Albertien M. Van Eerde - Publications

Primary hyperoxaluria type 1-current practice in the siRNA era: an ERA Genes & Kidney Working Group survey.

Journal: Clinical kidney journal

Published: December 05, 2025

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Journal: Nature communications

Published: October 09, 2025

Transition of patients with hereditary nephropathies from paediatric to adult care.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: June 18, 2025

10 tips on how to take a proper family history in CKD patient care.

Journal: Clinical kidney journal

Published: June 04, 2025

Chronic Kidney Disease of unexplained cause (CKDx): a consensus statement by the Genes & Kidney Working Group of the ERA.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: January 18, 2025

Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet).

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 14, 2025

Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 13, 2025

Biallelic TMEM72 Variants in Patients with a Nephronophthisis-Like Phenotype.

Journal: Nephron

Published: December 21, 2024

Pregnancy and Long-Term Kidney Function in CKD: A Systematic Review and Meta-Analysis.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: December 09, 2024

Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Journal: Nature communications

Published: November 16, 2024

Diagnosis, management and treatment of the Alport syndrome - 2024 guideline on behalf of ERKNet, ERA and ESPN.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: September 30, 2024

The Role of Genetic Testing in Adult CKD.

Journal: Journal of the American Society of Nephrology : JASN

Published: September 17, 2024