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Journal Abstract Search

220 related items for PubMed ID: 24012041

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  • 7. A novel homozygous mutation in the SLCO2A1 gene causing pachydermoperiostosis: Efficacy of hydroxychloroquine treatment.
    Alessandrella A, Della Casa R, Alessio M, Puente Prieto J, Strisciuglio P, Melis D.
    Am J Med Genet A; 2018 May; 176(5):1253-1257. PubMed ID: 29681086
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  • 9. Eicosanoid profiling in patients with complete form of pachydermoperiostosis carrying SLCO2A1 mutations.
    Oiwa T, Ishibashi M, Okuno T, Ohba M, Endo Y, Uozumi R, Ghazawi FM, Yoshida K, Niizeki H, Yokomizo T, Nomura T, Kabashima K.
    J Dermatol; 2021 Sep; 48(9):1442-1446. PubMed ID: 34114674
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  • 16. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study.
    Hou Y, Lin Y, Qi X, Yuan L, Liao R, Pang Q, Cui L, Jiang Y, Wang O, Li M, Dong J, Xia W.
    Bone; 2018 Jan; 106():96-102. PubMed ID: 28963081
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  • 17. Primary hypertrophic osteoarthropathy due to a novel SLCO2A1 mutation masquerading as acromegaly.
    Mangupli R, Daly AF, Cuauro E, Camperos P, Krivoy J, Beckers A.
    Endocrinol Diabetes Metab Case Rep; 2017 Jan; 2017():. PubMed ID: 28469926
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  • 18. The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.
    Niizeki H, Shiohama A, Sasaki T, Seki A, Kabashima K, Otsuka A, Kosaki K, Ogo A, Yamada T, Miyasaka M, Matsuoka K, Hirakiyama A, Okuyama T, Matsuda M, Nakabayashi K, Tanese K, Ishiko A, Amagai M, Kudoh J.
    J Dermatol Sci; 2014 Sep; 75(3):193-5. PubMed ID: 24929850
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  • 20. Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice-site mutation in the SLCO2A1 gene.
    Li Z, Yang Q, Yang Y, Wang D, Wang S.
    Br J Dermatol; 2019 Mar; 180(3):682-684. PubMed ID: 26875533
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