Publications in OpenAlex of which a co-author is affiliated to this organization
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| Title | DOI |
|---|---|
| https://doi.org/10.1093/nar/gkw955 | NOVOPlasty: de novo assembly of organelle genomes from whole genome data |
| https://doi.org/10.1017/s001216220500112x | Proposed definition and classification of cerebral palsy, April 2005 |
| https://doi.org/10.1016/j.resuscitation.2010.08.021 | European Resuscitation Council Guidelines for Resuscitation 2010 Section 1. Executive summary |
| https://doi.org/10.1056/nejmoa0805817 | Gene Therapy for Immunodeficiency Due to Adenosine Deaminase Deficiency |
| https://doi.org/10.1038/ng.2414 | Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature |
| https://doi.org/10.1053/j.gastro.2006.12.003 | Induction and Maintenance Infliximab Therapy for the Treatment of Moderate-to-Severe Crohn’s Disease in Children |
| https://doi.org/10.1038/ncb2521 | The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r |
| https://doi.org/10.1056/nejmoa1205099 | Two Randomized Trials of Canakinumab in Systemic Juvenile Idiopathic Arthritis |
| https://doi.org/10.1016/s0140-6736(07)61126-x | A treatment protocol for infants younger than 1 year with acute lymphoblastic leukaemia (Interfant-99): an observational study and a multicentre randomised trial |
| https://doi.org/10.1002/ajmg.a.36887 | Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 |
| https://doi.org/10.1093/brain/awx054 | Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders |
| https://doi.org/10.1093/annonc/mdp233 | Safety and efficacy of first-line bevacizumab with FOLFOX, XELOX, FOLFIRI and fluoropyrimidines in metastatic colorectal cancer: the BEAT study |
| https://doi.org/10.1182/blood-2016-10-745711 | Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation |
| https://doi.org/10.1097/mpg.0000000000001594 | Joint ESPGHAN/NASPGHAN Guidelines for the Management of Helicobacter pylori in Children and Adolescents (Update 2016) |
| https://doi.org/10.1016/j.pediatrneurol.2006.09.016 | Pathophysiology of Duchenne Muscular Dystrophy: Current Hypotheses |
| https://doi.org/10.3945/ajcn.113.064071 | Lower protein content in infant formula reduces BMI and obesity risk at school age: follow-up of a randomized trial |
| https://doi.org/10.1089/thy.2020.0333 | Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology |
| https://doi.org/10.1016/s1474-4422(13)70258-8 | Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study |
| https://doi.org/10.1182/blood.v99.8.2734 | Comparison of Escherichia coli-asparaginase with Erwinia-asparaginase in the treatment of childhood lymphoid malignancies: results of a randomized European Organisation for Research and Treatment of Cancer---Children's Leukemia Group phase 3 trial |
| https://doi.org/10.1056/nejmoa2009965 | Risdiplam in Type 1 Spinal Muscular Atrophy |
| https://doi.org/10.1056/nejmoa1314432 | Somatic Mutations in Cerebral Cortical Malformations |
| https://doi.org/10.1093/humrep/dev128 | Live birth after autograft of ovarian tissue cryopreserved during childhood: Figure 1 |
| https://doi.org/10.1038/5102 | Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome |
| https://doi.org/10.2337/diacare.24.11.1923 | Good Metabolic Control Is Associated With Better Quality of Life in 2,101 Adolescents With Type 1 Diabetes |
| https://doi.org/10.1038/s41564-024-01705-x | Personalized bacteriophage therapy outcomes for 100 consecutive cases: a multicentre, multinational, retrospective observational study |
| https://doi.org/10.1016/j.smrv.2010.01.002 | The emotional brain and sleep: An intimate relationship |
| https://doi.org/10.1016/j.nmd.2013.12.011 | Diagnostic approach to the congenital muscular dystrophies |
| https://doi.org/10.1016/j.resuscitation.2010.08.012 | European Resuscitation Council Guidelines for Resuscitation 2010 Section 6. Paediatric life support |
| https://doi.org/10.3201/eid1010.040241 | ArcobacterSpecies in Humans1 |
| https://doi.org/10.1111/dmcn.12922 | Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations |
| https://doi.org/10.1210/jc.2007-0354 | 11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations |
| https://doi.org/10.1038/sj.bmt.1701291 | Haematopoietic stem cell transplantation for sickle cell anaemia: the first 50 patients transplanted in Belgium |
| https://doi.org/10.1097/mpg.0b013e3182227e90 | Evidence‐based Guidelines From ESPGHAN and NASPGHAN for Helicobacter pylori Infection in Children |
| https://doi.org/10.1542/peds.84.3.542 | Sleep Problems in Healthy Preadolescents |
