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At a glance: The STEP trials

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Journal of Inherited Metabolic Disease
Metadata
Title
Treatment of extrapyramidal symptoms in a patient with homozygous homocystinuria
Authors
A. P. Burlina
C. Edini
A. B. Burlina
Publication date
01-05-2002
Publisher
Kluwer Academic Publishers
Published in
Journal of Inherited Metabolic Disease / Issue 2/2002
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1023/A:1015684912709

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3-Hydroxyglutarate excretion is increased in ketotic patients: Implications for glutaryl-CoA dehydrogenase deficiency testing

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A new case of CDG-x with stereotyped dystonic hand movements and optic atrophy

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Vitamin C therapy ameliorates vascular endothelial dysfunction in treated patients with homocystinuria

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Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: Outcome of treatment with amino acids
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Developed by: Springer Medicine

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