Instructions to Authors.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 319, doi. 10.1023/A:1024424905709
- Publication type:
- Article
Works matching IS 01418955 AND DT 2003 AND VI 26 AND IP 2/3
Results: 18
1
2
X-linked creatine transporter defect: An overview.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 309, doi. 10.1023/A:1024405821638
- By:
- Publication type:
- Article
3
Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 299, doi. 10.1023/A:1024453704800
- By:
- Publication type:
- Article
4
Choices for treatment of hyperlipidaemia.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 289, doi. 10.1023/A:1024401720730
- By:
- Publication type:
- Article
5
Lipoprotein disorders and cardiovascular risk.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 267, doi. 10.1023/A:1024449603891
- By:
- Publication type:
- Article
6
Classical homocystinuria: Vascular risk and its prevention.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 259, doi. 10.1023/A:1024497419821
- By:
- Publication type:
- Article
7
Overview of inherited metabolic disorders causing cardiovascular disease.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 245, doi. 10.1023/A:1024445402983
- By:
- Publication type:
- Article
8
The eye as a window to inborn errors of metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 229, doi. 10.1023/A:1024493318913
- By:
- Publication type:
- Article
9
A review of primary hereditary optic neuropathies.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 209, doi. 10.1023/A:1024441302074
- By:
- Publication type:
- Article
10
Mitochondrial disorders: Clinical presentation and diagnostic dilemmas.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 199, doi. 10.1023/A:1024489218004
- By:
- Publication type:
- Article
11
Mitochondrial oxidative phosphorylation: Pitfalls and tips in measuring and interpreting enzyme activities.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 189, doi. 10.1023/A:1024437201166
- By:
- Publication type:
- Article
12
L-Carnitine in inborn errors of metabolism: What is the evidence?
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 181, doi. 10.1023/A:1024485117095
- By:
- Publication type:
- Article
13
Treatment of carnitine deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 171, doi. 10.1023/A:1024433100257
- By:
- Publication type:
- Article
14
Carnitine transport: Pathophysiology and metabolism of known molecular defects.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 147, doi. 10.1023/A:1024481016187
- By:
- Publication type:
- Article
15
Diagnosis of inherited disorders of liver metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 135, doi. 10.1023/A:1024429032116
- By:
- Publication type:
- Article
16
Mass spectrometric analysis of glycans in elucidating the pathogenesis of CDG type IIx.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 119, doi. 10.1023/A:1024476915278
- By:
- Publication type:
- Article
17
Congenital disorders of glycosylation (CDG): It's all in it!
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 99, doi. 10.1023/A:1024431131208
- By:
- Publication type:
- Article
18
Preface.
- Published in:
- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 2/3, p. 97, doi. 10.1023/A:1024468314369
- Publication type:
- Article