Vreken P - Search Results

1

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060).

Barth PG, Wanders RJ, Vreken P, Janssen EA, Lam J, Baas F. Barth PG, et al. Among authors: vreken p. J Inherit Metab Dis. 1999 Jun;22(4):555-67. doi: 10.1023/a:1005568609936. J Inherit Metab Dis. 1999. PMID: 10407787 Review.

2

Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts.

Valianpour F, Wanders RJ, Overmars H, Vreken P, Van Gennip AH, Baas F, Plecko B, Santer R, Becker K, Barth PG. Valianpour F, et al. Among authors: vreken p. J Pediatr. 2002 Nov;141(5):729-33. doi: 10.1067/mpd.2002.129174. J Pediatr. 2002. PMID: 12410207

3

L-2-hydroxyglutaric aciduria and lactic acidosis.

Barth PG, Wanders RJ, Scholte HR, Abeling N, Jakobs C, Schutgens RB, Vreken P. Barth PG, et al. Among authors: vreken p. J Inherit Metab Dis. 1998 Jun;21(3):251-4. doi: 10.1023/a:1005316121584. J Inherit Metab Dis. 1998. PMID: 9686369 No abstract available.

4

X-linked adrenoleukodystrophy: improved prenatal diagnosis using both biochemical and immunological methods.

Wanders RJ, Mooyer PW, Dekker C, Vreken P. Wanders RJ, et al. Among authors: vreken p. J Inherit Metab Dis. 1998 Jun;21(3):285-7. doi: 10.1023/a:1005336726127. J Inherit Metab Dis. 1998. PMID: 9686376 No abstract available.

5

Analysis of plasmenylethanolamines using electrospray tandem mass spectrometry and its application in screening for peroxisomal disorders.

Vreken P, Valianpour F, Overmars H, Barth PG, Selhorst JJ, van Gennip AH, Wanders RJ. Vreken P, et al. J Inherit Metab Dis. 2000 Jun;23(4):429-33. doi: 10.1023/a:1005676507682. J Inherit Metab Dis. 2000. PMID: 10896311 No abstract available.

6

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome.

Vreken P, Valianpour F, Nijtmans LG, Grivell LA, Plecko B, Wanders RJ, Barth PG. Vreken P, et al. Biochem Biophys Res Commun. 2000 Dec 20;279(2):378-82. doi: 10.1006/bbrc.2000.3952. Biochem Biophys Res Commun. 2000. PMID: 11118295

7

Quantitative plasma acylcarnitine analysis using electrospray tandem mass spectrometry for the diagnosis of organic acidaemias and fatty acid oxidation defects.

Vreken P, van Lint AE, Bootsma AH, Overmars H, Wanders RJ, van Gennip AH. Vreken P, et al. J Inherit Metab Dis. 1999 May;22(3):302-6. doi: 10.1023/a:1005587617745. J Inherit Metab Dis. 1999. PMID: 10384392 No abstract available.

8

Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: application for selective screening of peroxisomal disorders.

Bootsma AH, Overmars H, van Rooij A, van Lint AE, Wanders RJ, van Gennip AH, Vreken P. Bootsma AH, et al. Among authors: vreken p. J Inherit Metab Dis. 1999 May;22(3):307-10. doi: 10.1023/a:1005543802724. J Inherit Metab Dis. 1999. PMID: 10384393 No abstract available.

9

Disorders of mitochondrial fatty acyl-CoA beta-oxidation.

Wanders RJ, Vreken P, den Boer ME, Wijburg FA, van Gennip AH, IJlst L. Wanders RJ, et al. Among authors: vreken p. J Inherit Metab Dis. 1999 Jun;22(4):442-87. doi: 10.1023/a:1005504223140. J Inherit Metab Dis. 1999. PMID: 10407780 Review.

10

Spontaneous pregnancy in a patient with classical galactosaemia.

de Jongh S, Vreken P, IJst L, Wanders RJ, Jakobs C, Bakker HD. de Jongh S, et al. Among authors: vreken p. J Inherit Metab Dis. 1999 Aug;22(6):754-5. doi: 10.1023/a:1005504403173. J Inherit Metab Dis. 1999. PMID: 10472536 No abstract available.

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