• [18F]-PSMA-1007-PET for evaluation of kidney function
• A machine learning algorithm predicting risk of dilating VUR among infants with hydronephrosis using UTD classification
• A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcysts
• A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis
• A rare case of Doege-Potter Syndrome caused by recurrent solitary fibrous tumor of the pleura
• A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings
• A rare middle aortic syndrome with celiac trunk, superior mesenteric and bilateral renal artery involvement
• A rare variant of obstructed hemivagina and ipsilateral renal agenesis and its improvement of classification
• A renal aplasia case mimicking radiologically as unilateral renal agenesis in a child with spina bifida, atresia ani and unilateral undescended testis: a case report
• Adolescent abdominal pain due to rare mullerian duct anomaly
• Adult-Onset IgA Vasculitis Associated With Pulmonary-Renal Syndrome Following COVID-19 Infection: A Case Report and Literature Review
• Angiotensin-II Use for Refractory Hypotension in an Infant With Bilateral Renal Agenesis
• Are weight or age limits for pediatric laparoscopic pyeloplasty? Results of a multicentric study
• Artificial Urinary Sphincter With Bilateral Atrophic Kidneys and Accessory Renal Arteries in a Male Cadaveric Subject: A Case Report and Clinicopathological Reconciliation of Urinary Abnormalities and Embryogenetic Correlation of Vascular Aberrations
• Assessment of fluid status in neonatal dialysis: the need for new tools
• Bi-allelic pathogenic variants in ITGA8 cause slowly progressive renal disease of unknown etiology
• Bicornuate bicollis uterus with right cervical stenosis and ipsilateral renal agenesis
• Bilateral Renal Agenesis-Interpreting the RAFT Trial
• Bilateral renal agenesis: fetal intervention and outcomes
• Bilateral Renal Ectopia-Prenatal Diagnosis
• Case report: Crossed fused renal ectopia with stones: A surgical challenge overcome by robotic surgery
• Case Report: Non-ossifying fibromas with pathologic fractures in a patient with <em>NONO</em>-associated X-linked syndromic intellectual developmental disorder
• Clinical and molecular characteristics of two Italian kindreds with hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome
• Clinical features of 102 patients with different types of Herlyn-Werner-Wunderlich syndrome
• Comparison of Serial Amnioinfusion Strategies for Isolated Early-Onset Fetal Renal Anhydramnios
• Conservative Treatment of Didelphyc Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis
• Cystic dysplasia of the rete testis accompanying ipsilateral renal agenesis in a young adult: a case report
• Denosumab-induced hypocalcemia post bariatric surgery-a severe and protracted course: a case report
• Deruxtecan-Induced Reversible Fanconi Syndrome
• Design and Protocol of the Renal Anhydramnios Fetal Therapy (RAFT) Trial
• Detection of non-cardiac fetal abnormalities by ultrasound at 11-14 weeks: systematic review and meta-analysis
• Detection of non-cardiac fetal abnormalities on ultrasound at 11-14 weeks: systematic review and meta-analysis
• Detection rates of a national fetal anomaly screening programme: A national cohort study
• Doege Potter syndrome presenting as multiple fibrous tumours of the chest
• DOEGE-POTTER SYNDROME BY PLEURAL SOLITARY FIBROUS TUMOR
• Doege-Potter syndrome due to a hepatic solitary fibrous tumour
• Doege-Potter syndrome in a patient with a giant abdominal solitary fibrous tumor: a case report and review of the literature
• Doege-Potter Syndrome; A Case of Solitary Fibrous Pleura Tumor Associated with Severe Hypoglycemia: A Case Report in Internal Medicine
• Early diagnosis of solitary functioning kidney: comparing the prognosis of kidney agenesis and multicystic dysplastic kidney
• Effective management of recurrent Doege-Potter syndrome with somatostatin-analogues: A case report
• Epidemiological Patterns of Cannabis- and Substance- Related Congenital Uronephrological Anomalies in Europe: Geospatiotemporal and Causal Inferential Study
• Fetal Nephrology: A Quaternary Care Center Experience
• Fetal Therapy for Renal Anhydramnios
• Fraser syndrome with limb reduction defect: a rare and unique anatomic variation
• Generalized arterial calcification of infancy in a neonate with acute kidney injury: A rare case report
• Hemihysterectomy in a patient with uterus didelphys, vaginal septum and ipsilateral renal agenesis: A case report and literature review
• Herlyn-Werner-Wunderlinch: An unusual presentation in a patient with Prader-Willi syndrome
• Icteric Leptospirosis Leading to Multiorgan Failure and Concomitant Pancreatitis
• Laparoscopy combined with transvaginal surgery for Herlyn-Werner-Wunderlich syndrome: A case report
• Long-Term Outcomes, Including Fetal and Neonatal Prognosis, of Renal Oligohydramnios: A Retrospective Study over 22 Years
