Research highlights

1. Glucose transporter deficiency syndrome

2 MELAS (mitochondrial encephalopathy, lactic acidosis and stroke- like episodes) therapy

3 MELAS natural history

4 Sickle cell disease encephalopathy

5 Novel chemotherapeutic agents for brain tumors

6 Ion channel diseases

7 Pyruvate dehydrogenase deficiency

8 Pyruvate carboxylase deficiency

9 Transgenic animal models of human disease

10 Metabolic imaging of the developing human brain

11 Gene induction therapies

12 Molecular and genetic diagnosis

13 Newborn neuromuscular diseases (spinal muscular atrophy)

14 Reye syndrome