Ulrike Mutze

Heidelberg, BW 69120, Germany

Last Updated: 09/26/2026

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Found 61 publications

Reference values for serum proenkephalin in a pediatric and young adult cohort.

Reference values for serum proenkephalin in a pediatric and young adult cohort.

Journal: Clinical biochemistry

Published: July 09, 2026

Prevalence, Disease Onset and Clinical Outcome in Arginase 1 Deficiency: Cross-Border Surveillance in Germany, Austria, and Switzerland.

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

MR Neurography in Children and Adolescents: Multiparametric Assessment of Peripheral Nerve Involvement in Long-chain Fatty Acid Oxidation Disorders.

MR Neurography in Children and Adolescents: Multiparametric Assessment of Peripheral Nerve Involvement in Long-chain Fatty Acid Oxidation Disorders.

Journal: Investigative radiology

Published: November 18, 2025

Diagnostic delay in inherited metabolic diseases: Insights from the U-IMD registry.

Diagnostic delay in inherited metabolic diseases: Insights from the U-IMD registry.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 31, 2025

Newborn Screening for Urea Cycle Disorders and Clinical Outcomes.

Newborn Screening for Urea Cycle Disorders and Clinical Outcomes.

Journal: Pediatrics

Published: August 31, 2025

A multi-dimensional framework for establishing and managing a genomic newborn screening program.

A multi-dimensional framework for establishing and managing a genomic newborn screening program.

Journal: European journal of human genetics : EJHG

Published: August 13, 2025

A population-representative survey on attitudes toward genomic newborn screening in Germany.

A population-representative survey on attitudes toward genomic newborn screening in Germany.

Journal: Genetics in medicine open

Published: July 22, 2025

Direct Prediction of VLCADD Severity Using Newborn Screening Analyte Data.

Direct Prediction of VLCADD Severity Using Newborn Screening Analyte Data.

Journal: Journal of inherited metabolic disease

Published: July 15, 2025

Trial Readiness: Understanding the Natural History of Rare Diseases.

Trial Readiness: Understanding the Natural History of Rare Diseases.

Journal: Journal of inherited metabolic disease

Published: June 11, 2025

Impact of Newborn Screening on Survival and Developmental Outcome in Classic Isovaleric Aciduria: A Meta-Analysis.

Impact of Newborn Screening on Survival and Developmental Outcome in Classic Isovaleric Aciduria: A Meta-Analysis.

Journal: Journal of inherited metabolic disease

Published: June 04, 2025

Response to Downie et al.

Response to Downie et al.

Journal: Journal of inherited metabolic disease

Published: December 08, 2024

Newborn screening for neuro-metabolic disorders: Strategies, clinical benefits, and prerequisites for program expansion.

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

Showing 1-12 of 61

Last Updated: 09/26/2026