Hagenfeldt L - Search Results

1

Vigabatrin therapy in six patients with succinic semialdehyde dehydrogenase deficiency.

Gibson KM, Jakobs C, Ogier H, Hagenfeldt L, Eeg-Olofsson KE, Eeg-Olofsson O, Aksu F, Weber HP, Rossier E, Vollmer B, et al. Gibson KM, et al. Among authors: hagenfeldt l. J Inherit Metab Dis. 1995;18(2):143-6. doi: 10.1007/BF00711750. J Inherit Metab Dis. 1995. PMID: 7564230 No abstract available.

2

D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boy.

Eeg-Olofsson O, Zhang WW, Olsson Y, Jagell S, Hagenfeldt L. Eeg-Olofsson O, et al. Among authors: hagenfeldt l. J Child Neurol. 2000 Jul;15(7):488-92. doi: 10.1177/088307380001500714. J Child Neurol. 2000. PMID: 10921524

3

Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Hagenfeldt L, Venizelos N, von Döbeln U. Hagenfeldt L, et al. J Inherit Metab Dis. 1995;18(2):245-8. doi: 10.1007/BF00711779. J Inherit Metab Dis. 1995. PMID: 7564259 No abstract available.

4

N-acetylaspartic aciduria due to aspartoacylase deficiency--a new aetiology of childhood leukodystrophy.

Hagenfeldt L, Bollgren I, Venizelos N. Hagenfeldt L, et al. J Inherit Metab Dis. 1987;10(2):135-41. doi: 10.1007/BF01800038. J Inherit Metab Dis. 1987. PMID: 3116332

5

Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency.

von Döbeln U, Venizelos N, Westgren M, Hagenfeldt L. von Döbeln U, et al. Among authors: hagenfeldt l. J Inherit Metab Dis. 1994;17(2):185-8. doi: 10.1007/BF00711615. J Inherit Metab Dis. 1994. PMID: 7967472

6

5-Oxoprolinuria (glutathione synthetase deficiency): a case with neonatal presentation and rapid fatal outcome.

Divry P, Roulaud-Parrot F, Dorche C, Zabot MT, Contraire B, Hagenfeldt L, Larsson A. Divry P, et al. Among authors: hagenfeldt l. J Inherit Metab Dis. 1991;14(3):341-4. doi: 10.1007/BF01811698. J Inherit Metab Dis. 1991. PMID: 1770788 No abstract available.

7

Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples.

von Döbeln U, Venizelos N, Hagenfeldt L. von Döbeln U, et al. Among authors: hagenfeldt l. J Inherit Metab Dis. 1990;13(2):165-8. doi: 10.1007/BF01799680. J Inherit Metab Dis. 1990. PMID: 2143242

8

Fatty acid oxidation in fibroblasts from patients with defects in beta-oxidation and in the respiratory chain.

Venizelos N, von Döbeln U, Hagenfeldt L. Venizelos N, et al. Among authors: hagenfeldt l. J Inherit Metab Dis. 1998 Jun;21(4):409-15. doi: 10.1023/a:1005310809714. J Inherit Metab Dis. 1998. PMID: 9700598

9

beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduria.

Venizelos N, Ijlst L, Wanders RJ, Hagenfeldt L. Venizelos N, et al. Among authors: hagenfeldt l. Pediatr Res. 1994 Jul;36(1 Pt 1):111-4. doi: 10.1203/00006450-199407001-00020. Pediatr Res. 1994. PMID: 7936829 Clinical Trial.

10

Prevalence of the 985A>G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden.

Johansson A, Guthenberg C, Ahlman H, Von Döbeln U, Hagenfeldt L. Johansson A, et al. Among authors: hagenfeldt l. Scand J Clin Lab Invest. 1999 Jul;59(4):289-91. doi: 10.1080/00365519950185652. Scand J Clin Lab Invest. 1999. PMID: 10463467

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