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Getting the diagnostic clue, role of MRI in the diagnosis of type 1 Glutaric aciduria in resource limited settings ScienceDirect Teaching NeuroImages: Glutaric aciduria type 1 (glutaryl CoA dehydrogenase deficiency) Neurology Systematic Approach to Diagnose Inborn Neurometabolic Disorders IntechOpen Clinico radiological phenotyping and diagnostic pathways in childhood neurometabolic disordersa practical introductory guide Biswas Translational Pediatrics Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome Italian Journal of Pediatrics Springer Nature Link
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