Dr. Stuart Bauer received his medical degree from the University of Rochester School of Medicine in 1968, interned at King County Hospital in Seattle Washington, completed his residency in Urology at Tufts-New England Medical Center in Boston and had an elective with Mr. Richard Turner Warwick at the Middlesex Hospital in London. He moved to Children’s Hospital Boston in 1977 developing the first urodynamics laboratory entirely devoted to children and rose to Professor of Surgery (Urology) at Harvard Medical School in 2000. His research has led to breakthroughs in understanding of bladder function in children with neurologic, anatomic, and functional disorders. His findings in newborns with myelodysplasia led to a paradigm shift in how these babies are currently managed worldwide.
He has published more than 196 articles in peer-reviewed journals, written over 70 chapters in urologic textbooks and edited 2 books on the evaluation and management of children with urologic diseases. In addition, he has been a visiting professor at numerous institutions in the United States and worldwide and given lectures at over 150 scientific meetings, locally, nationally and internationally. From 2008 to 2014, he served as President of the International Children’s Continence Society where he has worked tirelessly to advance the objectives of this global society, namely improvement in the care of children with bladder dysfunction.
He has received a number of awards recognizing his accomplishments during his long and distinguished career: in 2009, he received the Pediatric Urology Progress Medal; in October, 2011 Dr. Bauer was awarded the Pediatric Urology Medal from the Section on Urology of the American Academy of Pediatrics for his outstanding contributions to his field of interest during his career; a Life Time Achievement Medal from the Spina Bifida Association of America was granted to him in March 2012; the American Urologic Association recognized his advances in the care of children with neurogenic bladder dysfunction by presenting him with the Victor A. Politano Award; and, most recently, on September 11, 2021, his research was cited when the American Urological Association Care Foundation honored him with the John W. Duckett Jr., MD Pediatric Urology Research Excellence Award.
Publications
Real-Time Bladder Volume Monitoring for Pediatric Patients Using a Commercially Available Wearable Ultrasound Device. View Abstract
Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62. View Abstract
Sentiments of Individuals with Interstitial Cystitis/Bladder Pain Syndrome Toward Pentosan Polysulfate Sodium: Infodemiology Study. View Abstract
Editorial Comment on "Correlation not Causation-Looking Back at the History of VUR". View Abstract
Expert Consensus on Pediatric Urodynamics Reporting Using Modified Delphi Technique. View Abstract
Intradetrusor botox injection and augmentation cystoplasty trends among spina bifida patients at US freestanding children's hospitals. View Abstract
The impact of clean intermittent catheterization on students and families in the school environment. View Abstract
Facilitators and challenges to transitioning to self-catheterization: Patient and caregiver perspectives. View Abstract
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. View Abstract
The art of introducing clean intermittent catheterization: How families respond and adapt: A qualitative study. View Abstract
Accuracy of contrast-enhanced voiding urosonography using Optison™ for diagnosis of vesicoureteral reflux in children. View Abstract
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract. View Abstract
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract. View Abstract
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. View Abstract
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract. View Abstract
Onabotulinumtoxin A (Botox): A reasonable alternative for refractory neurogenic bladder dysfunction in children and young adults. View Abstract
Low energy availability and impact sport participation as risk factors for urinary incontinence in female athletes. View Abstract
Losartan prevents bladder fibrosis and protects renal function in rat with neurogenic paralysis bladder. View Abstract
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. View Abstract
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT). View Abstract
Anxiety, distress, and pain in pediatric urodynamics. View Abstract
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations. View Abstract
The influence of delay elimination communication on the prevalence of primary nocturnal enuresis-a survey from Mainland China. View Abstract
ICS educational module: Cystometry in children. View Abstract
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. View Abstract
Antibiotic Exposure and Reduced Short Chain Fatty Acid Production after Hematopoietic Stem Cell Transplant. View Abstract
