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fSCIG 10% in pediatric primary immunodeficiency diseases: a European post-authorization safety study

Allergy, asthma, and clinical immunology, 2024-09, Vol.20 (1), p.47-9, Article 47

2024

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Microchimaerismus kimutatása nagy érzékenységű droplet digitális PCR technikával és szerepe a vérképzőőssejt-transzplantált betegek monitorozásában

Orvosi hetilap, 2024-02, Vol.165 (8), p.297-308

2024

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Detection of microchimerism with high sensitivity droplet digital PCR technique and its significance in monitoring of hematopoietic stem cell transplanted patients

Orvosi hetilap, 2024-02, Vol.165 (8), p.297

2024

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The Impact of Qualification and Hospice Education on Staff Attitudes during Palliative Care in Pediatric Oncology Wards-A National Survey

Children (Basel), 2024-02, Vol.11 (2), p.178

2024

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Low rate of nonrelapse mortality in under-4-year-olds with ALL given chemotherapeutic conditioning for HSCT: a phase 3 FORUM study

Blood advances, 2024-01, Vol.8 (2), p.416-428

2024

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Similar Overall Survival and Event-Free Survival for Patients Under or over the Age of 14 Years, but More Chronic Graft Versus Host Disease and Non-Relapse Mortality in the “Older” Patients

Blood, 2023-11, Vol.142 (Supplement 1), p.3548-3548

2023

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Gaucher-kór és az ajánlott új diagnosztikai algoritmus

Hematológia-transzfuziológia : HT : a Magyar Hematológiai és Transzfuziológiai Társaság lapja, 2023-10, Vol.56 (2), p.76-80

2023

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Chromosomal breakage tests in the differential diagnosis of Fanconi anemia and aplastic anemia

European journal of haematology, 2023-08, Vol.111 (2), p.254-262

2023

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Next-Generation Sequencing–Based Genomic Profiling of Children with Acute Myeloid Leukemia

The Journal of molecular diagnostics : JMD, 2023-08, Vol.25 (8), p.555-568

2023

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Infekciók kockázatának csökkentése veleszületett és szerzett komplementdefektusokban: Irodalmi áttekintés és javaslat hazai gyakorlatra

Orvosi hetilap, 2023-06, Vol.164 (25), p.971-980

2023

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Reducing the risk of infections in hereditary and acquired complement deficiencies.

Orvosi hetilap, 2023-06, Vol.164 (25), p.971

2023

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Bone Turnover Marker for the Evaluation of Skeletal Remodelling in Autosomal Recessive Osteopetrosis after Haematopoietic Stem Cell Transplantation: A Case Report

Children (Basel, Switzerland), 2023, Vol.10 (4)

2023

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BT595, a 10% Human Normal Immunoglobulin, for Replacement Therapy of Primary Immunodeficiency Disease: Results of a Subcohort Analysis in Children

Journal of clinical immunology, 2023-04, Vol.43 (3), p.557-567

2023

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Empagliflozin restores neutropenia and neutrophil dysfunction in a young patient with severe congenital neutropenia type 4

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2023-01, Vol.11 (1), p.344-346.e1

2023

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Peripheral Bone Relapse of Paediatric TCF3-HLF Positive Acute Lymphoblastic Leukaemia during Haematopoietic Stem Cell Transplantation: A Case Report

Children (Basel, Switzerland), 2022, Vol.9 (12)

2022

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Superior Graft-Versus-Leukemia Effect in Matched Unrelated Donor Versus HLA-Identical Sibling Pediatric Recipients Transplanted for Acute Lymphoblastic Leukemia within the Forum Study

Blood, 2022-11, Vol.140 (Supplement 1), p.903-905

2022

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Relapse Is the Most Common Treatment Failure Post HSCT in Children with ALL below 4 Years of Age Given a Chemo-Based Conditioning Regimen. Results from the Prospective Multinational Forum-Trial

Blood, 2022-11, Vol.140 (Supplement 1), p.897-899

2022

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Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

Blood, 2022-10, Vol.140 (14), p.1635-1649

2022

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Efficacy, safety and pharmacokinetics of a new 10% normal human immunoglobulin for intravenous infusion, BT595, in children and adults with primary immunodeficiency disease

