Journal of Inherited Metabolic Disease

Preface

Gamma-hydroxybutyric aciduria: A biochemist’s education from a heritable disorder of GABA metabolism

K. M. Gibson

Dominantly inherited hyperinsulinaemic hypoglycaemia

P. De Lonlay, I. Giurgea, C. Sempoux, G. Touati, F. Jaubert, J. Rahier, M. Ribeiro, F. Brunelle, C. Nihoul-Fékété, J.-J. Robert, J.-M. Saudubray, C. Stanley, C. Bellanné-Chantelot

Molecular mechanisms of dominant expression in porphyria

M. N. Badminton, G. H. Elder

Dominance in mitochondrial disorders

M. Zeviani, V. Carelli

Molecular mechanism of dominant expression in 3-methylcrotonyl-CoA carboxylase deficiency

M. R. Baumgartner

Magnetic resonance techniques in the assessment of myelin and myelination

A. J. Barkovich

Disorders of intermediary metabolism: Toxic leukoencephalopathies

F. Hörster, R. Surtees, G. F. Hoffmann

Oligodendrocytes and stem cell transplantation: their potential in the treatment of leukoencephalopathies

I. D. Duncan

Peroxisome biogenesis disorders: The role of peroxisomes and metabolic dysfunction in developing brain

P. L. Faust, D. Banka, R. Siriratsivawong, V. G. Ng, T. M. Wikander

Congenital brain anomalies in distal cholesterol biosynthesis defects

R. C. M. Hennekam

Congenital brain malformations in mitochondrial disease

G. K. Brown

Acute metabolic encephalopathy: An introduction

J. V. Leonard

Urea cycle defects: Management and outcome

M. C. Nassogne, B. Héron, G. Touati, D. Rabier, J. M. Saudubray

Methylmalonic and propionic acidaemias: Management and outcome

H. Ogier De Baulny, J. F. Benoist, O. Rigal, G. Touati, D. Rabier, J. M. Saudubray

Movement disorders: Classifications

C. Klein

Treatment strategies in movement disorders

J. D. Speelman