Svenja Scharre
Heidelberg, BW, Germany
Last Updated: 09/26/2026
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Found 8 publications
Prevalence, Disease Onset and Clinical Outcome in Arginase 1 Deficiency: Cross-Border Surveillance in Germany, Austria, and Switzerland.
Journal: Journal of inherited metabolic disease
Published: March 11, 2026
Newborn Screening for Urea Cycle Disorders and Clinical Outcomes.
Journal: Pediatrics
Published: August 31, 2025
Newborn screening for neuro-metabolic disorders: Strategies, clinical benefits, and prerequisites for program expansion.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: October 30, 2024
Impact of early diagnosis, disease variant, and quality of care on the neurocognitive outcome in maple syrup urine disease: A meta-analysis.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 18, 2024
Severity-adjusted evaluation of liver transplantation on health outcomes in urea cycle disorders.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 23, 2023
ASS1 deficiency is associated with impaired neuronal differentiation in zebrafish larvae.
Journal: Molecular genetics and metabolism
Published: July 18, 2023
Predicting the disease severity in male individuals with ornithine transcarbamylase deficiency.
Journal: Annals of clinical and translational neurology
Published: June 04, 2022
Severity-adjusted evaluation of newborn screening on the metabolic disease course in individuals with cytosolic urea cycle disorders.
Journal: Molecular genetics and metabolism
Published: August 20, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026