Hernandez D

No ORCID on file · 2 papers in corpus · active 2026
2026
Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy.
Orphanet journal of rare diseases ·doi:10.1186/s13023-026-04348-9

OBJECTIVE: Autosomal dominant pathogenic variants in WFS1 cause a spectrum of disorders with phenotypic manifestations including low-frequency sensorineural hearing loss, optic nerve atrophy accompanied by low- to mid-frequency sensorineura…

2026
Risk-reducing gynecologic surgery decisions in Lynch syndrome at a safety-net hospital and university medical center.
Gynecologic Oncology ·doi:10.1016/j.ygyno.2026.04.017

ObjectiveTo explore uptake of risk-reducing gynecologic surgery in a diverse patient population with Lynch syndrome.MethodsChart reviews of women with Lynch syndrome were conducted at a safety-net hospital and university medical center, inc…