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Volume 28, Number 3, May 2005

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Preface
pp. 245-246(2)

Dominantly inherited hyperinsulinaemic hypoglycaemia
pp. 267-276(10)
Authors: Lonlay, P.; Giurgea, I.; Sempoux, C.; Touati, G.; Jaubert, F.; Rahier, J.; Ribeiro, M.; Brunelle, F.; Nihoul-Fékété, C.; Robert, J.-J.; Saudubray, J.-M.; Stanley, C.; Bellanné-Chantelot, C.

Molecular mechanisms of dominant expression in porphyria
pp. 277-286(10)
Authors: Badminton, M.; Elder, G.

Dominance in mitochondrial disorders
pp. 287-299(13)
Authors: Zeviani, M.; Carelli, V.

Disorders of intermediary metabolism: Toxic leukoencephalopathies
pp. 345-356(12)
Authors: Hörster, F.; Surtees, R.; Hoffmann, G.

Peroxisome biogenesis disorders: The role of peroxisomes and metabolic dysfunction in developing brain
pp. 369-383(15)
Authors: Faust, P.; Banka, D.; Siriratsivawong, R.; Ng, V.; Wikander, T.

Acute metabolic encephalopathy: An introduction
pp. 403-406(4)
Author: Leonard, J.

Urea cycle defects: Management and outcome
pp. 407-414(8)
Authors: Nassogne, M.; Héron, B.; Touati, G.; Rabier, D.; Saudubray, J.

Methylmalonic and propionic acidaemias: Management and outcome
pp. 415-423(9)
Authors: Baulny, H.; Benoist, J.; Rigal, O.; Touati, G.; Rabier, D.; Saudubray, J.

Movement disorders: Classifications
pp. 425-439(15)
Author: Klein, C.

Treatment strategies in movement disorders
pp. 441-444(4)
Author: Speelman, J.

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