Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Christoph Wanner"'
Autor:
Michael J. Klag, Yii-Der Ida Chen, Charles N. Rotimi, W. H. Linda Kao, Michael F. Seldin, Christoph Wanner, Alka Malhotra, Jeffrey M. Curtis, Barbara V. Howard, Xiuqing Guo, Sharon G. Adler, Barbara Truitt, Adam M. Smiles, Philip G. Zager, Denyse Thornley-Brown, Winfried März, Matthias Kretzler, Barry I. Freedman, Robert C. Elston, Huateng Huang, Farook Thameem, Man Li, Vallabh O. Shah, William C. Knowler, Ravi Duggirala, Jeffrey R. Schelling, Tennille S. Leak, Mary E. Comeau, Hanna E. Abboud, Christiane Drechsler, Orly F. Kohn, Lyle G. Best, Jerome I. Rotter, Benjamin J. Keller, Madeleine V. Pahl, Rulan S. Parekh, Robert L. Hanson, Jasmin Divers, Michael W. Smith, Michael M. Hoffmann, Robert G. Nelson, Carl D. Langefeld, Marcus G. Pezzolesi, John R. Sedor, Paul L. Kimmel, Eli Ipp, Stephen J. O'Brien, Shelley A. Cole, E. Jennifer Weil, Robert P. Igo, David J. Leehey, Allison Burlock, Susanne B. Nicholas, Cheryl A. Winkler, Rebekah S. Rasooly, Sudha K. Iyengar, Viji Nair, Kent D. Taylor, Donald W. Bowden
Publikováno v:
PLoS Genetics
Iyengar, SK; Sedor, JR; Freedman, BI; Kao, WHL; Kretzler, M; Keller, BJ; et al.(2015). Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND). PLoS Genetics, 11(8). doi: 10.1371/journal.pgen.1005352. UCLA: Retrieved from: http://www.escholarship.org/uc/item/9s22h1zt
PLoS Genetics, Vol 11, Iss 8, p e1005352 (2015)
Iyengar, SK; Sedor, JR; Freedman, BI; Kao, WHL; Kretzler, M; Keller, BJ; et al.(2015). Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND). PLoS Genetics, 11(8). doi: 10.1371/journal.pgen.1005352. UCLA: Retrieved from: http://www.escholarship.org/uc/item/9s22h1zt
PLoS Genetics, Vol 11, Iss 8, p e1005352 (2015)
Diabetic kidney disease (DKD) is the most common etiology of chronic kidney disease (CKD) in the industrialized world and accounts for much of the excess mortality in patients with diabetes mellitus. Approximately 45% of U.S. patients with incident e
Autor:
Frank Breunig, David G. Warnock, Praveen Jeevaratnam, Andreas D. Kistler, Rudolf P. Wüthrich, Derralynn Hughes, Alexander Scherl, Christoph Wanner, Harald Mischak, Justyna Siwy, Andreas L. Serra, William Mullen
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e20534 (2011)
PLoS ONE; Vol 6
PLoS ONE
PloS one
PLoS ONE; Vol 6
PLoS ONE
PloS one
Female patients affected by Fabry disease, an X-linked lysosomal storage disorder, exhibit a wide spectrum of symptoms, which renders diagnosis, and treatment decisions challenging. No diagnostic test, other than sequencing of the alpha-galactosidase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9e7183d9c19f3c7805083cfe0e61a0
https://eprints.gla.ac.uk/53699/1/53699.pdf
https://eprints.gla.ac.uk/53699/1/53699.pdf