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Klinische Padiatrie|January 11, 2019
Anna-Lena Sieg, Anibh Martin Das, Nicole Maria Muschol, et al.
Oxidative Medicine and Cellular Longevity|April 24, 2014
L-arginine/NO pathway is altered in children with haemolytic-uraemic syndrome (HUS)Nele Kirsten Kanzelmeyer, Lars Pape, Kristine Chobanyan-Jürgens, et al.
Amino Acids|January 4, 2019
Development and validation of GC-MS methods for the comprehensive analysis of amino acids in plasma and urine and applications to the HELLP syndrome and pediatric kidney transplantation: evidence of altered methylation, transamidination, and arginase activityErik Hanff, Stephan Ruben, Martin Kreuzer, et al.
Nutrients|January 5, 2021
Hepatorenal Tyrosinaemia: Impact of a Simplified Diet on Metabolic Control and Clinical OutcomeFriederike Bärhold, Uta Meyer, Anne-Kathrin Neugebauer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2020
Galactokinase deficiency: lessons from the GalNet registryM Estela Rubio-Gozalbo, Britt Derks, Anibh Martin Das, et al.
Journal of Inherited Metabolic Disease|December 15, 2017
An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variantsAna Pop, Monique Williams, Eduard A Struys, et al.
Orphanet Journal of Rare Diseases|August 2, 2014
Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practiceSebene Mayorandan, Uta Meyer, Gülden Gokcay, et al.
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