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Anzahl der Publikationen: 5
Zeitschriftenartikel
Angermann, Susanne; Schier, Johannes; Baumann, Marcus; Steubl, Dominik; Hauser, Christine; Lorenz, Georg; Günthner, Roman; Braunisch, Matthias; Kemmner, Stephan; Satanovskij, Robin; Haller, Bernhard; Heemann, Uwe; Grimmer, Timo; Lehnert, Thomas; Bieber, Richard; Pachmann, Martin; Braun, Jürgen; Scherf, Julia; Schätzle, Gabriele; Fischereder, Michael und Schmaderer, Christoph
(2018):
Cognitive Impairment is Associated with Mortality in Hemodialysis Patients.
In: Journal of Alzheimers Disease
Satanovskij, Robin; Bader, Alhaddad; Block, Matthias; Herbst, Victor; Schlumberger, Wolfgang; Haack, Tobias; Nockher, Wolfgang Andreas; Heemann, Uwe; Renders, Lutz; Schmaderer, Christoph; Angermann, Susanne; Wen, Ming; Meitinger, Thomas; Scherberich, Jürgen und Steubl, Dominik
(2017):
A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations - A tool for the diagnosis of uromodulin-associated kidney disease.
In: Clinical Biochemistry, Bd. 50, Nr. 3: S. 155-158
Steubl, Dominik; Block, Matthias; Herbst, Victor; Nockher, Wolfgang Andreas; Schlumberger, Wolfgang; Satanovskij, Robin; Angermann, Susanne; Hasenau, Anna-Lena; Stecher, Lynne; Heemann, Uwe; Renders, Lutz und Scherberich, Jürgen
(2016):
Plasma Uromodulin Correlates With Kidney Function and Identifies Early Stages in Chronic Kidney Disease Patients.
In: Medicine, Bd. 95, Nr. 10, e3011
[PDF, 393kB]
Kremer, Laura S.; Distelmaier, Felix; Alhaddad, Bader; Hempel, Maja; Iuso, Arcangela; Küpper, Clemens; Mühlhausen, Chris; Kovacs-Nagy, Reka; Satanovskij, Robin; Graf, Elisabeth; Berutti, Riccardo; Eckstein, Gertrud; Durbin, Richard; Sauer, Sascha; Hoffmann, Georg F.; Strom, Tim M.; Santer, René; Meitinger, Thomas; Klopstock, Thomas; Prokisch, Holger und Haack, Tobias B.
(2016):
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy.
In: American Journal of Human Genetics, Bd. 98, Nr. 2: S. 358-362
Kouz, Karim; Lissewski, Christina; Spranger, Stephanie; Mitter, Diana; Riess, Angelika; Lopez-Gonzalez, Vanesa; Lüttgen, Sabine; Aydin, Hatip; Deimling, Florian von; Evers, Christina; Hahn, Andreas; Hempel, Maja; Issa, Ulrike; Kahlert, Anne-Karin; Lieb, Adrian; Villavicencio-Lorini, Pablo; Juliana Ballesta-Martinez, Maria; Nampoothiri, Sheela; Ovens-Raeder, Angela; Puchmajerová, Alena; Satanovskij, Robin; Seidel, Heide; Unkelbach, Stephan; Zabel, Bernhard; Kutsche, Kerstin und Zenker, Martin
(2016):
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation.
In: Genetics in Medicine, Bd. 18, Nr. 12: S. 1226-1234