Resultados de procura - Sterner, Christina
- Mostrando 1 - 9 Resultados de 9
-
1
Validation of the Rainbow Model of Integrated Care Measurement Tools (RMIC-MTs) in renal care for patient and care providers por Valentijn, Pim P., Pereira, Fernando, Sterner, Christina W., Vrijhoef, Hubertus J. M., Ruwaard, Dirk, Hegbrant, Jörgen, Strippoli, Giovanni F. M.
Publicado 2019Text -
2
A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III por Monticone, Silvia, Hattangady, Namita G., Penton, David, Isales, Carlos M., Edwards, Michael A., Williams, Tracy A., Sterner, Christina, Warth, Richard, Mulatero, Paolo, Rainey, William E.
Publicado 2013Text -
3
Person-Centered Integrated Care for Chronic Kidney Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials por Valentijn, Pim P., Pereira, Fernando Abdalla, Ruospo, Marinella, Palmer, Suetonia C., Hegbrant, Jörgen, Sterner, Christina W., Vrijhoef, Hubertus J.M., Ruwaard, Dirk, Strippoli, Giovanni F.M.
Publicado 2018Text -
4
KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function por Reichold, Markus, Zdebik, Anselm A., Lieberer, Evelyn, Rapedius, Markus, Schmidt, Katharina, Bandulik, Sascha, Sterner, Christina, Tegtmeier, Ines, Penton, David, Baukrowitz, Thomas, Hulton, Sally-Anne, Witzgall, Ralph, Ben-Zeev, Bruria, Howie, Alexander J., Kleta, Robert, Bockenhauer, Detlef, Warth, Richard
Publicado 2010Text -
5
Task2 potassium channels set central respiratory CO(2) and O(2) sensitivity por Gestreau, Christian, Heitzmann, Dirk, Thomas, Joerg, Dubreuil, Véronique, Bandulik, Sascha, Reichold, Markus, Bendahhou, Saïd, Pierson, Patricia, Sterner, Christina, Peyronnet-Roux, Julie, Benfriha, Chérif, Tegtmeier, Ines, Ehnes, Hannah, Georgieff, Michael, Lesage, Florian, Brunet, Jean-Francois, Goridis, Christo, Warth, Richard, Barhanin, Jacques
Publicado 2010Text -
6
Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis por Heitzmann, Dirk, Derand, Renaud, Jungbauer, Stefan, Bandulik, Sascha, Sterner, Christina, Schweda, Frank, Wakil, Abeer El, Lalli, Enzo, Guy, Nicolas, Mengual, Raymond, Reichold, Markus, Tegtmeier, Ines, Bendahhou, Saïd, Gomez-Sanchez, Celso E, Isabel Aller, M, Wisden, William, Weber, Achim, Lesage, Florian, Warth, Richard, Barhanin, Jacques
Publicado 2008Text -
7
Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations por Bockenhauer, Detlef, Feather, Sally, Stanescu, Horia C., Bandulik, Sascha, Zdebik, Anselm A., Reichold, Markus, Tobin, Jonathan, Lieberer, Evelyn, Sterner, Christina, Landoure, Guida, Arora, Ruchi, Sirimanna, Tony, Thompson, Dorothy, Cross, J. Helen, Hoff, William van’t, Masri, Omar Al, Tullus, Kjell, Yeung, Stella, Anikster, Yair, Klootwijk, Enriko, Hubank, Mike, Dillon, Michael J., Heitzmann, Dirk, Arcos-Burgos, Mauricio, Knepper, Mark A., Dobbie, Angus, Gahl, William A., Warth, Richard, Sheridan, Eamonn, Kleta, Robert
Publicado 2009Text -
8
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness por Issler, Naomi, Afonso, Sara, Weissman, Irith, Jordan, Katrin, Cebrian-Serrano, Alberto, Meindl, Katrin, Dahlke, Eileen, Tziridis, Konstantin, Yan, Guanhua, Robles-López, José M., Tabernero, Lydia, Patel, Vaksha, Kesselheim, Anne, Klootwijk, Enriko D., Stanescu, Horia C., Dumitriu, Simona, Iancu, Daniela, Tekman, Mehmet, Mozere, Monika, Jaureguiberry, Graciana, Outtandy, Priya, Russell, Claire, Forst, Anna-Lena, Sterner, Christina, Heinl, Elena-Sofia, Othmen, Helga, Tegtmeier, Ines, Reichold, Markus, Schiessl, Ina Maria, Limm, Katharina, Oefner, Peter, Witzgall, Ralph, Fu, Lifei, Theilig, Franziska, Schilling, Achim, Shuster Biton, Efrat, Kalfon, Limor, Fedida, Ayalla, Arnon-Sheleg, Elite, Ben Izhak, Ofer, Magen, Daniella, Anikster, Yair, Schulze, Holger, Ziegler, Christine, Lowe, Martin, Davies, Benjamin, Böckenhauer, Detlef, Kleta, Robert, Falik Zaccai, Tzipora C., Warth, Richard
Publicado 2022Text -
9
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure por Reichold, Markus, Klootwijk, Enriko D., Reinders, Joerg, Otto, Edgar A., Milani, Mario, Broeker, Carsten, Laing, Chris, Wiesner, Julia, Devi, Sulochana, Zhou, Weibin, Schmitt, Roland, Tegtmeier, Ines, Sterner, Christina, Doellerer, Hannes, Renner, Kathrin, Oefner, Peter J., Dettmer, Katja, Simbuerger, Johann M., Witzgall, Ralph, Stanescu, Horia C., Dumitriu, Simona, Iancu, Daniela, Patel, Vaksha, Mozere, Monika, Tekman, Mehmet, Jaureguiberry, Graciana, Issler, Naomi, Kesselheim, Anne, Walsh, Stephen B., Gale, Daniel P., Howie, Alexander J., Martins, Joana R., Hall, Andrew M., Kasgharian, Michael, O’Brien, Kevin, Ferreira, Carlos R., Atwal, Paldeep S., Jain, Mahim, Hammers, Alexander, Charles-Edwards, Geoffrey, Choe, Chi-Un, Isbrandt, Dirk, Cebrian-Serrano, Alberto, Davies, Ben, Sandford, Richard N., Pugh, Christopher, Konecki, David S., Povey, Sue, Bockenhauer, Detlef, Lichter-Konecki, Uta, Gahl, William A., Unwin, Robert J., Warth, Richard, Kleta, Robert
Publicado 2018Text