Ilse M. Rood - Publications

mRNA Sequencing to Identify Aberrant Splicing in X-linked Alport Syndrome.

Journal: Kidney international reports

Published: June 25, 2025

Urinary carbonic anhydrase 1 as a marker of hematuria in IgA nephropathy.

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

Published: April 30, 2025

Corrigendum: Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review.

Journal: Frontiers in endocrinology

Published: December 19, 2023

Kidney Disease Associated With Mono-allelic COL4A3 and COL4A4 Variants: A Case Series of 17 Families.

Journal: Kidney medicine

Published: March 17, 2023

Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review.

Journal: Frontiers in endocrinology

Published: February 17, 2023

Later Response to Corticosteroids in Adults With Primary Focal Segmental Glomerular Sclerosis Is Associated With Favorable Outcomes.

Journal: Kidney international reports

Published: August 27, 2021

Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix in Collapsing Focal Segmental Glomerulosclerosis.

Journal: Journal of the American Society of Nephrology : JASN

Published: July 14, 2019

NMR and MS urinary metabolic phenotyping in kidney diseases is fit-for-purpose in the presence of a protease inhibitor.

Journal: Molecular omics

Published: January 24, 2019

In Reply to 'Critical Considerations in Genetic Counseling of Patients With the NPHS2 R229Q Variant'.

Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation

Published: December 10, 2018

Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.

Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation

Published: March 21, 2018

Isolation and characterization of urinary extracellular vesicles: implications for biomarker discovery.

Journal: Nature reviews. Nephrology

Published: October 31, 2017

Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome.

Journal: The Netherlands journal of medicine

Published: March 09, 2016