Results 81 to 90 of about 509 (131)

Endocrine Alterations in Patients With Pachydermoperiostosis. [PDF]

open access: yesJ Clin Endocrinol Metab
Stelmachowska-Banaś M   +21 more
europepmc   +1 more source

Structural basis for prostaglandin and drug transport via SLCO2A1. [PDF]

open access: yesNat Commun
Joshi C   +10 more
europepmc   +1 more source

Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis. [PDF]

open access: yesIntern Med, 2020
Tsuzuki Y   +13 more
europepmc   +1 more source

Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review. [PDF]

open access: yesCureus
Mohammad M   +6 more
europepmc   +1 more source

Primary hypertrophic osteoarthropathy: phenotypic variability and penetrance rate in heterozygotes for <i>SLCO2A1</i> variants. [PDF]

open access: yesJBMR Plus
Arcanjo AM   +6 more
europepmc   +1 more source

“Ulcere genetiche” come rara causa di sanguinamento gastrointestinale occulto oscuro

open access: yes
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]

open access: yesIntest Res
Takeuchi I   +12 more
europepmc   +1 more source

Monogenic forms of inflammatory bowel disease: Genetic mechanisms, models, and clinical implications. [PDF]

open access: yesMol Med
Ghorbanpour A   +5 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy