Endocrine Alterations in Patients With Pachydermoperiostosis. [PDF]
Stelmachowska-Banaś M +21 more
europepmc +1 more source
Monogenic inflammatory bowel disease: An unfolding enigma. [PDF]
Ghosh U, Samanta A.
europepmc +1 more source
Structural basis for prostaglandin and drug transport via SLCO2A1. [PDF]
Joshi C +10 more
europepmc +1 more source
Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis. [PDF]
Tsuzuki Y +13 more
europepmc +1 more source
Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review. [PDF]
Mohammad M +6 more
europepmc +1 more source
Primary hypertrophic osteoarthropathy: phenotypic variability and penetrance rate in heterozygotes for <i>SLCO2A1</i> variants. [PDF]
Arcanjo AM +6 more
europepmc +1 more source
“Ulcere genetiche” come rara causa di sanguinamento gastrointestinale occulto oscuro
RIASSUNTO ANALITICO L'anemia sideropenica (IDA), la forma di anemia più frequente in età pediatrica, può presentare un'origine gastrointestinale da perdita ematica cronica.
BEDINI, ALICE
core
Asian-Pacific perspectives on the management of very early-onset inflammatory bowel disease. [PDF]
Takeuchi I +12 more
europepmc +1 more source
Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report. [PDF]
Fang Y, Gu W, Luo Y, Chen J.
europepmc +1 more source
Monogenic forms of inflammatory bowel disease: Genetic mechanisms, models, and clinical implications. [PDF]
Ghorbanpour A +5 more
europepmc +1 more source

