Stefan Kölker

1. Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision
   2022/10/12 by Nikolas Boy, Chris Mühlhausen, Esther M. Maier +32 · 4 citations
   Biochemistry, Genetics and Molecular Biology · #Biochemical and Molecular Research #Metabolism and Genetic Disorders #Mitochondrial Function and Pathology
2. Neonatal screening for glutaryl‐CoA dehydrogenase deficiency
   2004/10/26 by M. Lindner, Martin Lindner, S. KÖlker +8 · 2 citations
   Biochemistry, Genetics and Molecular Biology · Medicine · #Diet and metabolism studies #Metabolism and Genetic Disorders
3. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision
   2016/11/16 by Nikolas Boy, Chris Mühlhausen, Esther M. Maier +20 · 2 citations
   Biochemistry, Genetics and Molecular Biology · #Biochemical and Molecular Research #Metabolism and Genetic Disorders #Mitochondrial Function and Pathology