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Similar articles for PubMed (Select 7845889)

1.

Pitfalls in the prenatal diagnosis of peroxisomal beta-oxidation defects by chorionic villus sampling.

Carey WF, Poulos A, Sharp P, Nelson PV, Robertson EF, Hughes JL, Gill A.

Prenat Diagn. 1994 Sep;14(9):813-9.

PMID:
7845889
2.

A misdiagnosis of X-linked adrenoleukodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acids.

Gray RG, Green A, Cole T, Davidson V, Giles M, Schutgens RB, Wanders RJ.

Prenat Diagn. 1995 May;15(5):486-90.

PMID:
7644440
4.

Prenatal diagnosis of inborn errors in peroxisomal beta-oxidation.

Wanders RJ, Schutgens RB, van den Bosch H, Tager JM, Kleijer WJ.

Prenat Diagn. 1991 Apr;11(4):253-61.

PMID:
1896411
5.

Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.

Wanders RJ, van Roermund CW, van Wijland MJ, Heikoop J, Schutgens RB, Schram AW, Tager JM, van den Bosch H, Poll-Thé BT, Saudubray JM, et al.

Clin Chim Acta. 1987 Jul 15;166(2-3):255-63.

PMID:
2441904
6.

X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.

Wanders RJ, van Roermund CW, van Wijland MJ, Nijenhuis AA, Tromp A, Schutgens RB, Brouwer-Kelder EM, Schram AW, Tager JM, van den Bosch H, et al.

Clin Chim Acta. 1987 Jun 15;165(2-3):321-9.

PMID:
3652454
8.

Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders.

Wanders RJ, van Wijland MJ, van Roermund CW, Schutgens RB, van den Bosch H, Tager JM, Nijenhuis A, Tromp A.

Clin Chim Acta. 1987 Jun 15;165(2-3):303-10.

PMID:
3652452
10.

[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment].

Wanders RJ, Barth PG, Schutgens RB, Van den Bosch H, Tager JM, Stroink H, Przyrembel H, Heymans HS.

Tijdschr Kindergeneeskd. 1989 Oct;57(5):186-97. Review. Dutch.

PMID:
2683204
11.

ALDP expression in fetal cells and its application in prenatal diagnosis of X-linked adrenoleukodystrophy.

Ruiz M, Coll MJ, Pampols T, Girós M.

Prenat Diagn. 1997 Jul;17(7):651-6.

PMID:
9249866
12.
13.

[Screening for carrier and prenatal diagnosis of X-linked adrenoleukodystrophy].

Wang AH, Bao XH, Xiong H, Pan H, Wu Y, Zhang YH, Shi CY, Qin J, Wu XR.

Zhonghua Er Ke Za Zhi. 2005 May;43(5):345-9. Chinese.

PMID:
15924749
14.

Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy.

Kemp S, Valianpour F, Denis S, Ofman R, Sanders RJ, Mooyer P, Barth PG, Wanders RJ.

Mol Genet Metab. 2005 Feb;84(2):144-51. Erratum in: Mol Genet Metab. 2008 Mar;93(3):350.

PMID:
15670720
15.

Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy.

McGuinness MC, Zhang HP, Smith KD.

Mol Genet Metab. 2001 Sep-Oct;74(1-2):256-63.

PMID:
11592822
16.

Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins.

Braiterman LT, Zheng S, Watkins PA, Geraghty MT, Johnson G, McGuinness MC, Moser AB, Smith KD.

Hum Mol Genet. 1998 Feb;7(2):239-47.

17.
18.

Very long-chain fatty acids in peroxisomal disease.

Poulos A, Beckman K, Johnson DW, Paton BC, Robinson BS, Sharp P, Usher S, Singh H.

Adv Exp Med Biol. 1992;318:331-40.

PMID:
1378993
19.

First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe.

Boué J, Oberle I, Heilig R, Mandel JL, Moser A, Moser H, Larsen JW Jr, Dumez Y, Boué A.

Hum Genet. 1985;69(3):272-4.

PMID:
3856557
20.
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