نتائج البحث - Sterner, Christina

Validation of the Rainbow Model of Integrated Care Measurement Tools (RMIC-MTs) in renal care for patient and care providers حسب Valentijn, Pim P., Pereira, Fernando, Sterner, Christina W., Vrijhoef, Hubertus J. M., Ruwaard, Dirk, Hegbrant, Jörgen, Strippoli, Giovanni F. M.

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III حسب 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.

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Person-Centered Integrated Care for Chronic Kidney Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials حسب 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.

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function حسب 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

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Task2 potassium channels set central respiratory CO(2) and O(2) sensitivity حسب 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

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis حسب 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

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations حسب 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

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness حسب 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

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure حسب 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

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل