Florian B. Lagler
Paracelsus Medical University(AT)
Publications by Year
Research Areas
Lysosomal Storage Disorders Research, Pharmaceutical studies and practices, Metabolism and Genetic Disorders, Glycogen Storage Diseases and Myoclonus, Mitochondrial Function and Pathology
Most-Cited Works
- → Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency(2006)268 cited
- → Structural and functional rejuvenation of the aged brain by an approved anti-asthmatic drug(2015)191 cited
- → Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor(2020)176 cited
- → Loss of Function in Phenylketonuria Is Caused by Impaired Molecular Motions and Conformational Instability(2008)121 cited
- → Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity ofMCCA andMCCB mutations and impact on risk assessment(2006)89 cited
- → International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria(2019)72 cited
- → Diacerein orphan drug development for epidermolysis bullosa simplex: A phase 2/3 randomized, placebo-controlled, double-blind clinical trial(2018)68 cited
- → A 6‐month randomized, double‐blind, placebo‐controlled trial of weekly exenatide in adolescents with obesity(2020)68 cited
- → Novel pharmacological chaperones that correct phenylketonuria in mice(2012)66 cited
- → Topical diacerein for epidermolysis bullosa: a randomized controlled pilot study(2013)61 cited