Florian B. Lagler

Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency

Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg et al. · Pediatric Research · 2006 · 266 citations · Full text

Nutrition, Metabolic Disorder, Pediatric Hematology +8

Structural and functional rejuvenation of the aged brain by an approved anti-asthmatic drug

Julia Marschallinger, Iris Schäffner, Barbara Klein et al. · Nature Communications · 2015 · 191 citations · Full text

Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor

Saskia B. Wortmann, Johan L.K. Van Hove, Terry G. J. Derks et al. · Blood · 2020 · 173 citations · Full text

Loss of Function in Phenylketonuria Is Caused by Impaired Molecular Motions and Conformational Instability

Søren W. Gersting, Kristina Kemter, Michael Staudigl et al. · The American Journal of Human Genetics · 2008 · 120 citations · Full text

Biophysical Modeling, Protein Function, Biochemistry +12

Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity ofMCCA andMCCB mutations and impact on risk assessment

Sonja C. Stadler, Roman Polanetz, Esther M. Maier et al. · Human Mutation · 2006 · 89 citations