 | Up a level |
2020
Lenders, Malte, Nordbeck, Peter 
ORCID: 0000-0002-2560-4068, Kurschat, Christine, Karabul, Nesrin, Kaufeld, Jessica, Hennermann, Julia B., Patten, Monica, Cybulla, Markus, Muentze, Jonas, Ueceyler, Nurcan, Liu, Dan, Das, Anibh M., Sommer, Claudia, Pogoda, Christian, Reiermann, Stefanie, Duning, Thomas, Gaedeke, Jens, Stumpfe, Katharina, Blaschke, Daniela, Brand, Stefan-Martin, Mann, W. Alexander, Kampmann, Christoph, Muschol, Nicole, Canaan-Kuehl, Sima and Brand, Eva
(2020).
Treatment of Fabry's Disease With Migalastat: Outcome From a Prospective Observational Multicenter Study (FAMOUS).
Clin. Pharmacol. Ther., 108 (2).
S. 326 - 338.
HOBOKEN:
WILEY.
ISSN 1532-6535
2016
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
2011
Sullivan, Maren, Rybicki, Lisa A., Winter, Aurelia, Hoffmann, Michael M., Reiermann, Stefanie, Linke, Hannah, Arbeiter, Klaus, Patzer, Ludwig, Budde, Klemens ORCID: 0000-0002-7929-5942, Hoppe, Bernd, Zeier, Martin, Lhotta, Karl, Bock, Andreas, Wiech, Thorsten ORCID: 0000-0003-4053-1474, Gaspert, Ariana, Fehr, Thomas, Woznowski, Magdalena, Berisha, Gani, Malinoc, Angelica, Goek, Oemer-Necmi, Eng, Charis ORCID: 0000-0002-3693-5145 and Neumann, Hartmut P. H.
(2011).
Age-Related Penetrance of Hereditary Atypical Hemolytic Uremic Syndrome.
Ann. Hum. Genet., 75.
S. 639 - 648.
HOBOKEN:
WILEY.
ISSN 1469-1809