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Autosomal recessive polycystic kidney disease (ARPKD)
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Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease
by Mekahli, Djalila (Author)
, Liebau, Max C. (Author)
, Cadnapaphornchai, Melissa A. (Author)
, Goldstein, Stuart L. (Author)
, Greenbaum, Larry (Author)
, Litwin, Mieczysław (Author)
, Seeman, Tomas (Author)
, Schaefer, Franz (Author)
, Guay-Woodford, Lisa M. (Author)
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BMC nephrology, 24 (2023), Artikel-ID 33, Seite 1-11
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Kidney versus combined kidney and liver transplantation in young people with autosomal recessive polycystic kidney disease: data from the European Society for Pediatric Nephrology/...
by Mekahli, Djalila (Author)
, Schaefer, Franz (Author)
,
in:
American journal of kidney diseases, 68 (2016), 5, Seite 782-788
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Network for early onset cystic kidney diseases: a comprehensive multidisciplinary approach to hereditary cystic kidney diseases in childhood
by König, Jens (Author)
, Lablans, Martin (Author)
, Ückert, Frank (Author)
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Frontiers in Pediatrics, 6 (2018) Artikel-Nummer 24, 9 Seiten
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Medizinische Fakultät Heidelberg
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Klinikum der Universität Heidelberg
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Zentrum für Kinder- und Jugendmedizin
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Mekahli, Djalila
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Schaefer, Franz
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Cadnapaphornchai, Melissa A.
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Goldstein, Stuart L.
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Greenbaum, Larry
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Guay-Woodford, Lisa M.
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König, Jens
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Lablans, Martin
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Liebau, Max C.
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Litwin, Mieczysław
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Seeman, Tomas
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Ückert, Frank
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Autosomal recessive polycystic kidney disease (ARPKD)
Bardet-Biedl syndrome (BBS)
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ESPN/ERA-EDTA Registry
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HNF1B nephropathy
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Tolvaptan
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adolescents
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allograft survival
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children
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ciliopathy
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combined liver-kidney transplantation
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hereditary cystic kidney diseases
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kidney transplantation
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mortality
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nephronophthisis (NPH)
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patient survival
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pediatric
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renal replacement therapy
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young adults
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