Gilbert, Rodney D., Evans, Hazel, Olalekan, Kazeem, Babatunde, Nagra, Arvind, Haq, Mushfequr R. and Griffiths, Mark (2017) Tolvaptan treatment for severe neonatal autosomal-dominant polycystic kidney disease. Pediatric Nephrology, 32 (5), 893-896. (doi:10.1007/s00467-017-3584-9).
Record type:
Article
Abstract
Severe neonatal autosomal-dominant polycystic kidney disease (ADPKD) is rare and easily confused with recessive PKD. Managing such infants is difficult and often unsuccessful.
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s00467-017-3584-9
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Accepted/In Press date: 21 December 2016
e-pub ahead of print date: 13 February 2017
Published date: May 2017
Keywords:
tolvaptan, adpkd, polycystic kidney
Identifiers
Local EPrints ID: 418025
URI: http://eprints.soton.ac.uk/id/eprint/418025
ISSN: 0931-041X
PURE UUID: be165a4c-2205-43d9-bd94-4c402a6b79cc
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Date deposited: 20 Feb 2018 17:34
Last modified: 15 Mar 2024 15:33
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Contributors
Author:
Rodney D. Gilbert
Author:
Hazel Evans
Author:
Kazeem, Babatunde Olalekan
Author:
Arvind Nagra
Author:
Mushfequr R. Haq
Author:
Mark Griffiths
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