Disorders of intermediary metabolism: Toxic leukoencephalopathies.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 345, doi. 10.1007/s10545-005-2164-5
- By:
- Publication type:
- Article
Works matching IS 01418955 AND DT 2005 AND VI 28 AND IP 3
Results: 17
1
2
Urea cycle defects: Management and outcome.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 407, doi. 10.1007/s10545-005-0303-7
- By:
- Publication type:
- Article
3
Dominance in mitochondrial disorders.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 287, doi. 10.1007/s10545-005-0307-3
- By:
- Publication type:
- Article
4
Preface.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 245, doi. 10.1007/s10545-005-4127-2
- Publication type:
- Article
5
Magnetic resonance techniques in the assessment of myelin and myelination.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 311, doi. 10.1007/s10545-005-5952-z
- By:
- Publication type:
- Article
6
Congenital brain malformations in mitochondrial disease.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 393, doi. 10.1007/s10545-005-7051-6
- By:
- Publication type:
- Article
7
Gamma-hydroxybutyric aciduria: A biochemist’s education from a heritable disorder of GABA metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 247, doi. 10.1007/s10545-005-7053-4
- By:
- Publication type:
- Article
8
Molecular mechanism of dominant expression in 3-methylcrotonyl-CoA carboxylase deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 301, doi. 10.1007/s10545-005-7054-3
- By:
- Publication type:
- Article
9
Congenital brain anomalies in distal cholesterol biosynthesis defects.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 385, doi. 10.1007/s10545-005-7055-2
- By:
- Publication type:
- Article
10
Methylmalonic and propionic acidaemias: Management and outcome.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 415, doi. 10.1007/s10545-005-7056-1
- By:
- Publication type:
- Article
11
Dominantly inherited hyperinsulinaemic hypoglycaemia.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 267, doi. 10.1007/s10545-005-7057-0
- By:
- Publication type:
- Article
12
Oligodendrocytes and stem cell transplantation: their potential in the treatment of leukoencephalopathies.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 357, doi. 10.1007/s10545-005-7058-z
- By:
- Publication type:
- Article
13
Peroxisome biogenesis disorders: The role of peroxisomes and metabolic dysfunction in developing brain.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 369, doi. 10.1007/s10545-005-7059-y
- By:
- Publication type:
- Article
14
Movement disorders: Classifications.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 425, doi. 10.1007/s10545-005-7495-8
- By:
- Publication type:
- Article
15
Acute metabolic encephalopathy: An introduction.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 403, doi. 10.1007/s10545-005-8047-y
- By:
- Publication type:
- Article
16
Treatment strategies in movement disorders.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 441, doi. 10.1007/s10545-005-8049-9
- By:
- Publication type:
- Article
17
Molecular mechanisms of dominant expression in porphyria.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 277, doi. 10.1007/s10545-005-8050-3
- By:
- Publication type:
- Article