Last Updated: 09/26/2026
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Found 9 publications
Association of Rare Variants in Kidney Developmental Genes With Chronic Kidney Disease and Blood Pressure: A UK Biobank Study.
Journal: WMJ : official publication of the State Medical Society of Wisconsin
Published: April 22, 2025
Total plasma cfDNA methylation in pediatric kidney transplant recipients provides insight into acute allograft rejection pathophysiology.
Journal: Clinical immunology (Orlando, Fla.)
Published: December 23, 2024
Methylation patterns of the nasal epigenome of hospitalized SARS-CoV-2 positive patients reveal insights into molecular mechanisms of COVID-19.
Journal: BMC medical genomics
Published: September 03, 2024
The methylome and cell-free DNA: current applications in medicine and pediatric disease.
Journal: Pediatric research
Published: May 16, 2022
A rare cause of oligoanuric kidney failure - a diagnosis not to miss: Answers.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 31, 2022
A rare cause of oligoanuric kidney failure - a diagnosis not to miss: Questions.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 11, 2022
Induction of calcitonin gene-related peptide expression in rats by cortical spreading depression.
Journal: Cephalalgia : an international journal of headache
Published: December 06, 2016
Bladder Neck Contracture Following Radical Retropubic versus Robotic-Assisted Laparoscopic Prostatectomy.
Journal: Current urology
Published: September 09, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026