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Diagnosis of respiratory syncytial virus and influenza A and B with cobas® Liat® from nasopharyngeal aspirations in pediatrics

Diagnostic microbiology and infectious disease, 2021-06, Vol.100 (2), p.115326-115326, Article 115326

2021

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Different profile of thrombin generation in children with acute lymphoblastic leukaemia treated with native or pegylated asparaginase: A cohort study

Pediatric blood & cancer, 2017-02, Vol.64 (2), p.294-301

2017

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Imaging of Juvenile Idiopathic Arthritis

The Radiologic clinics of North America, 2017-09, Vol.55 (5), p.1071

2017

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Serum calprotectin (S100A8/A9): a promising biomarker in diagnosis and follow-up in different subgroups of juvenile idiopathic arthritis

Rheumatic & musculoskeletal diseases open, 2021-06, Vol.7 (2), p.e001646

2021

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A pilot study of manual chronic partial exchange transfusion in children with sickle disease

Hematology (Luxembourg), 2015-06, Vol.20 (5), p.284-288

2015

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Evaluation of the procoagulant activity of endogenous phospholipids in the platelet-free plasma of children with sickle cell disease using functional assays

Thrombosis research, 2012-08, Vol.130 (2), p.259-264

2012

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Osteoid Osteoma: A Unique Presentation in a Child’s Lesser Toe

Case reports in orthopedics, 2021-01, Vol.2021, p.1-4

2021

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Patient preferences for gene therapy in haemophilia: Results from the PAVING threshold technique survey

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-11, Vol.27 (6), p.957-966

2021

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Is There Any Improvement of the Coagulation Imbalance in Sickle Cell Disease after Hematopoietic Stem Cell Transplantation?

Journal of clinical medicine, 2019-10, Vol.8 (11), p.1796

2019

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Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment

Pediatric blood & cancer, 2015-11, Vol.62 (11), p.1956-1961

2015

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Is Pica under-reported in children with sickle cell disease? A pilot study in a Belgian cohort

Hematology (Luxembourg), 2015-08, Vol.20 (7), p.429-432

2015

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Neonatal Screening for Sickle Cell Disease in Belgium for More than 20 Years: An Experience for Comprehensive Care Improvement

International journal of neonatal screening, 2018-12, Vol.4 (4), p.37-37

2018

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Automated RBC exchange compared to manual exchange transfusion for children with sickle cell disease is cost‐effective and reduces iron overload

Transfusion (Philadelphia, Pa.), 2018-06, Vol.58 (6), p.1356-1362

2018

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Use of hydroxyurea in prevention of stroke in children with sickle cell disease

Blood, 2008-01, Vol.111 (2), p.963-964

2008

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Thrombin generation reveals high procoagulant potential in the plasma of sickle cell disease children

American journal of hematology, 2012-02, Vol.87 (2), p.145-149

2012

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GCMB Mutation in Familial Isolated Hypoparathyroidism with Residual Secretion of Parathyroid Hormone

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.2487-2492

2005

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Reduction of the six-minute walk distance in children with sickle cell disease is correlated with silent infarct: results from a cross-sectional evaluation in a single center in Belgium

PloS one, 2014-10, Vol.9 (9), p.e108922-e108922

2014

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Efficacy and safety in patients with haemophilia A switching to octocog alfa (BAY 81–8973): Final results of the global real‐world study, TAURUS

European journal of haematology, 2023-01, Vol.110 (1), p.77-87

2023

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Effect of N‐acetylcysteine on pain in daily life in patients with sickle cell disease: a randomised clinical trial

British journal of haematology, 2018-08, Vol.182 (3), p.444-448

2018

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National Clinical Data Base for Sickle Cell Disease In Belgium

Blood, 2010-11, Vol.116 (21), p.2659-2659

2010

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Antibody deficiency due to a missense mutation in CD19 demonstrates the importance of the conserved tryptophan 41 in immunoglobulin superfamily domain formation

Human molecular genetics, 2011-05, Vol.20 (9), p.1854-1863

2011

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Transfusion support of autoimmune hemolytic anemia: how could the blood group genotyping help?

Translational research : the journal of laboratory and clinical medicine, 2014, Vol.163 (1), p.36-42

2014

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Neonatal screening improves sickle cell disease clinical outcome in Belgium

Journal of medical screening, 2018-06, Vol.25 (2), p.57-63

2018

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Etanercept improves linear growth and bone mass acquisition in MTX-resistant polyarticular-course juvenile idiopathic arthritis

Rheumatology (Oxford, England), 2010-08, Vol.49 (8), p.1550-1558

2010

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Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: the Belgian experience

Blood, 2005-04, Vol.105 (7), p.2685-2690

2005

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Diagnosis of respiratory syncytial virus and influenza A and B with cobas® Liat® from nasopharyngeal aspirations in pediatrics

Different profile of thrombin generation in children with acute lymphoblastic leukaemia treated with native or pegylated asparaginase: A cohort study

Imaging of Juvenile Idiopathic Arthritis

Serum calprotectin (S100A8/A9): a promising biomarker in diagnosis and follow-up in different subgroups of juvenile idiopathic arthritis

A pilot study of manual chronic partial exchange transfusion in children with sickle disease

Evaluation of the procoagulant activity of endogenous phospholipids in the platelet-free plasma of children with sickle cell disease using functional assays

Osteoid Osteoma: A Unique Presentation in a Child’s Lesser Toe

Patient preferences for gene therapy in haemophilia: Results from the PAVING threshold technique survey

Is There Any Improvement of the Coagulation Imbalance in Sickle Cell Disease after Hematopoietic Stem Cell Transplantation?

Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment

Is Pica under-reported in children with sickle cell disease? A pilot study in a Belgian cohort

Neonatal Screening for Sickle Cell Disease in Belgium for More than 20 Years: An Experience for Comprehensive Care Improvement

Automated RBC exchange compared to manual exchange transfusion for children with sickle cell disease is cost‐effective and reduces iron overload

Use of hydroxyurea in prevention of stroke in children with sickle cell disease

Thrombin generation reveals high procoagulant potential in the plasma of sickle cell disease children

GCMB Mutation in Familial Isolated Hypoparathyroidism with Residual Secretion of Parathyroid Hormone

Reduction of the six-minute walk distance in children with sickle cell disease is correlated with silent infarct: results from a cross-sectional evaluation in a single center in Belgium

Efficacy and safety in patients with haemophilia A switching to octocog alfa (BAY 81–8973): Final results of the global real‐world study, TAURUS

Effect of N‐acetylcysteine on pain in daily life in patients with sickle cell disease: a randomised clinical trial

National Clinical Data Base for Sickle Cell Disease In Belgium

Antibody deficiency due to a missense mutation in CD19 demonstrates the importance of the conserved tryptophan 41 in immunoglobulin superfamily domain formation

Transfusion support of autoimmune hemolytic anemia: how could the blood group genotyping help?

Neonatal screening improves sickle cell disease clinical outcome in Belgium

Etanercept improves linear growth and bone mass acquisition in MTX-resistant polyarticular-course juvenile idiopathic arthritis

Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: the Belgian experience

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