2 variants

Chromosomal instability in patients with Fanconi anemia from Serbia

Subclinical hypothyroidism in children and adolescents after hematopoietic stem cells transplantation without irradiation

Breakage and dislocation of the Hickman catheter in pediatric patient

A Single-Cell Raman Spectroscopy Analysis of Bone Marrow Mesenchymal Stem/Stromal Cells to Identify Inter-Individual Diversity

Assessment of single nucleotide polymorphisms in screening 52 DNA repair and cell cycle control genes in Fanconi anemia patients

Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia

Influence of applied CD34+ cell dose on the survival of Hodgkin's lymphoma and multiple myeloma patients following autologous stem cell transplants

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