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Journal Abstract Search

270 related items for PubMed ID: 31203270

  • 1. Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Idiopathic Arthritis: A Novel SLCO2A1 Mutation and Imaging Findings.
    Torgutalp M, Durmaz CD, Karabulut HG, Seifert W, Horn D, Akkaya Z, Turgay M.
    Cytogenet Genome Res; 2019; 158(3):126-132. PubMed ID: 31203270
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  • 2. Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing.
    Nicolau R, Beirão T, Guimarães F, Aguiar F, Ganhão S, Rodrigues M, Grangeia A, Brito I.
    Pediatr Rheumatol Online J; 2023 May 24; 21(1):48. PubMed ID: 37226222
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  • 3. Pachydermoperiostosis: The value of molecular diagnosis.
    Seta V, Capri Y, Battistella M, Bagot M, Bourrat E.
    Ann Dermatol Venereol; 2017 Dec 24; 144(12):799-803. PubMed ID: 28916395
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  • 4. 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 24; 106():96-102. PubMed ID: 28963081
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  • 5. Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathy.
    Bloch A, Couture G, Isidor B, Ricquebourg M, Bourrat E, Lipsker D, Taillan B, Combier A, Chiaverini C, Moufle F, Delobel B, Richette P, Collet C.
    Eur J Med Genet; 2023 Feb 24; 66(2):104689. PubMed ID: 36549465
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  • 6. 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 24; 176(5):1253-1257. PubMed ID: 29681086
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  • 7. Two novel mutations in the SLCO2A1 gene in a Chinese patient with primary hypertrophic osteoarthropathy.
    Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL.
    Gene; 2014 Jan 25; 534(2):421-3. PubMed ID: 24185079
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  • 8. Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.
    Lee S, Park SY, Kwon HJ, Lee CH, Kim OH, Rhee Y.
    J Korean Med Sci; 2016 May 25; 31(5):735-42. PubMed ID: 27134495
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  • 9. Pachydermoperiostosis in an African patient caused by a Chinese/Japanese SLCO2A1 mutation-case report and review of literature.
    Madruga Dias JA, Rosa RS, Perpétuo I, Rodrigues AM, Janeiro A, Costa MM, Gaião L, Pereira da Silva JA, Fonseca JE, Miltenberger-Miltenyi G.
    Semin Arthritis Rheum; 2014 Feb 25; 43(4):566-9. PubMed ID: 24012041
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  • 12. Three novel mutations in the SLCO2A1 gene in two Chinese families with primary hypertrophic osteoarthropathy.
    Cheng R, Li M, Guo Y, Yao Y, Gao C, Yao Z.
    Eur J Dermatol; 2013 Feb 25; 23(5):636-9. PubMed ID: 24153155
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  • 13. Pachydermoperiostosis of the complete type: A novel missense mutation c.101T > C in the SLCO2A1 gene.
    Ma W, Guo S, Li Y, Li Z.
    Eur J Med Genet; 2017 Aug 25; 60(8):433-436. PubMed ID: 28602931
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