Peter Burgard
Heidelberg, BW, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 65 publications
Correspondence on "Phenylalanine hydroxylase deficiency diagnosis and management: A 2023 evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)" by Smith et al.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 16, 2025
Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening.
Journal: Journal of inherited metabolic disease
Published: April 25, 2024
Resource use and costs of transitioning from paediatric to adult care for patients with chronic endocrine disease.
Journal: Clinical endocrinology
Published: February 20, 2024
Resource utilization and costs of transitioning from pediatric to adult care for patients with chronic autoinflammatory and autoimmune disorders.
Journal: Pediatric rheumatology online journal
Published: December 28, 2023
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias.
Journal: Journal of inherited metabolic disease
Published: September 16, 2023
Resource use and costs of transitioning from pediatric to adult care for patients with chronic kidney disease.
Journal: Pediatric nephrology (Berlin, Germany)
Published: April 04, 2023
Transition for adolescents with a rare disease: results of a nationwide German project.
Journal: Orphanet journal of rare diseases
Published: September 22, 2022
Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision.
Journal: Journal of inherited metabolic disease
Published: July 19, 2022
Impact of pregnancy planning and preconceptual dietary training on metabolic control and offspring's outcome in phenylketonuria.
Journal: Journal of inherited metabolic disease
Published: March 14, 2022
Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This Observation.
Journal: Metabolites
Published: September 13, 2021
Impact of glycogen storage disease type I on adult daily life: a survey.
Journal: Orphanet journal of rare diseases
Published: April 19, 2021
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee.
Journal: Orphanet journal of rare diseases
Published: April 01, 2021
Last Updated: 09/26/2026