Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD)

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)

Subject

Multidisciplinary

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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