• Missense Variants in <em>GFRA1</em> and <em>NPNT</em> Are Associated with Congenital Anomalies of the Kidney and Urinary Tract
• Neonatal Survival After Serial Amnioinfusions for Bilateral Renal Agenesis: The Renal Anhydramnios Fetal Therapy Trial
• Nonfamilial VACTERL-H Syndrome in a Dizygotic Twin: Prenatal Ultrasound and Postnatal 3D CT Findings
• Now what: navigating care of maternal/fetal dyads with bilateral renal agenesis after RAFT. A physician and parent point of view
• Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome: A Case Report
• Obstructed Hemivagina Ipsilateral Renal Agenesis (OHVIRA) Syndrome-A Retrospective Cohort Analysis of the Sabah Population
• OHVIRA syndrome: clinical implications of a delayed diagnosis
• OHVIRA-syndrome (Obstructed hemivagina with ipsilateral renal anomaly) as differential diagnosis of acute lower abdominal pain
• Palliative Care for Pediatric Urology
• Patient with Herlyn-Werner-Wunderlich syndrome and endometriosis achieves successful full-term pregnancy (40 weeks and 6 days): a case report
• Pediatric primary renal lymphoma presenting with multiple masses: A challenging case report and narrative review
• Penile Agenesis Associated with Anorectal Malformation and Bilateral Renal Agenesis: A Case Report and a Review of the Literature
• Pleural-based giant solitary fibrous tumour with associated hypoglycaemia: unusual presentation with pulmonary hypertension in a patient with Doege-Potter syndrome
• Pleural-based giant solitary fibrous tumour with associated hypoglycaemia: unusual presentation with pulmonary hypertension in a patient with Doege-Potter syndrome
• Population-based surveillance of congenital anomalies over 40 years (1981-2020): Results from the Paris Registry of Congenital Malformations (remaPAR)
• Potter Syndrome
• Potter Syndrome
• Pre-pregnancy exposure to arsenic in diet and non-cardiac birth defects
• Pregnancy Outcomes in Patients with Obstructed Hemivagina Ipsilateral Renal Agenesis
• 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 congenital anomalies and prenatal diagnosis by birth institution (public vs. non-public): indicators of inequality in access to elective termination of pregnancy for fetal anomalies
• Recurrent Paravaginal Abscess: An Unusual Presentation of a Distal Ectopic Ureteral Remnant
• Renal agenesis: A meta-analysis of its prevalence and clinical characteristics based on 15 641 184 patients
• Renal Hypodysplasia/Aplasia 3 Caused by a Rare Variant of GREB1L With Incomplete Penetrance in a Chinese Family
• Sirenomelia- A rare congenital anomaly: Case report
• Sirenomelia, renal agenesis and normal amniotic fluid volume
• Sirenomelia: An anatomical assessment and genetic sex determination of two cases
• Solitary fibrous tumor of the liver with Doege-Potter syndrome: An exceptional finding. Discovering the role of blood glucose levels and insulin growth factor II
• Solitary mediastinal fibrous tumor complicated by hypoglycemic crises (Doege-Potter syndrome)
• Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report
• Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report
• Survey of Neonatal Management After Amnioinfusion for Anhydramnios
• Targeted next-generation sequencing in a large series of fetuses with severe renal diseases
• 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
• The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation
• The genetic etiologies of bilateral renal agenesis
• The Outcome of Multicystic Dysplastic Kidney Disease Patients at King Abdulaziz Medical City in Riyadh
• Transfixing Anterior Laryngeal Cleft in a Malformed Stillborn at Term: Case Report
• Treatment of Doege-Potter Syndrome by Bland Transarterial Embolization of a Large Hepatic Solitary Fibrous Tumor
• Trends in Termination of Pregnancy for Foetal Urological Abnormalities in England and Wales: a Cross-Sectional Study
• Uncovering risk factors for kidney injury in children with a solitary functioning kidney
• Unilateral macrocystic dysplasia and contralateral agenesis in a monoamniotic twin
• Unilateral scrotal discomfort in a patient with known renal agenesis: do not forget about Zinner syndrome
• Unique Medley of Cardinal Veins: Duplicated Superior and Inferior Venae Cavae With Left Renal Agenesis and Hemiazygos Continuation of Left Inferior Vena Cava With Drainage Into Left Atrium
• Unraveling the Link Between Fibromuscular Dysplasia and Acute Coronary Syndrome: A Comprehensive Case Report and Analysis
• Vaginoscopic Management of OHVIRA (Obstructive Hemivagina and Ipsilateral Renal Agenesis)
• Vaginoscopic Resection of Oblique Vaginal Septum in OHVIRA Syndrome Before Menarche
• Venous Ulcer in a 5-Year-Old Girl
• Whole exome sequencing reveals two novel mutations in GREB1L in two Chinese families with renal agenesis