Use of guidelines improves the neurological outcome in glutaric aciduria type IJana Herınger, Stefan Kölker, Chris Mühlhausen et al.|Annals of Neurology|2010Cited by 169
Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in GermanyStefan Kölker, Georg F. Hoffmann, Sven F. Garbade et al.|Pediatric Research|2007Cited by 111
Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaireSarah C. Grünert, Hester C. Schuman, Terry G. J. Derks et al.|Genetics in Medicine|2022Cited by 64
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorderPauline E. Schneeberger, Ashley Andrews, Fanny Kortüm et al.|Brain|2020Cited by 59