Autosomal Dominant Tubulointerstitial Kidney Disease Latest Advances

Autosomal Dominant Tubulo-Interstitial Kidney Disease: Approach to Diagnosis.

Journal: Advances in kidney disease and health

Published: May 23, 2026

A novel and two recurrent UMOD mutations in autosomal dominant tubulointerstitial kidney disease (ADTKD): a case series and literature review.

Journal: Renal failure

Published: April 10, 2026

Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD: Case Report and Disease Update.

Journal: Diagnostics (Basel, Switzerland)

Published: April 01, 2026

MANF Clears Mutant Uromodulin in Human Kidney Organoids of Autosomal Dominant Tubulointerstitial Kidney Disease.

Journal: bioRxiv : the preprint server for biology

Published: March 23, 2026

A Partial UMOD Deletion Results in Altered Uromodulin Synthesis and Autosomal-Dominant Tubulointerstitial Kidney Disease-Uromodulin.

Journal: Kidney medicine

Published: March 09, 2026

Rapidly Progressive Kidney Failure With Transient Non-Cystic Kidney Enlargement: A Case Report Highlighting Delayed Medullary Cyst Formation.

Journal: Nephrology (Carlton, Vic.)

Published: January 20, 2026

Thin Glomerular Basement Membrane Phenotypes With No Identified Pathogenic COL4A3/A4/A5 Variant.

Journal: Kidney international reports

Published: January 11, 2026

Clinical and Molecular characteristics of kidney and urinary tract congenital anomalies in a cohort of Egyptian patients using whole-exome sequencing.

Journal: Molecular biology reports

Published: January 02, 2026

Calorie Restriction Leads to Degradation of Mutant Uromodulin and Ameliorates Inflammation and Fibrosis in UMOD -Related Kidney Disease.

Journal: Journal of the American Society of Nephrology : JASN

Published: December 18, 2025

De novo SEC61A1 mutation in congenital anemia and early-onset kidney disease: Case report and review of the literature.

Journal: Gene

Published: December 17, 2025

Lipocalin-2 Is Induced by Uromodulin Aggregates without Affecting Kidney Disease Progression in Autosomal Dominant Tubulointerstitial Kidney Disease- UMOD.

Journal: Journal of the American Society of Nephrology : JASN

Published: November 28, 2025

A case of ADTKD-UMOD presenting with focal segmental glomerulosclerosis in a young male with a positive family history.

Journal: BMC nephrology

Published: October 28, 2025

Autosomal Dominant Tubulointerstitial Kidney Disease Latest Advances

Find the Latest Research About Autosomal Dominant Tubulointerstitial Kidney Disease

Autosomal Dominant Tubulo-Interstitial Kidney Disease: Approach to Diagnosis.

Autosomal Dominant Tubulo-Interstitial Kidney Disease: Approach to Diagnosis.

A novel and two recurrent UMOD mutations in autosomal dominant tubulointerstitial kidney disease (ADTKD): a case series and literature review.

A novel and two recurrent UMOD mutations in autosomal dominant tubulointerstitial kidney disease (ADTKD): a case series and literature review.

Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD: Case Report and Disease Update.

Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD: Case Report and Disease Update.

MANF Clears Mutant Uromodulin in Human Kidney Organoids of Autosomal Dominant Tubulointerstitial Kidney Disease.

MANF Clears Mutant Uromodulin in Human Kidney Organoids of Autosomal Dominant Tubulointerstitial Kidney Disease.

A Partial UMOD Deletion Results in Altered Uromodulin Synthesis and Autosomal-Dominant Tubulointerstitial Kidney Disease-Uromodulin.

A Partial UMOD Deletion Results in Altered Uromodulin Synthesis and Autosomal-Dominant Tubulointerstitial Kidney Disease-Uromodulin.

Rapidly Progressive Kidney Failure With Transient Non-Cystic Kidney Enlargement: A Case Report Highlighting Delayed Medullary Cyst Formation.

Rapidly Progressive Kidney Failure With Transient Non-Cystic Kidney Enlargement: A Case Report Highlighting Delayed Medullary Cyst Formation.

Thin Glomerular Basement Membrane Phenotypes With No Identified Pathogenic COL4A3/A4/A5 Variant.

Thin Glomerular Basement Membrane Phenotypes With No Identified Pathogenic COL4A3/A4/A5 Variant.

Clinical and Molecular characteristics of kidney and urinary tract congenital anomalies in a cohort of Egyptian patients using whole-exome sequencing.

Clinical and Molecular characteristics of kidney and urinary tract congenital anomalies in a cohort of Egyptian patients using whole-exome sequencing.

Calorie Restriction Leads to Degradation of Mutant Uromodulin and Ameliorates Inflammation and Fibrosis in UMOD -Related Kidney Disease.

Calorie Restriction Leads to Degradation of Mutant Uromodulin and Ameliorates Inflammation and Fibrosis in UMOD -Related Kidney Disease.

De novo SEC61A1 mutation in congenital anemia and early-onset kidney disease: Case report and review of the literature.

De novo SEC61A1 mutation in congenital anemia and early-onset kidney disease: Case report and review of the literature.

Lipocalin-2 Is Induced by Uromodulin Aggregates without Affecting Kidney Disease Progression in Autosomal Dominant Tubulointerstitial Kidney Disease- UMOD.

Lipocalin-2 Is Induced by Uromodulin Aggregates without Affecting Kidney Disease Progression in Autosomal Dominant Tubulointerstitial Kidney Disease- UMOD.

A case of ADTKD-UMOD presenting with focal segmental glomerulosclerosis in a young male with a positive family history.

A case of ADTKD-UMOD presenting with focal segmental glomerulosclerosis in a young male with a positive family history.