Nephrocalcinosis Latest Advances

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

Published: March 06, 2026

A Modern-Day Captain Charles Martell: Catastrophic Skeletal Manifestations of Primary Hyperparathyroidism.

Journal: Case reports in endocrinology

Published: February 24, 2026

ATP6V1B1-Associated Inherited Distal Renal Tubular Acidosis in Children: Insights from a Literature Review.

Journal: Children (Basel, Switzerland)

Published: February 23, 2026

Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice.

Journal: Cells

Published: February 13, 2026

Nephrocalcinosis Latest Advances

Find the Latest Research About Nephrocalcinosis

Kidney imaging for the diagnosis and follow-up of a primary hyperoxaluria type 1 patient with NC, NL, and severe chronic kidney disease: a case report with literature review.

Kidney imaging for the diagnosis and follow-up of a primary hyperoxaluria type 1 patient with NC, NL, and severe chronic kidney disease: a case report with literature review.

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Thiazide therapy in chronic hypoparathyroidism: effects on hypercalciuria and renal function-a systematic review and exploratory meta-analysis.

Thiazide therapy in chronic hypoparathyroidism: effects on hypercalciuria and renal function-a systematic review and exploratory meta-analysis.

Three People With Recurrent Nephrolithiasis and Heterozygous ABCC6 Mutations.

Three People With Recurrent Nephrolithiasis and Heterozygous ABCC6 Mutations.

Nephrocalcinosis and Foam Cell-Rich Medullary Interstitial Nephropathy in a Patient with Laxative-Induced Hypokalemia: A Case Report.

Nephrocalcinosis and Foam Cell-Rich Medullary Interstitial Nephropathy in a Patient with Laxative-Induced Hypokalemia: A Case Report.

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine.

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine.

Heterogeneous Phenotypes of Primary Hyperparathyroidism in Romania: Characterization of a Large Cohort.

Heterogeneous Phenotypes of Primary Hyperparathyroidism in Romania: Characterization of a Large Cohort.

Bowing Bones and Nephrocalcinosis in a Young Male.

Bowing Bones and Nephrocalcinosis in a Young Male.

The European distal renal tubular acidosis registry: a five-year analysis.

The European distal renal tubular acidosis registry: a five-year analysis.

A Modern-Day Captain Charles Martell: Catastrophic Skeletal Manifestations of Primary Hyperparathyroidism.

A Modern-Day Captain Charles Martell: Catastrophic Skeletal Manifestations of Primary Hyperparathyroidism.

ATP6V1B1-Associated Inherited Distal Renal Tubular Acidosis in Children: Insights from a Literature Review.

ATP6V1B1-Associated Inherited Distal Renal Tubular Acidosis in Children: Insights from a Literature Review.

Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice.

Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice.