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- University of Regensburg (6)
- Biology, Preclinical Medicine (6)
- Institut für Physiologie (6)
- Prof. Dr. Richard Warth (6)
- Institut für Physiologie (6)
- Biology, Preclinical Medicine (6)
B
Bandulik, Sascha and Tauber, Philipp and Penton, David and Schweda, Frank and Tegtmeier, Ines and Sterner, Christina and Lalli, Enzo and Lesage, Florian and Hartmann, Michaela and Barhanin, Jacques and Warth, Richard (2013) Severe Hyperaldosteronism in Neonatal Task3 Potassium Channel Knockout Mice Is Associated With Activation of the Intraadrenal Renin-Angiotensin System. ENDOCRINOLOGY, 154 (8). pp. 2712-2722. ISSN 0013-7227
G
Guertler, Florian and Jordan, Katrin and Tegtmeier, Ines and Herold, Janina and Stindl, Julia and Warth, Richard and Bandulik, Sascha (2020) Cellular Pathophysiology of Mutant Voltage-Dependent Ca2+ Channel CACNA1H in Primary Aldosteronism. ENDOCRINOLOGY, 161 (10): bqaa135. ISSN 0013-7227, 1945-7170
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Kuppusamy, Maniselvan and Caroccia, Brasilina and Stindl, Julia and Bandulik, Sascha and Lenzini, Livia and Gioco, Francesca and Fishman, Veniamin and Zanotti, Giuseppe and Gomez-Sanchez, Celso and Bader, Michael and Warth, Richard and Rossi, Gian Paolo (2014) A Novel KCNJ5-insT149 Somatic Mutation Close to, but Outside, the Selectivity Filter Causes Resistant Hypertension by Loss of Selectivity for Potassium. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 99 (9). E1765-E1773. ISSN 0021-972X, 1945-7197
M
Monticone, Silvia and Bandulik, Sascha and Stindl, Julia and Zilbermint, Mihail and Dedov, Ivan and Mulatero, Paolo and Allgaeuer, Michael and Lee, Chyi-Chia Richard and Stratakis, Constantine A. and Williams, Tracy A. and Tiulpakov, Anatoly (2015) A Case of Severe Hyperaldosteronism Caused by a De Novo Mutation Affecting a Critical Salt Bridge Kir3.4 Residue. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 100 (1). E114-E118. ISSN 0021-972X, 1945-7197
Monticone, Silvia and Hattangady, Namita G. and Penton, David and Isales, Carlos M. and Edwards, Michael A. and Williams, Tracy A. and Sterner, Christina and Warth, Richard and Mulatero, Paolo and Rainey, William E. (2013) A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 98 (11). E1861-E1865. ISSN 0021-972X, 1945-7197
T
Tauber, P. and Penton, D. and Stindl, J. and Humberg, E. and Tegtmeier, I. and Sterner, C. and Beuschlein, F. and Reincke, M. and Barhanin, J. and Bandulik, S. and Warth, R. (2014) Pharmacology and Pathophysiology of Mutated KCNJ5 Found in Adrenal Aldosterone-Producing Adenomas. ENDOCRINOLOGY, 155 (4). pp. 1353-1362. ISSN 0013-7227, 1945-7170

