Park SS

No ORCID on file · 5 papers in corpus · active 2012-2025

Study types

  • case-report 1

Condition tags

  • endometriosis 1
case-report 2025
Recurrent Hemothorax and Hemoperitoneum in Endometriosis: A Case Report
Cureus ·doi:10.7759/cureus.89503

Extra-pelvic endometriosis, defined as the presence of endometrial tissue or stroma outside of the pelvic cavity, is a rare cause of hemothorax and hemoperitoneum. Here, we present a case of a 34-year-old woman with a history of endometrios…

2020
Differences in midazolam premedication effects on recovery after short-duration ambulatory anesthesia with propofol or sevoflurane for gynecologic surgery in young patients: A randomized controlled trial.
Medicine ·doi:10.1097/md.0000000000023194

BackgroundAnxiolytic premedication requires careful consideration owing to potential side effects including delayed recovery after ambulatory anesthesia. We aimed to compare the effect of midazolam on recovery profiles postoperatively, depe…

2017
Identification of Site-specific Recurrence Following Primary Radiation Therapy for Prostate Cancer Using C-11 Choline Positron Emission Tomography/Computed Tomography: A Nomogram for Predicting Extrapelvic Disease.
European urology ·doi:10.1016/j.eururo.2016.08.055

BackgroundManagement of recurrent prostate cancer (CaP) after radiotherapy (RT) is dependent on accurate localization of the site of recurrent disease.ObjectiveTo describe the anatomic patterns and clinical features associated with CaP recu…

2016
Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma.
BMC medical genetics ·doi:10.1186/s12881-016-0306-2

Backgroundvon Hippel-Lindau (VHL) disease is a rare hereditary tumor syndrome caused by VHL gene mutations that is characterized by heterogeneous phenotypes such as benign/malignant tumors of the central nervous system, retina, kidney, adre…

2012
Transcriptome correlation analysis identifies two unique craniosynostosis subtypes associated with IRS1 activation.
Physiological genomics ·doi:10.1152/physiolgenomics.00085.2012

The discovery of causal mechanisms associated with nonsyndromic craniosynostosis has proven to be a difficult task due to the complex nature of the disease. In this study, differential transcriptome correlation analysis was used to identify…