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Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family
Journal of Endocrinological Investigation, 2019 Y. Jiang, J. Du, Y-W Song, W-B Wang, Q. Pang, M. Li, O. Wang, X. Lian, X. Xing, W. Xia +9 moresemanticscholar +1 more sourceImpaired bone microarchitecture in distal interphalangeal joints in patients with primary hypertrophic osteoarthropathy assessed by high-resolution peripheral quantitative computed tomography
Osteoporosis International, 2019 Q. Pang, Q. Pang, Yuping Xu, Yuping Xu, Xuan Qi, L. Huang, V. Hung, J. Xu, R. Liao, Yanfang Hou, Yan Jiang, Wei Yu, O. Wang, Mengtao Li, X. Xing, W. Xia, L. Qin +16 moresemanticscholar +1 more sourceIdentification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study.
Bone, 2018 Yanfang Hou, Yuan-yuan Lin, Xuan Qi, Lu Yuan, R. Liao, Q. Pang, L. Cui, Yan Jiang, O. Wang, Mei Li, Jin Dong, W. Xia +11 moresemanticscholar +1 more source