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Journal Abstract Search

270 related items for PubMed ID: 31203270

  • 21. [Progress in genetic research on pachydermoperiostosis].
    Du R, Fan L, Huang H, Xiang R.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):105-7. PubMed ID: 26829746
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  • 22. Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterization.
    Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL.
    J Clin Endocrinol Metab; 2013 May; 98(5):E923-33. PubMed ID: 23509104
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  • 24. Clinical and biochemical characteristics of 12 Chinese primary hypertrophic osteoarthropathy patients with HPGD mutations.
    Lu Q, Xu Y, Li S, Zhang Z, Sheng J, Zhang Z.
    Int J Biol Sci; 2022 May; 18(9):3908-3917. PubMed ID: 35813463
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  • 25. 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 May; 2017():. PubMed ID: 28469926
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  • 26. Complete form of pachydermoperiostosis with cutis verticis gyrata resulting from the SLCO2A1 gene mutation.
    Li X, Hao D, Li-Ling J, Jiang X.
    Indian J Dermatol Venereol Leprol; 2019 May; 85(6):681. PubMed ID: 30880718
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  • 27. Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1.
    Ishizuka T, Fujioka K, Mori I, Takeda T, Fuwa M, Ikeda T, Taguchi K, Morita H, Nakabayashi K, Niizeki H.
    Mod Rheumatol Case Rep; 2021 Jul; 5(2):404-408. PubMed ID: 33308032
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  • 29. Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn's disease.
    Umeno J, Esaki M, Hirano A, Fuyuno Y, Ohmiya N, Yasukawa S, Hirai F, Kochi S, Kurahara K, Yanai S, Uchida K, Hosomi S, Watanabe K, Hosoe N, Ogata H, Hisamatsu T, Nagayama M, Yamamoto H, Abukawa D, Kakuta F, Onodera K, Matsui T, Hibi T, Yao T, Kitazono T, Matsumoto T, CEAS study group.
    J Gastroenterol; 2018 Aug; 53(8):907-915. PubMed ID: 29313109
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  • 30. Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.
    Zhang Z, Xia W, He J, Zhang Z, Ke Y, Yue H, Wang C, Zhang H, Gu J, Hu W, Fu W, Hu Y, Li M, Liu Y.
    Am J Hum Genet; 2012 Jan 13; 90(1):125-32. PubMed ID: 22197487
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  • 35. HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing.
    Seifert W, Beninde J, Hoffmann K, Lindner TH, Bassir C, Aksu F, Hübner C, Verbeek NE, Mundlos S, Horn D.
    Eur J Hum Genet; 2009 Dec 13; 17(12):1570-6. PubMed ID: 19568269
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  • 36. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.
    Sasaki T, Niizeki H, Shimizu A, Shiohama A, Hirakiyama A, Okuyama T, Seki A, Kabashima K, Otsuka A, Ishiko A, Tanese K, Miyakawa S, Sakabe J, Kuwahara M, Amagai M, Okano H, Suematsu M, Kudoh J.
    J Dermatol Sci; 2012 Oct 13; 68(1):36-44. PubMed ID: 22906430
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  • 37. Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients.
    Villarreal-Martínez A, Vázquez-Martínez OT, Martínez-de-Villarreal LE, Garay-Mendoza D, Rodríguez-Vivian C, Ocampo-Candiani J, De La Rosa-Marbán E, Ibarra-Ramírez M.
    Indian J Dermatol Venereol Leprol; 2018 Oct 13; 84(4):446-447. PubMed ID: 29770782
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  • 40. Targeted exome sequencing identified a novel mutation hotspot and a deletion in Chinese primary hypertrophic osteoarthropathy patients.
    Chen Y, Li G, Xu Y, Yu T, Zhang Y, Li N, Yao RE, Zhou Y, Wang X, Shen Y, Yin L, Wang J.
    Clin Chim Acta; 2018 Dec 13; 487():264-269. PubMed ID: 30292630
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