Weixun Zhou

ORCID: 0000-0002-7459-7343 · 2 papers in corpus
other 2024
Orphanet journal of rare diseases ·doi:10.1186/s13023-024-03177-y

BACKGROUND AND AIMS: Chronic enteropathy associated with SLCO2A1 gene is a rare intestinal disease caused by loss-of-function SLCO2A1 mutations, with clinical and genetic characteristics remaining largely unknown, especially in Chinese pati…

case-report 2018
BMC cancer ·doi:10.1186/s12885-018-4797-4

BACKGROUND: Endometriosis is a relatively common condition in women of reproductive age. Malignant transformation of intestinal endometriosis is a very rare event. We report a case in which a patient with a history of endometriosis underwen…