Items where Author is "Cebrian-Serrano, Alberto"

Article

Meindl, Katrin and Issler, Naomi and Afonso, Sara and Cebrian-Serrano, Alberto and Mueller, Karin and Sterner, Christina and Othmen, Helga and Tegtmeier, Ines and Witzgall, Ralph and Klootwijk, Enriko and Davies, Benjamin and Kleta, Robert and Warth, Richard (2023) A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 11: 1240558. ISSN 2296-634X,

Issler, Naomi and Afonso, Sara and Weissman, Irith and Jordan, Katrin and Cebrian-Serrano, Alberto and Meindl, Katrin and Dahlke, Eileen and Tziridis, Konstantin and Yan, Guanhua and Robles-Lopez, Jose M. and Tabernero, Lydia and Patel, Vaksha and Kesselheim, Anne and Klootwijk, Enriko D. and Stanescu, Horia C. and Dumitriu, Simona and Iancu, Daniela and Tekman, Mehmet and Mozere, Monika and Jaureguiberry, Graciana and Outtandy, Priya and Russell, Claire and Forst, Anna-Lena and Sterner, Christina and Heinl, Elena-Sofia and Othmen, Helga and Tegtmeier, Ines and Reichold, Markus and Schiessl, Ina Maria and Limm, Katharina and Oefner, Peter and Witzgall, Ralph and Fu, Lifei and Theilig, Franziska and Schilling, Achim and Biton, Efrat Shuster and Kalfon, Limor and Fedida, Ayalla and Arnon-Sheleg, Elite and Ben Izhak, Ofer and Magen, Daniella and Anikster, Yair and Schulze, Holger and Ziegler, Christine and Lowe, Martin and Davies, Benjamin and Boeckenhauer, Detlef and Kleta, Robert and Zaccai, Tzipora C. Falik and Warth, Richard (2022) A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 33 (4). pp. 732-745. ISSN 1046-6673, 1533-3450

Reichold, Markus and Klootwijk, Enriko D. and Reinders, Joerg and Otto, Edgar A. and Milani, Mario and Broeker, Carsten and Laing, Chris and Wiesner, Julia and Devi, Sulochana and Zhou, Weibin and Schmitt, Roland and Tegtmeier, Ines and Sterner, Christina and Doellerer, Hannes and Renner, Kathrin and Oefner, Peter J. and Dettmer, Katja and Simbuerger, Johann M. and Witzgall, Ralph and Stanescu, Horia C. and Dumitriu, Simona and Iancu, Daniela and Patel, Vaksha and Mozere, Monika and Tekman, Mehmet and Jaureguiberry, Graciana and Issler, Naomi and Kesselheim, Anne and Walsh, Stephen B. and Gale, Daniel P. and Howie, Alexander J. and Martins, Joana R. and Hall, Andrew M. and Kasgharian, Michael and O'Brien, Kevin and Ferreira, Carlos R. and Atwal, Paldeep S. and Jain, Mahim and Hammers, Alexander and Charles-Edwards, Geoffrey and Choe, Chi-Un and Isbrandt, Dirk and Cebrian-Serrano, Alberto and Davies, Ben and Sandford, Richard N. and Pugh, Christopher and Konecki, David S. and Povey, Sue and Bockenhauer, Detlef and Lichter-Konecki, Uta and Gahl, William A. and Unwin, Robert J. and Warth, Richard and Kleta, Robert (2018) Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 29 (7). pp. 1849-1858. ISSN 1046-6673, 1533-3450