N. Godefroid

发表

Abstracts presented at the 23rd Annual Congress of the Belgian Society of Internal Medicine, 14–15 December 2018, Dolce La Hulpe, La Hulpe, Belgium

D. Abramowicz, K. Dahan, K. Claes, 2018, Acta clinica Belgica.

Prevalence of Hypertension in Children with Early-Stage ADPKD.

R. Salomon, M. Mizerska-Wasiak, D. Mekahli, 2018, Clinical journal of the American Society of Nephrology : CJASN.

Children of non-Western origin with end-stage renal disease in the Netherlands, Belgium and a part of Germany have impaired health-related quality of life compared with Western children.

J. H. van der Lee, J. Groothoff, M. Van Dyck, 2014, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Autosomal dominant polycystic kidney disease is associated with central and nephrogenic defects in osmoregulation.

J. Haymann, A. Serra, O. Devuyst, 2012, Kidney international.

Evidence for Bone and Mineral Metabolism Alterations in Children With Autosomal Dominant Polycystic Kidney Disease

D. Mekahli, J. Bacchetta, E. Levtchenko, 2017, The Journal of clinical endocrinology and metabolism.

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

A. Anarat, S. Schmidt, S. Testa, 2018, The Journal of pediatrics.

Important differences in management policies for children with end-stage renal disease in the Netherlands and Belgium--report from the RICH-Q study.

J. H. van der Lee, J. Groothoff, M. Offringa, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Dietary Fibre Intake Is Associated with Serum Levels of Uraemic Toxins in Children with Chronic Kidney Disease

W. van Biesen, M. Van Dyck, G. Glorieux, 2021, Toxins.

Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene.

P. Houillier, X. Jeunemaître, R. Salomon, 2006, Journal of the American Society of Nephrology : JASN.

Dietary fibre intake is low in paediatric chronic kidney disease patients but its impact on levels of gut-derived uraemic toxins remains uncertain

W. van Biesen, M. Van Dyck, G. Glorieux, 2021, Pediatric Nephrology.

Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.

K. Dahan, N. Godefroid, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Cinacalcet sustainedly prevents pancreatitis in a child with a compound heterozygous SPINK1/AP2S1 mutation.

Y. Pirson, E. Sokal, X. Stephenne, 2019, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Corticosteroid-free Kidney Transplantation Improves Growth: 2-Year Follow-up of the TWIST Randomized Controlled Trial

M. McCulloch, D. Milford, S. Roberts, 2015, Transplantation.

Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium

G. Mortier, B. Bravenboer, E. Levtchenko, 2021, Frontiers in Endocrinology.

Haemolytic uremic syndrome surveillance in children less than 15 years in Belgium, 2009–2015

D. Piérard, M. Sabbe, K. Van Hoeck, 2018, Archives of Public Health.

A girl with rickets and nephrocalcinosis

W. Proesmans, N. Godefroid, 2003, Pediatric Nephrology.

Lessons learned from efforts to improve the quality of care in children with end-stage renal disease in the Netherlands and Belgium

J. H. van der Lee, J. Groothoff, M. Offringa, 2011, Archives of Disease in Childhood.

Epstein-Barr Virus-associated Pulmonary Tumor: A Pediatric Case and Discussion of the Literature

A. Poncelet, A. Froidure, N. Godefroid, 2021, Journal of pediatric hematology/oncology.

Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.

A. Vénisse, K. Dahan, X. Jeunemaître, 2018, Kidney international.

Transplantation for Primary Hyperoxaluria Type 1: Designing New Strategies in the Era of Promising Therapeutic Perspectives

P. Cochat, A. Devresse, N. Kanaan, 2020, Kidney international reports.

18F-Fluorodeoxyglucose Positron Emission Tomography: a Useful Tool for the Diagnosis of Endocarditis in a Boy with Congenital Heart Disease: a Case Report

A. Poncelet, V. Roelants, P. Baldin, 2021, SN Comprehensive Clinical Medicine.

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-EDTA) Registry.

D. Mekahli, T. Seeman, A. Jankauskienė, 2016, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.

H. Debaix, P. Houillier, B. Knebelmann, 2021, Journal of the American Society of Nephrology : JASN.

Considerations for prenatal counselling of patients with cardiac rhabdomyomas based on their cardiac and neurologic outcomes

T. Sluysmans, C. Vermylen, C. Chantrain, 2018 .

Development of renal and iliac aneurysms in a child with generalized infantile myofibromatosis

T. Sluysmans, C. Vermylen, C. Chantrain, 2010, Pediatric Nephrology.

Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

K. Dahan, O. Devuyst, J. Hoenderop, 2007, Journal of the American Society of Nephrology : JASN.

A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.

