Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes.
Abell, K; Tolusso, L; Smith, N; Hopkin, R; Vawter-Lee, M; Habli, M; Riddle, S; Calvo-Garcia, MA; Guan, Q; Bierbrauer, K; et al.
Birth Defects Research.
2020;
112:1733-1737.
Contemporary Outcomes of Patients with Isolated Bilateral Renal Agenesis with and without Fetal Intervention.
Riddle, S; Habli, M; Tabbah, S; Lim, FY; Minges, M; Kingma, P; Polzin, W.
Fetal Diagnosis and Therapy: clinical advances and basic research.
2020;
47:675-681.
Complex Fetal Care Case: Amniotic Fluid Replacement in Severe Bladder Outlet Obstruction.
Riddle, S; Tabbah, S; McKinney, D; Kingma, P.
NeoReviews.org.
2020;
21:e425-e430.
Fetoscopic myelomeningocele repair.
Riddle, S; Peiro, JL; Lim, FY; Kingma, PS.
NeoReviews.org.
2020;
21:e66-e71.
Emergency department utilization among pediatric spina bifida patients.
Riddle, S; Meinzen-Derr, J; Tabangin, M; Woodward, J; Wiley, S.
Journal of Pediatric Rehabilitation Medicine.
2019;
12:375-381.
Uncovering new physiology in bilateral renal agenesis following amnioinfusion.
Riddle, SL; Polzin, W; Kingma, P.
Case Reports in Perinatal Medicine.
2019;
8.