• Association of DiGeorge anomaly and caudal dysplasia sequence in a neonate born to a diabetic mother
• Bardet-Biedl syndrome: a case series
• Cadmium Induces Kidney Iron Deficiency and Chronic Kidney Injury by Interfering with the Iron Metabolism in Rats
• Clinical features of 102 patients with different types of Herlyn-Werner-Wunderlich syndrome
• Comparative Effects of Irreversible Electroporation, Radiofrequency Ablation, and Partial Nephrectomy on Renal Function Preservation in a Porcine Solitary Kidney Model
• Diagnostic challenges of hemihematocolpos and dysmenorrhea in adolescents: obstructed hemivagina, didelphys or bicornuate uterus and renal aplasia is a rare female genital malformation
• Endoscopic description of renal papillary abnormalities in stone disease by flexible ureteroscopy: a proposed classification of severity and type
• Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
• Hereditary renal adysplasia in a three generations family
• HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes
• Mutant HRas Signaling and Rationale for Use of Farnesyltransferase Inhibitors in Head and Neck Squamous Cell Carcinoma
• Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice
• Renal abnormalities associated with Mayer-Rokitansky-Küster-Hauser syndrome
• Renoprotective effects of oleanolic acid and its possible mechanisms in rats with diabetic kidney disease
• The presentation and management of complex female genital malformations