يعرض 1 - 6 نتائج من 6 نتيجة بحث عن '"Tang, Xia Jing"', وقت الاستعلام: 0.34s تنقيح النتائج
  1. 1
    Comparison of outcomes between overlapping-spot and single-spot photodynamic therapy for circumscribed choroidal hemangioma

    المؤلفون: Su, Zhao-An, Tang, Xia-Jing, Zhang, Li-Xia, Su, Xiao-Hong

    المصدر: International Journal of Ophthalmology, Vol 7, Iss 1, Pp 66-70 (2014)

    مصطلحات موضوعية: photodynamic therapy, lcsh:Ophthalmology, Clinical Research, lcsh:RE1-994, spot pattern, eye diseases, circumscribed choroidal hemangioma

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ff0ed1bcede43c1e91662550126d10f6
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949461/

    View record in OpenAIRE

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  2. 2
    Academic Journal
    Involvement of PI3K/Akt Pathway in TGF-β 2 -Mediated Epithelial Mesenchymal Transition in Human Lens Epithelial Cells

    المؤلفون: Yao, Ke, Ye, Pan Pan, Tan, Jian, Tang, Xia Jing, Shen Tu, Xing Chao

    المصدر: Ophthalmic Research ; volume 40, issue 2, page 69-76 ; ISSN 0030-3747 1423-0259

    الاتاحة: http://dx.doi.org/10.1159/000113884
    https://www.karger.com/Article/Pdf/113884

    View record in BASE

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  3. 3
    Academic Journal
    Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7 gene in a Chinese family with X-linked idiopathic congenital nystagmus.

    المؤلفون: Song, Feng-wei, Chen, Bin-bin, Sun, Zhao-hui, Wu, Li-ping, Zhao, Su-juan, Miao, Qi, Tang, Xia-jing

    المصدر: Journal of Zhejiang University: Science B; Jun2013, Vol. 14 Issue 6, p479-486, 8p

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  4. 4
    Periodical
    Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7gene in a Chinese family with X-linked idiopathic congenital nystagmus

    المؤلفون: Song, Feng-wei, Chen, Bin-bin, Sun, Zhao-hui, Wu, Li-ping, Zhao, Su-juan, Miao, Qi, Tang, Xia-jing

    المصدر: Journal of Zhejiang University - Science B; June 2013, Vol. 14 Issue: 6 p479-486, 8p

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  5. 5
    Academic Journal
    Erratum to: Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7 gene in a Chinese family with X-linked idiopathic congenital nystagmus.

    المؤلفون: Song, Feng-wei, Chen, Bin-bin, Sun, Zhao-hui, Wu, Li-ping, Zhao, Su-juan, Miao, Qi, Tang, Xia-jing

    المصدر: Journal of Zhejiang University: Science B; Sep2013, Vol. 14 Issue 9, p866-866, 1p

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  6. 6
    Periodical
    Erratum to: Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7gene in a Chinese family with X-linked idiopathic congenital nystagmus

    المؤلفون: Song, Feng-wei, Chen, Bin-bin, Sun, Zhao-hui, Wu, Li-ping, Zhao, Su-juan, Miao, Qi, Tang, Xia-jing

    المصدر: Journal of Zhejiang University - Science B; September 2013, Vol. 14 Issue: 9 p866-866, 1p

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