| https://doi.org/10.2337/diacare.24.8.1342 | Persistent Differences Among Centers Over 3 Years in Glycemic Control and Hypoglycemia in a Study of 3,805 Children and Adolescents With Type 1 Diabetes From the Hvidøre Study Group |
| https://doi.org/10.1016/s1474-4422(14)70195-4 | Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study |
| https://doi.org/10.1007/s00134-019-05922-5 | Nutritional support for children during critical illness: European Society of Pediatric and Neonatal Intensive Care (ESPNIC) metabolism, endocrine and nutrition section position statement and clinical recommendations |
| https://doi.org/10.1182/blood.v88.6.1960.bloodjournal8861960 | Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial |
| https://doi.org/10.1016/j.cgh.2011.11.026 | Induction and Maintenance Therapy With Infliximab for Children With Moderate to Severe Ulcerative Colitis |
| https://doi.org/10.1111/j.1398-9995.2004.00556.x | The prevalence of positive reactions in the atopy patch test with aeroallergens and food allergens in subjects with atopic eczema: a European multicenter study |
| https://doi.org/10.1016/j.ajhg.2009.04.016 | DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III |
| https://doi.org/10.1002/art.25057 | Long‐term efficacy of the interleukin‐1 receptor antagonist anakinra in ten patients with neonatal‐onset multisystem inflammatory disease/chronic infantile neurologic, cutaneous, articular syndrome |
| https://doi.org/10.1093/hmg/ddp435 | Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci |
| https://doi.org/10.1111/j.1469-7580.2010.01245.x | Early microglial colonization of the human forebrain and possible involvement in periventricular white‐matter injury of preterm infants |
| https://doi.org/10.1136/hrt.2002.007138 | Long term outcome up to 30 years after the Mustard or Senning operation: a nationwide multicentre study in Belgium |
| https://doi.org/10.1016/s1474-4422(21)00251-9 | Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial |
| https://doi.org/10.1164/rccm.201001-0137oc | Ataluren (PTC124) Induces Cystic Fibrosis Transmembrane Conductance Regulator Protein Expression and Activity in Children with Nonsense Mutation Cystic Fibrosis |
| https://doi.org/10.1016/j.ajhg.2009.10.012 | Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness |
| https://doi.org/10.1002/(sici)1096-9136(199809)15:9<752::aid-dia678>3.0.co;2-w | Insulin management and metabolic control of Type 1 diabetes mellitus in childhood and adolescence in 18 countries |
| https://doi.org/10.1038/ng.278 | Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness |
| https://doi.org/10.1016/s1470-2045(19)30617-5 | Vinorelbine and continuous low-dose cyclophosphamide as maintenance chemotherapy in patients with high-risk rhabdomyosarcoma (RMS 2005): a multicentre, open-label, randomised, phase 3 trial |
| https://doi.org/10.1136/gut.2006.091272 | Prospective multicentre study on antibiotic resistance of Helicobacter pylori strains obtained from children living in Europe |
| https://doi.org/10.1186/1750-1172-8-8 | Recommendations for the management of tyrosinaemia type 1 |
| https://doi.org/10.1016/j.jaci.2008.09.027 | Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: Inconsistent correlation between forkhead box protein 3 expression and disease severity |
| https://doi.org/10.2337/dc07-0475 | Continuing Stability of Center Differences in Pediatric Diabetes Care: Do Advances in Diabetes Treatment Improve Outcome? |
| https://doi.org/10.1093/bja/aen054 | Perioperative anaemia management: consensus statement on the role of intravenous iron |
| https://doi.org/10.1200/jco.19.00456 | Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
| https://doi.org/10.1093/ajcp/aqw076 | Performances of the H-Score for Diagnosis of Hemophagocytic Lymphohistiocytosis in Adult and Pediatric Patients |
| https://doi.org/10.1016/j.ejmg.2005.04.015 | Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification |
| https://doi.org/10.1177/0883073810381924 | Consensus Statement on Standard of Care for Congenital Muscular Dystrophies |
| https://doi.org/10.1210/jc.2010-1024 | Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients |
| https://doi.org/10.1016/j.gaitpost.2010.07.018 | Low vision affects dynamic stability of gait |
| https://doi.org/10.1016/s1474-4422(21)00367-7 | Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial |
| https://doi.org/10.1016/j.resuscitation.2010.08.014 | European Resuscitation Council Guidelines for Resuscitation 2010 Section 9. Principles of education in resuscitation |
| https://doi.org/10.1172/jci89626 | Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency |
| https://doi.org/10.1038/s41588-019-0417-8 | Atlas of group A streptococcal vaccine candidates compiled using large-scale comparative genomics |
