Disease: Urogenital adysplasia
- 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 <sup>99m</sup>Tc-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