ICS educational module: Pressure flow study in children. View Abstract
Pelvic floor laxity: A not so rare but unrecognized form of daytime urinary incontinence in peripubertal and adolescent girls. View Abstract
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux. View Abstract
The value of synchro-cystourethrometry for evaluating the relationship between urethral instability and overactive bladder. View Abstract
Minor procedure, major impact: Patient-reported outcomes following urethral meatotomy. View Abstract
Diagnosis and management of bladder bowel dysfunction in children with urinary tract infections: a position statement from the International Children's Continence Society. View Abstract
Evaluation and management of tethered cord syndrome in occult spinal dysraphism: Recommendations from the international children's continence society. View Abstract
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling. View Abstract
Establishing a standard protocol for the voiding cystourethrography (VCUG). View Abstract
Establishing a standard protocol for the voiding cystourethrography. View Abstract
The transition of young adults with lifelong urological needs from pediatric to adult services: An international children's continence society position statement. View Abstract
The vexing problem of underactive bladder in children: a viable alternative. View Abstract
Commentary regarding "What is a representative voiding pattern in children with lower urinary tract symptoms? Lack of consistent findings in ambulatory and conventional urodynamics tests". View Abstract
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract. View Abstract
Sacral agenesis and neurogenic bladder: Long-term outcomes of bladder and kidney function. View Abstract
Management of functional nonretentive fecal incontinence in children: Recommendations from the International Children's Continence Society. View Abstract
Treatment of daytime urinary incontinence: A standardization document from the International Children's Continence Society. View Abstract
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development. View Abstract
Validation of a bowel dysfunction instrument for adolescents with spina bifida. View Abstract
International Children's Continence Society standardization report on urodynamic studies of the lower urinary tract in children. View Abstract
Self-cathing experience journal: Enhancing the patient and family experience in clean intermittent catheterization. View Abstract
Urinary incontinence in spina bifida: Initial instrument validation. View Abstract
Semen parameters in adolescents with varicocele: association with testis volume differential and total testis volume. View Abstract
The standardization of terminology of lower urinary tract function in children and adolescents: Update report from the standardization committee of the International Children's Continence Society. View Abstract
Combined cystometrography and electromyography of the external urethral sphincter following complete primary repair of bladder exstrophy. View Abstract
The standardization of terminology of lower urinary tract function in children and adolescents: update report from the Standardization Committee of the International Children's Continence Society. View Abstract
Re: Dannaway J, Ng H, Deshpande AV. Adherence to ICCS nomenclature guidelines in subsequent literature: a bibliometric study. Neurourol Urodyn 2013;32;952-956. View Abstract
Should urodynamics be the basis for classification of lower urinary tract symptoms in children? View Abstract
Management of functional constipation in children with lower urinary tract symptoms: report from the Standardization Committee of the International Children's Continence Society. View Abstract
In utero closure of myelomeningocele does not improve lower urinary tract function. View Abstract
Protective locus against renal scarring on chromosome 11 in affected sib pairs with familial vesicoureteral reflux identified by single nucleotide polymorphism linkage analysis. View Abstract
Erratum to: Practical consensus guidelines for the management of enuresis. View Abstract
International Children's Continence Society's recommendations for initial diagnostic evaluation and follow-up in congenital neuropathic bladder and bowel dysfunction in children. View Abstract
International Children's Continence Society's recommendations for therapeutic intervention in congenital neuropathic bladder and bowel dysfunction in children. View Abstract
Urodynamic findings in patients with Currarino syndrome. View Abstract
The management of adolescents with neurogenic urinary tract and bowel dysfunction. View Abstract
Practical consensus guidelines for the management of enuresis. View Abstract
Adult care of children from pediatric urology. View Abstract
