Disease: Wilms tumor and pseudohermaphroditism
- 46-XY Denys-Drash Syndrome. Is There a Role for Nephron-sparing Modalities in Management of Renal Masses? A Report of 2 Cases
- 50 Years Ago in TheJournal ofPediatrics: Fifty Years from Syndrome to Gene
- 50 Years Ago in TheJournalofPediatrics: Denys-Drash Syndrome links developmental biology to oncogenesis
- A 3-year-old with a renal mass and large cystic bladder mass
- A case of Potter sequence with WT1 mutation
- A cross-sectional nationwide survey of congenital and infantile nephrotic syndrome in Japan
- A familial WT1 mutation associated with incomplete Denys-Drash syndrome
- A novel WT1 gene mutation in a chinese girl with denys-drash syndrome
- A patient with Denys-Drash syndrome(DDS) underwent renal allotransplantation with preserved autologous kidney
- A review of the genetic background in complicated WT1-related disorders
- An unusual presentation of Denys-Drash syndrome due to bigenic disease
- Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation
- Atypical severe early-onset nephrotic syndrome: Answers
- Bilateral Wilms' tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region
- Bilateral Wilms' tumors in an infant with Denys-Drash syndrome and rarely seen truncation mutation in the WT1 gene-exon 6
- Cancer treatment in disabled children
- Case Report: Denys-Drash Syndrome With <em>WT1</em> Causative Variant Presenting as Atypical Hemolytic Uremic Syndrome
- Case Report: Denys-Drash Syndrome With WT1 Causative Variant Presenting as Atypical Hemolytic Uremic Syndrome
- Characteristics of Nephroblastoma/Nephroblastomatosis in Children with a Clinically Reported Underlying Malformation or Cancer Predisposition Syndrome
- Clinical and pathological features and mutational types of WT1 mutation-associated nephropathy
- Clinical Aspects of WT1 and the Kidney
- Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome
- Congenital diaphragmatic eventration with pulmonary dysplasia in Frasier syndrome due to a WT1 mutation of c.1432+5(IVS9)G>A
- Congenital diaphragmatic eventration with pulmonary dysplasia in Frasier syndrome due to a WT1 mutation of c.1432+5(IVS9)G>A
- Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers
- De novo inflammatory bowel disease in children after solid organ transplantation
- Denys-Drash syndrome associated WT1 glutamine 369 mutants have altered sequence-preferences and altered responses to epigenetic modifications
- Denys-Drash syndrome, septated vagina and low level of anti-Mullerian hormone in male neonate
- Detailed clinical manifestations at onset and prognosis of neonatal-onset Denys-Drash syndrome and congenital nephrotic syndrome of the Finnish type
- Diagnosis of congenital and infantile nephrotic syndromes in renal biopsies in Minas Gerais, Brazil: Six case reports
- Different clinical presentations of WT1 gene mutations
- Discordant phenotypes in monozygotic twins with identical de novo WT1 mutation
- Disorders of sex development 46 XY and bilateral metachronous wilms tumor in a child with mutation in exon 7 of WT1 gene
- Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort
- Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomy
- Effects of WT1 gene downregulation on apoptosis in porcine fetal fibroblasts
- Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysis
- Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome
- Frasier Syndrome: A Rare Cause of Refractory Steroid-Resistant Nephrotic Syndrome
- Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome
- Genetic Testing Proves Crucial in Case of Ambiguous Genitalia and Renal Masses
- Genotype-phenotype correlation of <em>WT1</em> mutation-related nephropathy in Chinese children
- Glomerular epithelial cell phenotype in diffuse mesangial sclerosis: a report of 2 cases with markedly increased urinary podocyte excretion
- Gonadal tumor in Frasier syndrome: a review and classification
- Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report
- Heterogeneity of human WT1 gene
- Immune expression in children with Wilms tumor: a pilot study
- Leukodystrophy with disorders of sex development due to WT1 mutations
- Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant
- Long-term outcome in a case series of Denys-Drash syndrome
- Long-term outcome in pediatric renal tumor survivors: experience of a single center
- Malformation syndromes associated with disorders of sex development
- Malformations, genetic abnormalities, and Wilms tumor
- Management and outcomes in massive bilateral Wilms' tumors
- Management of Bilateral Wilms Tumours
- Management of bilateral Wilms tumours
- Management of bilateral Wilms tumours
- Management of Denys-Drash syndrome: A case series based on an international survey
- Many faces of Wilms Tumor: Recent advances and future directions
- Modulation of VEGF-A Alternative Splicing as a Novel Treatment in Chronic Kidney Disease
- Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome
- New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report
- Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit
- Papers presented at the fall 2020 Pediatric Urologic Oncology Work Group of the Societies of Pediatric Urology meetingNeonatal Serum Electrolyte and Proteinuria Screening on 46,XY Ambiguous Genitalia Patients May Allow Early Diagnosis of Denys-Drash Syndr
- Patients with different or identical genotypes of the WT1 gene present different phenotypes
- Podocytes degrade endocytosed albumin primarily in lysosomes
- Presence of Germ Cells in Disorders of Sex Development: Implications for Fertility Potential and Preservation
- Prophylactic bilateral nephrectomy and preemptive kidney transplantation for Denys-Drash syndrome prior to development of kidney failure
- Recognition mechanism of Wilms' tumour suppressor protein and DNA triplets: insights from molecular dynamics simulation and free energy analysis
- Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome
- Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome
- Refractory Hypertension in Infantile-Onset Denys-Drash Syndrome
- Renal failure from birth-AKI or CKD? Answers
- Repression of CMIP transcription by WT1 is relevant to podocyte health
- Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group
- Risk factors for post-nephrectomy hypotension in pediatric patients
- Role for first zinc finger of WT1 in DNA sequence specificity: Denys-Drash syndrome-associated WT1 mutant in ZF1 enhances affinity for a subset of WT1 binding sites
- Severe hypertriglyceridemia in an infant on chronic hemodialysis
- Single-cell transcriptomes of kidneys in a 6-month-old boy with Denys-Drash syndrome reveal stromal cell heterogeneity in the tumor microenvironment
- Successful treatment of severe ABO antibody-mediated rejection using bortezomib: a case report
- Synchronous Bilateral Wilms Tumor: Five-Year Single-Center Experience with Assessment of Quality of Life
- Syndromic Wilms tumor: a review of predisposing conditions, surveillance and treatment
- Testicular Preservation in 46 XY Denys-Drash Syndrome: A Report of Two Cases
- The Case | Posttransplant upper limb inflammatory nodules
- The role of pre- and postnatal investigations in suspected isolated hypospadias
- The World's Youngest Cadaveric Kidney Transplant: Medical, Surgical and Ethical Issues
- Tumor predisposition syndromes and nephroblastoma : Early diagnosis with imaging
- Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Wilms Tumor Gene 1: Lessons from Kidney Development and Cancer
- Wilms tumor: an update
- Wilms' tumor gene 1: lessons from the interface between kidney development and cancer
- Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome
- WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review
- WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report
- WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia
- WT1 Gene Mutation, p.R462W, in a 46,XY DSD Patient from Egypt with Gonadoblastoma and Review of the Literature
- WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome
- WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease
- WT1-related disorders: more than Denys-Drash syndrome