Items where Author is "Popp, Bernt"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 2.

Article

Wopperer, Florian J. and Knaup, Karl X. and Stanzick, Kira J. and Schneider, Karen and Jobst-Schwan, Tilman and Ekici, Arif B. and Uebe, Steffen and Wenzel, Andrea and Schliep, Stefan and Schuerfeld, Carsten and Seitz, Randolf and Bernhardt, Wanja and Goedel, Markus and Wiesener, Antje and Popp, Bernt and Stark, Klaus J. and Groene, Hermann-Josef and Friedrich, Bjoern and Weiss, Martin and Basic-Jukic, Nikolina and Schiffer, Mario and Schroeppel, Bernd and Huettel, Bruno and Beck, Bodo B. and Sayer, John A. and Ziegler, Christine and Buettner-Herold, Maike and Amann, Kerstin and Heid, Iris M. and Reis, Andre and Pasutto, Francesca and Wiesener, Michael S. (2022) Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases. KIDNEY INTERNATIONAL, 102 (2). pp. 405-420. ISSN 0085-2538, 1523-1755

Hebebrand, Moritz and Hueffmeier, Ulrike and Trollmann, Regina and Hehr, Ute and Uebe, Steffen and Ekici, Arif B. and Kraus, Cornelia and Krumbiegel, Mandy and Reis, Andre and Thiel, Christian T. and Popp, Bernt (2019) The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy. ORPHANET JOURNAL OF RARE DISEASES, 14: 38. ISSN 1750-1172

This list was generated on Sat Mar 14 10:35:49 2026 CET.