Risk factors of sudden death in young adult patients with myelomeningocele. View Abstract
Genome gender diversity in affected sib-pairs with familial vesico-ureteric reflux identified by single nucleotide polymorphism linkage analysis. View Abstract
Screening for malignancy after augmentation cystoplasty in children with spina bifida: a decision analysis. View Abstract
Urodynamic testing in children: indications, technique, interpretation and significance. View Abstract
Prenatal versus postnatal repair of myelomeningocele. View Abstract
Ultrasound versus computerized tomography for evaluating urolithiasis. View Abstract
A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5. View Abstract
What is the optimal surgical strategy for bulbous urethral stricture in boys? View Abstract
Nomograms for predicting annual resolution rate of primary vesicoureteral reflux: results from 2,462 children. View Abstract
Caliceal diverticula in children: natural history and management. View Abstract
Varicocele surgery: a decade's experience at a children's hospital. View Abstract
Long-term efficacy of artificial urinary sphincters in children. View Abstract
Neurogenic bladder: etiology and assessment. View Abstract
Relationship of varicocele grade and testicular hypotrophy to semen parameters in adolescents. View Abstract
Standardizing terminology in pediatric urology. View Abstract
Bladder and external urethral sphincter function after prenatal closure of myelomeningocele. View Abstract
Safety and durability of dextranomer injections for urinary incontinence. View Abstract
The standardization of terminology of lower urinary tract function in children and adolescents: report from the Standardisation Committee of the International Children's Continence Society. View Abstract
Tissue-engineered autologous bladders for patients needing cystoplasty. View Abstract
Diagnosis and management of dysfunctional voiding. View Abstract
Renal biopsy in congenital ureteropelvic junction obstruction: evidence for parenchymal maldevelopment. View Abstract
Neurogenic bladder dysfunction after sacrococcygeal teratoma resection. View Abstract
Testicular hypotrophy does not correlate with grade of adolescent varicocele. View Abstract
Balanitis xerotica obliterans in boys. View Abstract
Intermittent testicular torsion: diagnostic features and management outcomes. View Abstract
Bladder growth and development after complete primary repair of bladder exstrophy in the newborn with comparison to staged approach. View Abstract
Is adolescent varicocele a progressive disease process? View Abstract
Anterior urethral valves and diverticula in children: a result of ruptured Cowper's duct cyst? View Abstract
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity. View Abstract
Botulinum-A toxin injection into the detrusor: a safe alternative in the treatment of children with myelomeningocele with detrusor hyperreflexia. View Abstract
The management of the myelodysplastic child: a paradigm shift. View Abstract
Mechanisms of failure of endoscopic treatment of vesicoureteral reflux based on endoscopic anatomy. View Abstract
Signaling through PI3K/Akt mediates stretch and PDGF-BB-dependent DNA synthesis in bladder smooth muscle cells. View Abstract
Fibroepithelial polyps causing ureteropelvic junction obstruction in children. View Abstract
Rate and predictors of spontaneous resolution of prenatally diagnosed primary nonrefluxing megaureter. View Abstract
The overactive bladder in childhood: long-term results with conservative management. View Abstract
The effect of surgery for split spinal cord malformation on neurologic and urologic function. View Abstract
The effects and challenges of bladder outlet obstruction. View Abstract
Normal urodynamics in patients with bladder exstrophy: are they achievable? View Abstract
The incidence of intersexuality in children with cryptorchidism and hypospadias: stratification based on gonadal palpability and meatal position. View Abstract
Improved bladder function after prophylactic treatment of the high risk neurogenic bladder in newborns with myelomentingocele. View Abstract
Oxybutynin chloride inhibits proliferation and suppresses gene expression in bladder smooth muscle cells. View Abstract
Urodynamic findings in children with isolated epispadias. View Abstract
Reservoir calculi: a comparison of reservoirs constructed from stomach and other enteric segments. View Abstract
Adverse urologic consequences of spinal cord resection at the time of kyphectomy: value of preoperative urodynamic evaluation. View Abstract
Current findings in diagnostic laparoscopic evaluation of the nonpalpable testis. View Abstract
The challenge of the expanding role of urodynamic studies in the treatment of children with neurological and functional disabilities. View Abstract
Urachal anomalies: defining the best diagnostic modality. View Abstract
