Results 221 to 230 of about 95,428 (234)

Dent Disease 1

2009
Dieter Metze, Tam Nguyen, Birgit Haack, Alexander K. C. Leung, Noriko Miyake, Naomichi Matsumoto, A. J. Larner, Oliver Bartsch, Barbara C. Van Munster, Christine A. F. Von Arnim, Jochen Klucken, Peter Heutink, Chaeyoung Lee, Alexander K. C. Leung, Alexander A. C. Leung, Justine H. S. Fong, Silke Hofmann, Leena Bruckner-Tuderman, Anca Sindrilaru, Cord Sunderkötter, Lev G. Goldfarb, Andreas Barthel, Erwin Schleicher, Andreas Fritsche, Derek LeRoith, Gunter Wolf, Wilgard Hunger-Dathe, John-John B. Schnog, Victor E. A. Gerdes, Michael Benatar, Michael Fromm, Jörg-Dieter Schulzke, Stefan Bröer, André B. P. Van Kuilenburg, Albert H. Van Gennip*, André B. P. Kuilenburg, Albert H. Gennip*, Michael Straub, Albrecht Hesse, Hugo Ten Cate, Nigel Laing, Frank Mastaglia, Manish Suneja, Christie P. Thomas, Ulrich Müller, Birgit Zirn, Daniela Steinberger, Mary Redmond Hutson, Margaret L. Kirby, Peter L. M. Jansen, Sönke Weihe, Jan Schulte Am Esch, Wolfram Trudo Knoefel, Alexander K. C. Leung, Andrew L. Wong, Noriko Miyake, Naomichi Matsumoto, August H. M. Smelt, Dieter Metze, Johannes Schumacher, Per Hoffmann, Markus M. Nöthen, Andrea Schuppenies, Markus G. Donner, Dieter Häussinger, Norman Kock, Katja Lohmann, Christine Klein   +67 more
openaire   +1 more source

Locus heterogeneity of Dent’s disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations

Pediatric Nephrology, 2009
Gianluca Caridi, Franca Anglani, Gian Marco Ghiggeri   +2 more
exaly  

Dent's disease

2000
openaire   +1 more source

From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes

Human Mutation, 2011
Genevieve Baujat, Véronique Satre, John Rendu   +2 more
exaly  

A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5

European Journal of Pediatrics, 2011
Takayuki Okamoto, Okamoto Takayuki, Tajima Toshihiro   +2 more
exaly  

Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease

American Journal of Kidney Diseases, 2006
Velibor Tasic, Arend Bokenkamp, Michael Ludwig   +2 more
exaly  

ClC-5 mutations associated with Dent’s disease: a major role of the dimer interface

Pflugers Archiv European Journal of Physiology, 2011
Stéphane Lourdel, Wendy Gonzalez, FRANCISCO V Sepulveda   +2 more
exaly  

Dent's Disease

2009
openaire   +1 more source

[Dent's disease].

Nihon rinsho. Japanese journal of clinical medicine, 2006
openaire   +1 more source

Dent Disease (Xp11.22)

2008
openaire   +1 more source