Martin Lindner
Frankfurt Am Main, HE, Germany
Last Updated: 09/26/2026
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Found 45 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
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
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders.
Journal: Annals of clinical and translational neurology
Published: December 14, 2023
Treatment Outcomes for Maple Syrup Urine Disease Detected by Newborn Screening.
Journal: Pediatrics
Published: September 19, 2023
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias.
Journal: Journal of inherited metabolic disease
Published: September 16, 2023
Isovaleric aciduria identified by newborn screening: Strategies to predict disease severity and stratify treatment.
Journal: Journal of inherited metabolic disease
Published: January 25, 2023
Impact of the SARS-CoV-2 pandemic on the health of individuals with intoxication-type metabolic diseases-Data from the E-IMD consortium.
Journal: Journal of inherited metabolic disease
Published: August 17, 2022
Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision.
Journal: Journal of inherited metabolic disease
Published: July 19, 2022
Long-term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening.
Journal: Journal of inherited metabolic disease
Published: May 16, 2022
Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 25, 2022
Publisher Correction: The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study.
Journal: Scientific reports
Published: October 13, 2021
The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study.
Journal: Scientific reports
Published: June 14, 2021
Last Updated: 09/26/2026