A single-system ectopic ureter draining an ectopic dysplastic kidney: delayed diagnosis in the young female with continuous urinary incontinence. View Abstract
Unilateral suprainguinal ectopic scrotum: the role of the gubernaculum in the formation of an ectopic scrotum. View Abstract
Hypoplastic dysplastic kidney with a vaginal ectopic ureter identified by technetium-99m-DMSA scintigraphy. View Abstract
Estimating normal bladder capacity in children. View Abstract
Pressure at residual volume: a useful adjunct to standard fill cystometry. View Abstract
Vesicoureteral reflux in children: incidence and severity in siblings. View Abstract
Correlation of cystographic bladder morphology and neuroanatomy in boys with posterior urethral valves. View Abstract
Continent urinary diversion: the Children's Hospital experience. View Abstract
Late effects of early surgery on lipoma and lipomeningocele in children less than 1 year old. View Abstract
Urodynamic and neurophysiologic evaluation of patients with diastematomyelia. View Abstract
Reconstructive options in genitourinary rhabdomyosarcoma. View Abstract
Natural history of vesicoureteral reflux in siblings. View Abstract
Ten-year experience with the artificial urinary sphincter in children. View Abstract
Bladder stimulation therapy improves bladder compliance: results from a multi-institutional trial. View Abstract
Congenital posterior urethral perineal fistulae: a unique form of urethral duplication. View Abstract
Urinary dysfunction in Duchenne muscular dystrophy. View Abstract
Functional bladder capacity measured during radionuclide cystography in children. View Abstract
Electrophysiological and urodynamic studies to monitor surgical outcome in children with tethered spinal cords. View Abstract
The long-term urological response of neonates with myelodysplasia treated proactively with intermittent catheterization and anticholinergic therapy. View Abstract
Urodynamic findings in children with spinal cord ischemia. View Abstract
The effects of delayed diagnosis and treatment in patients with an occult spinal dysraphism. View Abstract
Retained sacral function in children with high level myelodysplasia. View Abstract
Comparative urodynamics of appendiceal and ureteral Mitrofanoff conduits in children. View Abstract
Spared sacral function in patients with complete thoracolumbar myelodysplasia. View Abstract
Meatal based hypospadias repair with the use of a dorsal subcutaneous flap to prevent urethrocutaneous fistula. View Abstract
Management of severe hypospadias with a 2-stage repair. View Abstract
Abnormal detrusor function precipitating hydronephrosis identified by extended voiding cystometry. View Abstract
The use of intravesical oxybutynin chloride in patients with detrusor hypertonicity and detrusor hyperreflexia. View Abstract
Laparoscopic evaluation of the nonpalpable tests: a prospective assessment of accuracy. View Abstract
The neurosurgical implications of continuous neurourological surveillance of children with myelodysplasia. View Abstract
Urologic management of spinal cord injury in children. View Abstract
The effect of gastric augmentation on bladder function. View Abstract
Continuous urodynamic surveillance of babies with myelodysplasia: implications for further neurosurgery. View Abstract
Urodynamic dysfunction in walking myelodysplastic children. View Abstract
Bladder functional changes resulting from lipomyelomeningocele repair. View Abstract
The prophylactic value of clean intermittent catheterization and anticholinergic medication in newborns and infants with myelodysplasia at risk of developing urinary tract deterioration. View Abstract
The long-term results of artificial sphincters in children. View Abstract
Vesical manifestations of chronic granulomatous disease in children. Its relation to eosinophilic cystitis. View Abstract
Paratesticular rhabdomyosarcoma: results of therapy in 18 cases. View Abstract
The urodynamic consequences of posterior urethral valves. View Abstract
Management of the obstructed urinary tract associated with neurogenic bladder dysfunction. View Abstract
Evaluation and management of urinary incontinence after surgery for posterior urethral valves. View Abstract
Descent of the bladder neck: a urographic finding in denervation of the urethral sphincter in children with myelodysplasia. View Abstract
Modulation of the bulbocavernosus reflex during voiding: loss of inhibition in upper motor neuron lesions. View Abstract
The use of rectus fascia to manage urinary incontinence. View Abstract
The unrecognized neuropathic bladder of infancy. View Abstract
Congenital obstructed megaureters in early infancy: diagnosis and treatment. View Abstract
Clean, intermittent catheterization of infants with neurogenic bladder. View Abstract
Lower pole ureteropelvic junction obstruction and incomplete renal duplication. View Abstract