Bartter Syndrome Latest Advances
Find the Latest Research About Bartter Syndrome
Last Updated: 06/30/2026
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Found 1789 publications
Molecular Genetics of Bartter Syndrome: Bridging Genotype-Phenotype Correlations and Precision Therapeutics.
Journal: Current issues in molecular biology
Published: March 16, 2026
Case Report: Anesthesia for emergent gastroscopy in a pediatric patient with Bartter's syndrome.
Journal: Frontiers in medicine
Published: March 06, 2026
A dual-organ genetic interplay between sensorineural hearing loss and kidney disease: an update for clinicians.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 30, 2026
The Importance of Molecular Testing in the Diagnosis of Genetic Syndromes with Chronic Kidney Disease: Genotype-Phenotype Correlations.
Journal: International journal of molecular sciences
Published: January 22, 2026
A newborn with type 1 Bartter syndrome: challenges in the treatment and development during 30 months follow-up-a case report.
Journal: Frontiers in pediatrics
Published: December 21, 2025
Acute Kidney Injury in Children with Polyuria: A Systematic Review.
Journal: Journal of clinical medicine
Published: December 05, 2025
Two Cases of Prenatally Suspected Fetal Bartter Syndrome With a Novel Genetic Variant Indicated by Polyhydramnios and Amniotic Fluid Biochemistry.
Journal: Congenital anomalies
Published: November 23, 2025
Transient antenatal Bartter syndrome type 5 presenting as shock and metabolic acidosis in a preterm neonate.
Journal: Pediatric nephrology (Berlin, Germany)
Published: October 04, 2025
Severe Recurrent Polyhydramnios as a Prenatal Signal of MAGED2-Related Bartter Syndrome: A Clinical Perspective.
Journal: Clinical medicine insights. Pediatrics
Published: September 26, 2025
Last Updated: 06/30/2026