The use of sodium DL-3-Hydroxybutyrate in severe acute neuro-metabolic compromise in patients with inherited ketone body synthetic disorders

Metabolic perturbations after pediatric TBI: It's not just about glucose

(2019) Caitlyn E. Bowman et al.   EXPERIMENTAL NEUROLOGY

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Clinical presentation and outcome in a series of 37 patients

(2017) Sarah Catharina Grünert et al.   MOLECULAR GENETICS AND METABOLISM

Glucose feeds the TCA cycle via circulating lactate

(2017) Sheng Hui et al.   NATURE

Ketone body metabolism and its defects

(2014) Toshiyuki Fukao et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Carnitine palmitoyltransferase II (CPT II) deficiency: Genotype–Phenotype analysis of 50 patients

(2013) Pushpa Raj Joshi et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Glucose transporter type I deficiency syndrome: Epilepsy phenotypes and outcomes

(2012) Amanda W. Pong et al.   EPILEPSIA

A series of pregnancies in women with inherited metabolic disease

(2011) Janneke G Langendonk et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Successful Treatment of Severe Cardiomyopathy in Glycogen Storage Disease Type III With D,L-3-Hydroxybutyrate, Ketogenic and High-Protein Diet

(2011) Vassili Valayannopoulos et al.   PEDIATRIC RESEARCH

Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis

(2009) CHRISTINE BARNERIAS et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY