 | Up a level |
2017
Lenders, Malte, Hennermann, Julia B., Kurschat, Christine, Rolfs, Arndt, Canaan-Kuehl, Sima, Sommer, Claudia, Ueceyler, Nurcan, Kampmann, Christoph, Karabul, Nesrin, Giese, Anne-Katrin, Duning, Thomas, Stypmann, Joerg, Kraemer, Johannes, Weidemann, Frank, Brand, Stefan-Martin, Wanner, Christoph and Brand, Eva (2017). Treatment and clinical survey of females with Fabry disease in Germany. Mol. Genet. Metab., 120 (1-2). S. S82 - 1. SAN DIEGO: ACADEMIC PRESS INC ELSEVIER SCIENCE. ISSN 1096-7206
Lenders, Malte, Schmitz, Boris 
ORCID: 0000-0001-7041-7424, Stypmann, Joerg, Duning, Thomas, Brand, Stefan-Martin, Kurschat, Christine and Brand, Eva
(2017).
Renal function at ERT-naive baseline predicts long-term outcome in Fabry disease.
Mol. Genet. Metab., 120 (1-2).
S. S82 - 1.
SAN DIEGO:
ACADEMIC PRESS INC ELSEVIER SCIENCE.
ISSN 1096-7206
Lenders, Malte, Schmitz, Boris ORCID: 0000-0001-7041-7424, Stypmann, Joerg, Duning, Thomas, Brand, Stefan-Martin, Kurschat, Christine and Brand, Eva
(2017).
Renal function predicts long-term outcome on enzyme replacement therapy in patients with Fabry disease.
Nephrol. Dial. Transplant., 32 (12).
S. 2090 - 2098.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2385
2016
Lenders, Malte, Hennermann, Julia B., Kurschat, Christine, Rolfs, Arndt, Canaan-Kuehl, Sima, Sommer, Claudia, Ueceyler, Nurcan, Kampmann, Christoph, Karabul, Nesrin, Giese, Anne-Katrin, Duning, Thomas, Stypmann, Joerg, Kraemer, Johannes, Weidemann, Frank, Brand, Stefan-Martin, Wanner, Christoph and Brand, Eva (2016). Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease. Orphanet J. Rare Dis., 11. LONDON: BMC. ISSN 1750-1172
Lenders, Malte, Weidemann, Frank, Kurschat, Christine, Canaan-Kuehl, Sima, Duning, Thomas, Stypmann, Joerg, Schmitz, Boris ORCID: 0000-0001-7041-7424, Reiermann, Stefanie, Kraemer, Johannes, Blaschke, Daniela, Wanner, Christoph, Brand, Stefan-Martin and Brand, Eva
(2016).
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant.
Orphanet J. Rare Dis., 11.
LONDON:
BMC.
ISSN 1750-1172