A5021149026- Urological Disorders and Treatments
- Congenital Heart Disease Studies
- Pediatric Urology and Nephrology Studies
- Bladder and Urothelial Cancer Treatments
- Urinary Bladder and Prostate Research
- Cardiac Structural Anomalies and Repair
- Mechanical Circulatory Support Devices
- Transplantation: Methods and Outcomes
- Tissue Engineering and Regenerative Medicine
- Urologic and reproductive health conditions
- Ureteral procedures and complications
- Tracheal and airway disorders
- Congenital heart defects research
- Cardiac Valve Diseases and Treatments
- Renal Transplantation Outcomes and Treatments
- Congenital Diaphragmatic Hernia Studies
- Urinary and Genital Oncology Studies
- Aortic Disease and Treatment Approaches
- Cardiac Arrest and Resuscitation
- Pelvic floor disorders treatments
- Cardiovascular Issues in Pregnancy
- Congenital Anomalies and Fetal Surgery
- Cardiomyopathy and Myosin Studies
- Cancer Genomics and Diagnostics
- Coronary Artery Anomalies
VA Greater Los Angeles Healthcare System
2017-2025
Geriatric Research Education and Clinical Center
2023-2025
Children's Hospital of Wisconsin
2015-2024
Medical College of Wisconsin
2015-2024
The University of Western Australia
2022-2024
Dell Children's Medical Center of Central Texas
2024
The University of Texas at Austin
2024
Evidence (Italy)
2023
Michigan Department of Education
2023
American Urological Association
2023
Cecoileal reservoirs were created in 29 patients. Tunneled ureteral implantations along the tenia of cecum provided antireflux mechanism. Plication or tapering terminal ileal segment with ileocecal valve continence The tubular configuration was disrupted either an sigmoid patch, it re-configured a Heineke-Mikulicz type closure to avoid bolus (unit) contractions. Short-term followup examination excretory urography showed no upper tract obstruction. X-rays pouch reflux and interviews revealed...
ABSTRACT Objective To develop a novel prenatal assay based on selective analysis of cell‐free DNA in maternal blood for evaluation fetal Trisomy 21 (T21) and 18 (T18). Methods Two hundred ninety‐eight pregnancies, including 39 T21 seven T18 confirmed aneuploidies, were analyzed using novel, highly multiplexed assay, termed digital selected regions (DANSR™). Cell‐free from samples was DANSR assays loci chromosomes 18. Products 96 separate patients pooled sequenced together. A standard Z ‐test...
No AccessJournal of Urology1 Nov 1988Gastrocystoplasty: An Alternative Solution to the Problem Urological Reconstruction in Severely Compromised Patient Mark C. Adams, Michael E. Mitchell, and Richard Rink AdamsMark Adams More articles by this author , MitchellMichael Mitchell RinkRichard View All Author Informationhttps://doi.org/10.1016/S0022-5347(17)41986-0AboutPDF ToolsAdd favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail isolated segment...
We report a new technique for epispadias repair, which relies on the unique blood supply of corpus cavernosum and glans. The epispadiac phallus is completely disassembled into 3 discrete components: urethral plate, right left hemicorporeal glandular bodies.Ten boys 10 months to 17 years old presented repair between 1990 1994 (6 primary 4 secondary repair). One patient underwent bladder exstrophy closure at time surgery. Two patients prior para-exstrophy flap procedures neither had...
No AccessJournal of UrologyAugmentation1 Aug 1993The Syndrome Dysuria and Hematuria in Pediatric Urinary Reconstruction with Stomach Donald H. Nguyen, Martin A. Bain, Kathy L. Salmonson, George S. Ganesan, Mark W. Burns, Michael E. Mitchell NguyenDonald Nguyen Current address: Division Urology, Children’s Hospital East Tennessee, Medical Office Bldg., Suite 410, 2100 Clinch Ave., Knoxxville, Tennessee 37916. More articles by this author , BainMartin Bain SalmonsonKathy Salmonson...
No AccessJournal of UrologyPediatric Articles1 Sep 1987Intestinocystoplasty and Total Bladder Replacement in Children Young Adults: Followup 129 Cases Michael E. Mitchell Joel A. Piser MitchellMichael PiserJoel View All Author Informationhttps://doi.org/10.1016/S0022-5347(17)43264-2AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail A review consecutive young patients (average age 13.4 years) who underwent intestinocystoplasty...
Stress urinary incontinence in the male patient has been successfully treated with artificial sphincter. However, approximately 15% of patients are still significantly wet despite some improvement this device. These usually almost totally incontinent before sphincter implantation. Of 15 such 80% were rendered satisfactorily dry by adding a second cuff around bulbous urethra. This double technique increases success rate AMS800 to greater than 95%.
No AccessJournal of Urology1 Dec 1993The Mitrofanoff Principle in Urinary Reconstruction Joel M. Sumfest, Mark W. Burns, and Michael E. Mitchell SumfestJoel Sumfest , BurnsMark Burns MitchellMichael View All Author Informationhttps://doi.org/10.1016/S0022-5347(17)35921-9AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail We report the use principle achieve urinary continence 47 patients. A catheterizable channel can be used as...
The clinical significance of copy number variants (CNVs) in congenital heart disease (CHD) continues to be a challenge. Although CNVs including genes can confer risk, relationships between gene dosage and phenotype are still being defined. Our goal was perform quantitative analysis involving 100 well-defined CHD risk identified through previously published human association studies subjects with anatomically defined cardiac malformations. A novel analytical approach permitting CNV frequency...
Hypoplastic left heart syndrome (HLHS) is a clinically and anatomically severe form of congenital disease (CHD). Although prior studies suggest that HLHS has complex genetic inheritance, its etiology remains largely unknown. The goal this study was to characterize risk gene in effect on outcome. We performed next-generation sequencing multigenerational family with high prevalence CHD/HLHS, identifying rare variant the α-myosin heavy chain ( MYH6) gene. A case-control 190 unrelated subjects...