Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU)
Martina Huemer(University Children's Hospital Zurich), Olaf A. Bodamer(Broad Institute), Adolf Mühl(Medical University of Vienna), Hanno Ulmer(Innsbruck Medical University), D Mayr(Landeskrankenhaus Feldkirch), Dorothea Möslinger(Medical University of Vienna), B. Simma(Landeskrankenhaus Feldkirch), Inès Schmid
Cited by 23
Related Papers
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease
|New England Journal of Medicine|2019|823
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
|Orphanet Journal of Rare Diseases|2014|713
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
|European Journal of Pediatrics|2007|535
Guidelines for the diagnosis and management of cystathionine beta‐synthase deficiency
|Journal of Inherited Metabolic Disease|2016|335
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia
|Nature Communications|2016|326