Author:
Laemmle Alexander,Gallagher Renata C.,Keogh Adrian,Stricker Tamar,Gautschi Matthias,Nuoffer Jean-Marc,Baumgartner Matthias R.,Häberle Johannes
Funder
EMDO Stiftung Zurich
Forschungszentrum Kind (FZK) – University Children`s Hospital Zurich
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Rare Disease Initiative Zurich (radiz)
National Institutes of Health (NIH) Rare Disease Clinical Research Network (RDCRN)
Office of Rare Diseases Research
the National Center for Advancing Translational Science
Eunice Kennedy Shriver National Institute of Child Health and Human Development
O’Malley 332 Foundation
the Rotenberg Family Fund
the Dietmar-Hopp Foundation
the Kettering Fund
Publisher
Public Library of Science (PLoS)
Reference41 articles.
1. Clinical and biochemical aspects of primary and secondary hyperammonemic disorders;J Haberle;Arch Biochem Biophys,2013
2. Suggested guidelines for the diagnosis and management of urea cycle disorders;J Haberle;Orphanet J Rare Dis,2012
3. The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation;S Kolker;J Inherit Metab Dis,2015
4. Metabolic investigations prevent liver transplantation in two young children with citrullinemia type I;MJ de Groot;J Inherit Metab Dis,2011
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