Vox sanguinis, 2022-10, Vol.117 (10), p.1153-1162

2022

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Case Report: A Child With Hemophilia A Serves as Donor for Hematopoietic Stem Cell Transplantation to Cure His Brother’s Severe Aplastic Anemia

Pathology oncology research, 2022-06, Vol.28

2022

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Correction to: Non-lupus full-house nephropathy—immune dysregulation as a rare cause of pediatric nephrotic syndrome: Answers

Pediatric nephrology (Berlin, West), 2022-06, Vol.37 (6), p.1429-1429

2022

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Non-lupus full-house nephropathy—immune dysregulation as a rare cause of pediatric nephrotic syndrome: Questions

Pediatric nephrology (Berlin, West), 2022-05, Vol.37 (5), p.1049-1051

2022

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fSCIG 10% in pediatric primary immunodeficiency diseases: a European post-authorization safety study

Microchimaerismus kimutatása nagy érzékenységű droplet digitális PCR technikával és szerepe a vérképzőőssejt-transzplantált betegek monitorozásában

Detection of microchimerism with high sensitivity droplet digital PCR technique and its significance in monitoring of hematopoietic stem cell transplanted patients

The Impact of Qualification and Hospice Education on Staff Attitudes during Palliative Care in Pediatric Oncology Wards-A National Survey

Low rate of nonrelapse mortality in under-4-year-olds with ALL given chemotherapeutic conditioning for HSCT: a phase 3 FORUM study

Similar Overall Survival and Event-Free Survival for Patients Under or over the Age of 14 Years, but More Chronic Graft Versus Host Disease and Non-Relapse Mortality in the “Older” Patients

Outcome of Children with B-Cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL) with Hypodiploidy or BCR-ABL1 Fusion Given Allogeneic Hematopoietic Stem Cell Transplantation (HSCT): Results from the Prospective Forum Study

Gaucher-kór és az ajánlott új diagnosztikai algoritmus

PersonALL: a genetic scoring guide for personalized risk assessment in pediatric B-cell precursor acute lymphoblastic leukemia

PB1699: GENOMIC AND TRANSCRIPTOMIC PROFILING REVEALS NOVEL GENE FUSIONS AND MARKERS OF CLINICAL RESPONSE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA

Chromosomal breakage tests in the differential diagnosis of Fanconi anemia and aplastic anemia

Next-Generation Sequencing–Based Genomic Profiling of Children with Acute Myeloid Leukemia

Infekciók kockázatának csökkentése veleszületett és szerzett komplementdefektusokban: Irodalmi áttekintés és javaslat hazai gyakorlatra

Reducing the risk of infections in hereditary and acquired complement deficiencies.

Bone Turnover Marker for the Evaluation of Skeletal Remodelling in Autosomal Recessive Osteopetrosis after Haematopoietic Stem Cell Transplantation: A Case Report

BT595, a 10% Human Normal Immunoglobulin, for Replacement Therapy of Primary Immunodeficiency Disease: Results of a Subcohort Analysis in Children

Empagliflozin restores neutropenia and neutrophil dysfunction in a young patient with severe congenital neutropenia type 4

Peripheral Bone Relapse of Paediatric TCF3-HLF Positive Acute Lymphoblastic Leukaemia during Haematopoietic Stem Cell Transplantation: A Case Report

Superior Graft-Versus-Leukemia Effect in Matched Unrelated Donor Versus HLA-Identical Sibling Pediatric Recipients Transplanted for Acute Lymphoblastic Leukemia within the Forum Study

Relapse Is the Most Common Treatment Failure Post HSCT in Children with ALL below 4 Years of Age Given a Chemo-Based Conditioning Regimen. Results from the Prospective Multinational Forum-Trial

Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

Efficacy, safety and pharmacokinetics of a new 10% normal human immunoglobulin for intravenous infusion, BT595, in children and adults with primary immunodeficiency disease

Case Report: A Child With Hemophilia A Serves as Donor for Hematopoietic Stem Cell Transplantation to Cure His Brother’s Severe Aplastic Anemia

Correction to: Non-lupus full-house nephropathy—immune dysregulation as a rare cause of pediatric nephrotic syndrome: Answers

Non-lupus full-house nephropathy—immune dysregulation as a rare cause of pediatric nephrotic syndrome: Questions

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