| https://doi.org/10.1067/mob.2003.81 | Results of systematic screening for minor degrees of fetal renal pelvis dilatation in an unselected population |
| https://doi.org/10.1002/humu.21304 | Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectruma |
| https://doi.org/10.1016/j.ajhg.2011.04.018 | Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2 |
| https://doi.org/10.1111/j.1651-2227.2008.01152.x | Congenital heart disease in 111 225 births in Belgium: birth prevalence, treatment and survival in the 21st century |
| https://doi.org/10.1016/s1470-2045(09)70154-8 | Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH study |
| https://doi.org/10.1016/j.bja.2019.09.012 | 2019 EACTS/EACTA/EBCP guidelines on cardiopulmonary bypass in adult cardiac surgery |
| https://doi.org/10.1056/nejmoa2214171 | Blinatumomab Added to Chemotherapy in Infant Lymphoblastic Leukemia |
| https://doi.org/10.1016/j.pediatrneurol.2006.01.014 | Recognition of Emotional Facial Expressions in Attention-Deficit Hyperactivity Disorder |
| https://doi.org/10.1111/j.1432-1033.1992.tb19848.x | Structure and orientation of the surfactant‐associated protein C in a lipid bilayer |
| https://doi.org/10.1038/ng.749 | Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity |
| https://doi.org/10.1191/0961203304lu525oa | Autologous stem cell transplantation for systemic lupus erythematosus |
| https://doi.org/10.1016/s1470-2045(18)30337-1 | Addition of dose-intensified doxorubicin to standard chemotherapy for rhabdomyosarcoma (EpSSG RMS 2005): a multicentre, open-label, randomised controlled, phase 3 trial |
| https://doi.org/10.1111/j.1464-5491.2008.02399.x | Are family factors universally related to metabolic outcomes in adolescents with Type 1 diabetes? |
| https://doi.org/10.1093/brain/awn026 | REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31 |
| https://doi.org/10.1016/j.ajhg.2012.07.006 | A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia |
| https://doi.org/10.1037/0894-4105.21.6.778 | Response inhibition deficit is involved in poor decision making under risk in nonamnesic individuals with alcoholism. |
| https://doi.org/10.1111/j.1365-2141.2007.06592.x | Matched‐related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research |
| https://doi.org/10.1056/nejmoa2207418 | Expectant Management or Early Ibuprofen for Patent Ductus Arteriosus |
| https://doi.org/10.1002/mrdd.20093 | Sexual health care in persons with intellectual disabilities |
| https://doi.org/10.1007/s00213-006-0695-6 | Alcohol cues increase cognitive impulsivity in individuals with alcoholism |
| https://doi.org/10.1007/s00431-002-1037-2 | Insulin injection regimens and metabolic control in an international survey of adolescents with type 1 diabetes over 3 years: results from the Hvidore study group |
| https://doi.org/10.1016/j.tvjl.2005.04.024 | Epidemiology of dog bites: A Belgian experience of canine behaviour and public health concerns |
| https://doi.org/10.1093/cid/ciy1143 | The Path to Group A Streptococcus Vaccines: World Health Organization Research and Development Technology Roadmap and Preferred Product Characteristics |
| https://doi.org/10.1016/j.jpeds.2003.10.024 | Posttraumatic stress disorder after dog bites in children |
| https://doi.org/10.1093/humrep/deu158 | Safety and usefulness of cryopreservation of ovarian tissue to preserve fertility: a 12-year retrospective analysis |
| https://doi.org/10.1002/pbc.25608 | Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment |
| https://doi.org/10.1016/j.bja.2021.02.016 | Morbidity and mortality after anaesthesia in early life: results of the European prospective multicentre observational study, neonate and children audit of anaesthesia practice in Europe (NECTARINE) |
| https://doi.org/10.1111/j.1365-2222.2009.03292.x | Basophil activation tests for the diagnosis of food allergy in children |
| https://doi.org/10.1016/j.ajic.2016.11.026 | Antibiotic knowledge and self-medication practices in a developing country: A cross-sectional study |
| https://doi.org/10.1213/ane.0b013e31817e6eac | The Effects of Hydroxyethyl Starch 130/0.4 (6%) on Blood Loss and Use of Blood Products in Major Surgery: A Pooled Analysis of Randomized Clinical Trials |
| https://doi.org/10.1073/pnas.1816143116 | Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency |
| https://doi.org/10.1038/s41436-018-0420-y | ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants |
| https://doi.org/10.1007/5584_2019_357 | Epidemiology, Diagnosis and Risk Factors of Helicobacter pylori Infection |
| https://doi.org/10.1007/s00467-012-2131-y | Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics |