All papers authored by Detlef Bockenhauer
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2020
Larissa P. Govers,
Hakan R. Toka,
Ali Hariri,
Stephen B. Walsh 
,
Detlef Bockenhauer
,
Detlef Bockenhauer
Mitochondrial DNA mutations in renal disease: an overview
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2018
Markus Reichold,
Enriko D. Klootwijk,
Joerg Reinders,
Edgar A. Otto,
Mario Milani,
Carsten Broeker,
Chris Laing,
Julia Wiesner,
Sulochana Devi,
Weibin Zhou,
Roland Schmitt,
Ines Tegtmeier,
Christina Sterner,
Hannes Doellerer,
Kathrin Renner
and 39 other authors
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
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2017
Sven Enerbäck ,
Daniel Nilsson,
Noel Edwards,
Mikael Heglind,
Sumaya Alkanderi,
Emma Ashton,
Asma Deeb,
Feras E. B. Kokash,
Abdulrahim R. A. Bakhsh,
William van’t Hoff,
Stephen B. Walsh ,
Felice D’Arco,
Arezoo Daryadel,
Soline Bourgeois,
Carsten A. Wagner
and 3 other authors
,
Daniel Nilsson,
Noel Edwards,
Mikael Heglind,
Sumaya Alkanderi,
Emma Ashton,
Asma Deeb,
Feras E. B. Kokash,
Abdulrahim R. A. Bakhsh,
William van’t Hoff,
Stephen B. Walsh ,
Felice D’Arco,
Arezoo Daryadel,
Soline Bourgeois,
Carsten A. Wagner
and 3 other authors
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1
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Patrick R. Walsh,
Yincent Tse,
Emma Ashton,
Daniela Iancu,
Lucy Jenkins,
Marc Bienias,
Robert Kleta,
William van’t Hoff,
Detlef Bockenhauer
Clinical and diagnostic features of Bartter and Gitelman syndromes
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Detlef Bockenhauer
Hyponatremia and cyst growth in neonatal polycystic kidney disease: a case for aquaretics?
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2016
Ola Abdelhadi ,
Daniela Iancu,
Horia Stanescu,
Robert Kleta ,
Detlef Bockenhauer
,
Daniela Iancu,
Horia Stanescu,
Robert Kleta ,
Detlef Bockenhauer
EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10.
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