K. Dahan, O. Devuyst, C. Saint-Martin, 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in platelets.

Chantal Thys, Kathleen Freson, F. de Zegher, 2008, The Journal of clinical endocrinology and metabolism.

vWFpp/ADAMTS13 ratio is a useful marker of postliver transplantation thrombotic microangiopathy: A pediatric case report

E. Sokal, M. Komuta, R. Reding, 2019, Clinical case reports.

Belgian consensus statement on the diagnosis and management of patients with atypical hemolytic uremic syndrome

D. Abramowicz, K. Dahan, L. P. Van den Heuvel, 2018, Acta clinica Belgica.

mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy

D. Sabatini, E. Schulze-Bahr, B. Schermer, 2021, Journal of the American Society of Nephrology : JASN.

Clinical characteristics and outcomes of children with stage 3–5 chronic kidney disease

F. Collart, A. Robert, K. Ismaili, 2010, Pediatric Nephrology.

Disparities in dialysis treatment and outcomes for Dutch and Belgian children with immigrant parents

J. H. van der Lee, J. Groothoff, M. Lilien, 2012, Pediatric Nephrology.

Fewer pre-emptive renal transplantations and more rejections in immigrant children compared to native Dutch and Belgian children.

J. H. van der Lee, J. Groothoff, M. Lilien, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Uremic Toxin Concentrations are Related to Residual Kidney Function in the Pediatric Hemodialysis Population

W. van Biesen, R. Vanholder, M. Litwin, 2019, Toxins.

Dynamics of hospitalizations in hemodialysis patients : results from a large US provider

J. Groothoff, M. Grootenhuis, L. Haverman, 2014 .

ANCA vasculitis in a patient with Alport syndrome: a difficult diagnosis but a treatable disease!

M. Jadoul, S. Aydın, N. Godefroid, 2017, BMC Nephrology.

Presentation and management of mycotic pseudoaneurysm after kidney transplantation

M. Mourad, R. Verhelst, D. Patrono, 2015, Transplant infectious disease : an official journal of the Transplantation Society.

Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report

R. Reding, F. Fusaro, N. Godefroid, 2015, Journal of Medical Case Reports.

Severe parental phenotype associates with hypertension in children with ADPKD

K. Dahan, N. Demoulin, J. Morelle, 2023, Pediatric Nephrology.

Two‐step transplantation for primary hyperoxaluria: Cadaveric liver followed by living donor related kidney transplantation

I. Malla, E. Sokal, R. Reding, 2009, Pediatric transplantation.

ADPedKD: A Global Online Platform on the Management of Children With ADPKD

R. Salomon, M. Gafencu, C. Stoica, 2019, Kidney international reports.

mTOR-activating mutations in RRAGD cause kidney tubulopathy and cardiomyopathy (KICA) syndrome

D. Sabatini, E. Schulze-Bahr, B. Schermer, 2021, bioRxiv.

Characterization, evolution and risk factors of diabetes and prediabetes in a pediatric cohort of renal and liver transplant recipients

A. Robert, E. Sokal, R. Reding, 2023, Frontiers in Pediatrics.

Accumulation of uraemic toxins is reflected only partially by estimated GFR in paediatric patients with chronic kidney disease

W. van Biesen, R. Vanholder, M. Van Dyck, 2018, Pediatric Nephrology.

Low rates of humoral response to BNT162b2 SARS-CoV-2 vaccination in patients with immune-mediated kidney diseases treated with rituximab

M. Jadoul, N. Demoulin, J. Morelle, 2021, Clinical kidney journal.

Typical or Atypical Hemolytic Uremic Syndrome and the Use of Eculizumab: 4 Illustrative Cases.

T. Detaille, Maëlle de Ville de Goyet, N. Godefroid, 2019, Journal of pediatric hematology/oncology.

D. Mekahli, E. Levtchenko, S. Eloot, 2023, Pediatric Nephrology.

Liver Transplantation in Primary Hyperoxaluria Type 1: We Have to Find an Alternative!

E. Sokal, R. Reding, X. Stephenne, 2021, Transplantation.

18‐Fluorodeoxyglucose positron emission computed tomography for systemic oxalosis in primary hyperoxaluria type 1

R. Lhommel, A. Devresse, N. Kanaan, 2021, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Lessons for the clinical nephrologist: lumasiran as the future cornerstone treatment for patients with primary hyperoxaluria type 1?

K. Dahan, A. Devresse, A. Scohy, 2022, Journal of Nephrology.

Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies

K. Dahan, E. Levtchenko, C. Lambert, 2023, Clinical journal of the American Society of Nephrology : CJASN.