All papers authored by Robert Kleta
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2020
Eszter Balogh 
,
Jennifer C. Chandler ,
Máté Varga ,
Mona Tahoun,
Dóra K. Menyhárd,
Gusztáv Schay ,
Tomas Goncalves,
Renáta Hamar,
Regina Légrádi ,
Ákos Szekeres,
Olivier Gribouval ,
Robert Kleta ,
Horia Stanescu,
Detlef Bockenhauer ,
Andrea Kerti
and 42 other authors
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,
Jennifer C. Chandler ,
Máté Varga ,
Mona Tahoun,
Dóra K. Menyhárd,
Gusztáv Schay ,
Tomas Goncalves,
Renáta Hamar,
Regina Légrádi ,
Ákos Szekeres,
Olivier Gribouval ,
Robert Kleta ,
Horia Stanescu,
Detlef Bockenhauer ,
Andrea Kerti
and 42 other authors
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Jingyuan Xie,
Lili Liu ,
Nikol Mladkova,
Yifu Li,
Hong Ren,
Weiming Wang,
Zhao Cui,
Li Lin,
Xiaofan Hu,
Xialian Yu,
Jing Xu,
Gang Liu,
Yasar Caliskan,
Carlo Sidore,
Olivia Balderes
and 105 other authors
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,
Nikol Mladkova,
Yifu Li,
Hong Ren,
Weiming Wang,
Zhao Cui,
Li Lin,
Xiaofan Hu,
Xialian Yu,
Jing Xu,
Gang Liu,
Yasar Caliskan,
Carlo Sidore,
Olivia Balderes
and 105 other authors
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2019
Stephanie Dufek,
Chris Cheshire,
Adam P. Levine ,
Richard S. Trompeter,
Naomi Issler,
Matthew Stubbs,
Monika Mozere,
Sanjana Gupta,
Enriko Klootwijk,
Vaksha Patel,
Daljit Hothi,
Aoife Waters,
Hazel Webb,
Kjell Tullus,
Lucy Jenkins
and 20 other authors
,
Richard S. Trompeter,
Naomi Issler,
Matthew Stubbs,
Monika Mozere,
Sanjana Gupta,
Enriko Klootwijk,
Vaksha Patel,
Daljit Hothi,
Aoife Waters,
Hazel Webb,
Kjell Tullus,
Lucy Jenkins
and 20 other authors
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome
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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
,
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
Download from discovery.ucl.ac.uk
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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Stephen Benedict Walsh ,
Robert Unwin,
Robert Kleta ,
William van’t Hoff,
Paul Bass,
Khalid Hussain,
Sian Ellard,
Detlef Bockenhauer
,
Robert Unwin,
Robert Kleta ,
William van’t Hoff,
Paul Bass,
Khalid Hussain,
Sian Ellard,
Detlef Bockenhauer
Fainting Fanconi syndrome clarified by proxy: a case report
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2016
Ben Oliveira,
Robert Kleta ,
Detlef Bockenhauer,
Stephen B. Walsh
,
Detlef Bockenhauer,
Stephen B. Walsh
Genetic, pathophysiological, and clinical aspects of nephrocalcinosis
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