• A cross-sectional study of the genital duct and renal anomalies in Egyptian cases of congenital absence of the vas deferens
• A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis
• A proteoglycan isolated from Ganoderma lucidum attenuates diabetic kidney disease by inhibiting oxidative stress-induced renal fibrosis both in vitro and in vivo
• A very rare syndrome and its rare urological complication: Incomplet bladder duplication in Robinow syndrome
• Analysis of the effect of ultrasonography in detecting fetal congenital renal malformation
• Anhydramnios in the Setting of Renal Malformations: The National Institutes of Health Workshop Summary
• Antenatal nephromegaly and propionic acidemia: a case report
• Association of DiGeorge anomaly and caudal dysplasia sequence in a neonate born to a diabetic mother
• Bardet-Biedl syndrome: a case series
• Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities
• Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus
• Cardiorespiratory fitness and sports activities in children and adolescents with solitary functioning kidney
• Cardiorespiratory fitness: a comparison between children with renal transplantation and children with congenital solitary functioning kidney
• CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies
• Clinical and genetic analysis of a newborn with hypoparathyroidism, sensorineural hearing loss, and renal dysplasia syndrome
• Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome
• Combination of debulking single-tract percutaneous nephrolithotomy followed by retrograde intrarenal surgery for staghorn stones in solitary kidneys
• Comparative Effects of Irreversible Electroporation, Radiofrequency Ablation, and Partial Nephrectomy on Renal Function Preservation in a Porcine Solitary Kidney Model
• Comparison of 2 Computed Tomography-based Methods to Estimate Preoperative and Postoperative Renal Parenchymal Volume and Correlation With Functional Changes After Partial Nephrectomy
• Comparison of perioperative outcomes of robot-assisted partial nephrectomy and open partial nephrectomy in patients with a solitary kidney
• Comparison of shockwave lithotripsy and flexible ureteroscopy for the treatment of kidney stones in patients with a solitary kidney
• Congenital abnormalities of the urogenital tract: the clue is in the cord?
• Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT)
• Congenital Unilateral Renal Aplasia in a Cynomolgus Monkey (<em>Macaca fascicularis</em>) With Investigation Into Potential Pathogenesis
• Conservative Treatment of Didelphyc Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis
• Contemporary Imaging Practice Patterns Following Ureteroscopy for Stone Disease
• Diagnostic approach to chronic kidney disease
• Diagnostic challenges of hemihematocolpos and dysmenorrhea in adolescents: obstructed hemivagina, didelphys or bicornuate uterus and renal aplasia is a rare female genital malformation
• Doege Potter syndrome presenting as multiple fibrous tumours of the chest
• Doege-Potter syndrome in a patient with a giant abdominal solitary fibrous tumor: a case report and review of the literature
• Does a Ureteral Obstruction Affect the Contralateral Kidney Morphology? A Stereological Analysis in a Rodent Model
• Effect of Renal Reconstruction on Renal Function After Partial Nephrectomy
• Endoscopic description of renal papillary abnormalities in stone disease by flexible ureteroscopy: a proposed classification of severity and type
• Endoscopic Evidence That Randall's Plaque is Associated with Surface Erosion of the Renal Papilla
• Evaluation of hypertension by ambulatory blood pressure monitoring in children with solitary kidney
• Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
• Fluid flow shear stress over podocytes is increased in the solitary kidney
• Four miniature kidneys: supernumerary kidney and multiple organ system anomalies
• Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome
• GDF11, a target of miR-32-5p, suppresses high-glucose-induced mitochondrial dysfunction and apoptosis in HK-2 cells through PI3K/AKT signaling activation
• Genomic profile - a possible diagnostic and prognostic marker in upper tract urothelial carcinoma
• Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis
• GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndrome
• Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report
• Hereditary urogenital adysplasia
• Histopathology in Ureteropelvic Junction Obstruction With and Without Crossing Vessels
• HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes
• Hysteroscopic management of an oblique vaginal septum in a virgin girl with a rare variant of Herlyn-Werner-Wunderlich syndrome
• Incidental finding of Zinner syndrome in a Greek military recruit: a case report of a rare clinical entity
• Inflammation and oxidative stress in viper bite: an insight within and beyond
• Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans
• Intestinal SIRT1 Deficiency-Related Intestinal Inflammation and Dysbiosis Aggravate TNFα-Mediated Renal Dysfunction in Cirrhotic Ascitic Mice
• Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis
• Kidney biopsy in patients with antineutrophil cytoplasmic antibody-associated vasculitis with mild renal abnormality
• Long-term impact of unilateral hypo/dysplastic kidney in infants with primary vesicoureteral reflux
• Longitudinal vaginal septa with associated uterine anomalies: a case series
• Loss of a kidney during fetal life: long-term consequences and lessons learned
• Magnetic resonance imaging for evaluation of foetal multicystic dysplastic kidney
• Mullerian anomalies and renal agenesis: autosomal dominant urogenital adysplasia
• Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice
• Nephron Deficiency and Predisposition to Renal Injury in a Novel One-Kidney Genetic Model
• New tubular injury markers in children with a solitary functioning kidney
• Non-papillary prone percutaneous nephrolithotomy for renal abnormalities: single-institution experience
• Obstructed Hemivagina with Ipsilateral Renal Anomaly
• Oligohydramnios sequence revisited in relationship to arthrogryposis, with distinctive skin changes
• Ovarian absence: a systematic literature review and case series report
• Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome
• Percutaneous microwave ablation of renal cell carcinoma is safe in patients with a solitary kidney
• Perinatal and infant outcome of fetuses with prenatally diagnosed hyperechogenic kidneys
• Predicting congenital renal tract malformation genes using machine learning
• Prenatal and Early Postnatal Outcomes for Fetuses with Anatomic or Functional Renal Agenesis
• Prenatal Diagnosis of Fetal Obstructed Hemivagina and Ipsilateral Renal Agenesis (OHVIRA) Syndrome
• Prevalence of Renal and Cervical Vertebral Anomalies in Patients With Isolated Microtia and/or Aural Atresia
• Prospective Study on Several Urinary Biomarkers as Indicators of Renal Damage in Children with CAKUT
• Recurrent clot anuria following laparoscopic pyeloplasty in a solitary functioning kidney: managing with double guide wire technique
• Renal abnormalities among children with sickle cell conditions in highly resource-limited setting in Ghana
• Renal abnormalities associated with Mayer-Rokitansky-Küster-Hauser syndrome
• Renal oligo- and anhydramnios: cause, course and outcome--a single-center study
• Renal tract abnormalities missed in a historical cohort of young children with UTI if the NICE and AAP imaging guidelines were applied
• Renoprotective effects of oleanolic acid and its possible mechanisms in rats with diabetic kidney disease
• Requirement for a uroplakin 3a-like protein in the development of zebrafish pronephric tubule epithelial cell function, morphogenesis, and polarity
• Robot-assisted laparoscopic pyeloplasty is a valid option for ureteropelvic junction obstruction repair in adults with congenital renal abnormalities: a case series study
• Safety and efficacy of partial nephrectomy for solitary kidney tumor
• Semi-quantification of renal perfusion using ^99mTc-DTPA in systolic heart failure: a feasibility study
• Shockwave Lithotripsy Practice Pattern Variations Among and Between American and Canadian Urologists: In Support of Guidelines
• Short-term functional and oncological outcomes of partial nephrectomy for renal cell carcinoma in patients with an anatomically or functionally solitary kidney: single-center experience
• Sirenomelia, renal agenesis and normal amniotic fluid volume
• STAR syndrome plus: The first description of a female patient with the lethal form
• Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report
• Targeting-intratumoral-lactic-acidosis transcatheter-arterial-chemoembolization for non-islet cell tumor hypoglycemia secondary to a liver metastatic solitary fibrous tumor: A case report and literature review
• Termination of pregnancy due to renal tract abnormalities: survey of 97 fetuses from a single medical center
• The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome
• The Neuropathology of 1p36 Deletion Syndrome: An Autopsy Case Series
• The presentation and management of complex female genital malformations
• Transitional cell carcinoma of ureter in a solitary functioning kidney
• Uncovering risk factors for kidney injury in children with a solitary functioning kidney
• Unilateral macrocystic dysplasia and contralateral agenesis in a monoamniotic twin
• Unusual case of OHVIRA syndrome with a single uterus, unrecognized before labor and followed by an intrapartal rupture of obstructed hemivagina
• Uric acid and hypertension: a focused review and practical recommendations
• Urogenital development in Pallister-Hall syndrome is disrupted in a cell-lineage-specific manner by constitutive expression of GLI3 repressor