検索結果 - Gopalakrishnan Venkat‐Raman

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  1. 1
    Collagen (<i>COL4A</i>) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis

    Collagen (<i>COL4A</i>) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis 著者: Christine Gast, Reuben J. Pengelly, Matthew Lyon, David J. Bunyan, Eleanor G. Seaby, Nikki Graham, Gopalakrishnan Venkat‐Raman, Sarah Ennis

    出版事項 2015
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    Artigo
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  2. 2
    Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome

    Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome 著者: Petr Vyleťal, Martina Kublová, Marie Hubálek Kalbáčová, Kateřina Hodaňová, Veronika Barešová, Blanka Stibůrková, Jakub Sikora, Helena Hůlková, J Živný, Jacek Majewski, Anne Simmonds, J. P. Fryns, Gopalakrishnan Venkat‐Raman, M. Elleder, Stanislav Kmoch

    出版事項 2006
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    Artigo
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  3. 3
    Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease

    Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease 著者: Christine Gast, Anthony M. Marinaki, Monica Arenas-Hernandez, Sara Campbell, Eleanor G. Seaby, Reuben J. Pengelly, Daniel P. Gale, Thomas M. Connor, David J. Bunyan, Kateřina Hodaňová, Martina Živná, Stanislav Kmoch, Sarah Ennis, Gopalakrishnan Venkat‐Raman

    出版事項 2018
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    Artigo
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  4. 4
    New primary renal diagnosis codes for the ERA-EDTA

    New primary renal diagnosis codes for the ERA-EDTA 著者: Gopalakrishnan Venkat‐Raman, Charles Tomson, Yongsheng Gao, Ronald Cornet, Bénédicte Stengel, Carola Grönhagen‐Riska, C. P. P. Reid, Christian Jacquelinet, Elke Schäeffner, E. W. Boeschoten, Francesco Gaetano Casino, Frédéric Collart, Johan De Meester, Óscar Zurriaga, Reinhard Kramar, Kitty J. Jager, Keith Simpson

    出版事項 2012
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    Artigo
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