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