Kết quả tìm kiếm - Sterner, Christina
- Đang hiển thị 1 - 9 kết quả của 9
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1
Validation of the Rainbow Model of Integrated Care Measurement Tools (RMIC-MTs) in renal care for patient and care providers Bằng Valentijn, Pim P., Pereira, Fernando, Sterner, Christina W., Vrijhoef, Hubertus J. M., Ruwaard, Dirk, Hegbrant, Jörgen, Strippoli, Giovanni F. M.
Được phát hành 2019Text -
2
A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III Bằng 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.
Được phát hành 2013Text -
3
Person-Centered Integrated Care for Chronic Kidney Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials Bằng 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.
Được phát hành 2018Text -
4
KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function Bằng 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
Được phát hành 2010Text -
5
Task2 potassium channels set central respiratory CO(2) and O(2) sensitivity Bằng 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
Được phát hành 2010Text -
6
Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis Bằng 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
Được phát hành 2008Text -
7
Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations Bằng 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
Được phát hành 2009Text -
8
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness Bằng 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
Được phát hành 2022Text -
9
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure Bằng 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
Được phát hành 2018Text