PPARs as therapeutic targets for correction of inborn mitochondrial fatty acid oxidation disorders.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 217, doi. 10.1007/s10545-008-0844-7
- By:
- Publication type:
- Article
Works matching IS 01418955 AND DT 2008 AND VI 31 AND IP 2
Results: 16
1
2
Congenital disorders of glycosylation—a challenging group of IEMs.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 267, doi. 10.1007/s10545-008-0849-2
- By:
- Publication type:
- Article
3
AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: A review.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 230, doi. 10.1007/s10545-008-0826-9
- By:
- Publication type:
- Article
4
Sanfilippo syndrome: A mini-review.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 240, doi. 10.1007/s10545-008-0838-5
- By:
- Publication type:
- Article
5
Disorders caused by deficiency of succinate-CoA ligase.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 226, doi. 10.1007/s10545-008-0828-7
- By:
- Publication type:
- Article
6
Liver cell transplantation for the treatment of inborn errors of metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 164, doi. 10.1007/s10545-008-0829-6
- By:
- Publication type:
- Article
7
Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: A review.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 205, doi. 10.1007/s10545-008-0841-x
- By:
- Publication type:
- Article
8
Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia—A new metabolic disorder.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 151, doi. 10.1007/s10545-008-0813-1
- By:
- Publication type:
- Article
9
The consequences of extended newborn screening programmes: Do we know who needs treatment?
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 173, doi. 10.1007/s10545-008-0843-8
- By:
- Publication type:
- Article
10
Molecular physiology and pathophysiology of lysosomal membrane transporters.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 258, doi. 10.1007/s10545-008-0879-9
- By:
- Publication type:
- Article
11
Molecular analysis of the GlcNac-1-phosphotransferase.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 253, doi. 10.1007/s10545-008-0862-5
- By:
- Publication type:
- Article
12
Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patients.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 270, doi. 10.1007/s10545-008-0856-3
- By:
- Publication type:
- Article
13
Inherited epithelial transporter disorders—an overview.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 178, doi. 10.1007/s10545-008-0861-6
- By:
- Publication type:
- Article
14
Apoprotein A-V: An important regulator of triglyceride metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 281, doi. 10.1007/s10545-008-0863-4
- By:
- Publication type:
- Article
15
Membrane translocation of glutaric acid and its derivatives.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 188, doi. 10.1007/s10545-008-0825-x
- By:
- Publication type:
- Article
16
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 194, doi. 10.1007/s10545-008-0823-z
- By:
- Publication type:
- Article