Results 71 to 80 of about 509 (131)

A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly. [PDF]

Bone Rep, 2023
Nakano Y, Ohata Y, Fujiwara M, Kubota T, Miyoshi Y, Ozono K.   +5 more
europepmc   +1 more source

Chronic Enteropathy Associated with Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) with Positive Immunohistochemistry for SLCO2A1 Protein. [PDF]

Intern Med, 2022
Ariake C, Hosoe N, Sakurai H, Tojo A, Hayashi Y, Jl Limpias Kamiya K, Sujino T, Takabayashi K, Kosaki K, Seki S, Hisamatsu T, Ogata H, Kanai T.   +12 more
europepmc   +1 more source

What is the appropriate treatment strategy for cryptogenic multifocal ulcerative stenosing enteritis? A single-center experience from China. [PDF]

Front Med (Lausanne), 2022
Yan P, Li K, Cao Y, Wu D, Li J, Qian J, Zhou W, Li J.   +7 more
europepmc   +1 more source

Homozygous Missense Variant in the Solute Carrier Organic Anion Transporter 2A1 (SLCO2A1) Gene Underlies Isolated Nail Clubbing. [PDF]

Genes (Basel), 2023
Umair M, Bilal M, Shah K, Said G, Ahmad F.   +4 more
europepmc   +1 more source

[Imaging Techniques and Differential Diagnosis for Inflammatory Bowel Disease]. [PDF]

J Korean Soc Radiol, 2023
Song KD.
europepmc   +1 more source

SLCO2A1 gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy. [PDF]

J Orthop Translat, 2021
Umeno J, Matsumoto T, Fuyuno Y, Esaki M, Torisu T.   +4 more
europepmc   +1 more source

Is There a Reliable, Rapid, and Economic Diagnostic Approach for SLCO2A1-Related Chronic Enteropathy? [PDF]

J Clin Med
Liu R, Fu Y, Mao J, Jiang Z, Cao Q, Ye L.   +5 more
europepmc   +1 more source

Cryptogenic multifocal ulcerative stenosing enteritis (CMUSE): a rare case and a review of the literature. [PDF]

J Surg Case Rep
Hudson L, Grayson N, Toomey D.
europepmc   +1 more source

Comprehensive evaluation of clinical phenotypes and pathogenic features in late-onset monogenic inflammatory bowel disease: a comparative study with infantile-onset cases. [PDF]

BMC Gastroenterol
Liu H, Shen Y, Xu J, Huang S, Qin T, Zhou Q, Liao J, Xiao F.   +7 more
europepmc   +1 more source

A novel mutation in the SLCO2A1 gene presenting as persistent hypoproteinaemia and refractory iron deficiency anaemia due to chronic enteropathy: a case report. [PDF]

BMC Pediatr
Mettananda S, Bandara P, Rajeindran M, Padeniya P.   +3 more
europepmc   +1 more source