Kemp S - Search Results

1

X-linked adrenoleukodystrophy: pathogenesis and treatment.

Engelen M, Kemp S, Poll-The BT. Engelen M, et al. Among authors: kemp s. Curr Neurol Neurosci Rep. 2014 Oct;14(10):486. doi: 10.1007/s11910-014-0486-0. Curr Neurol Neurosci Rep. 2014. PMID: 25115486 Review.

2

Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations.

Kemp S, Ligtenberg MJ, van Geel BM, Barth PG, Wolterman RA, Schoute F, Sarde CO, Mandel JL, van Oost BA, Bolhuis PA. Kemp S, et al. Biochem Biophys Res Commun. 1994 Jul 29;202(2):647-53. doi: 10.1006/bbrc.1994.1979. Biochem Biophys Res Commun. 1994. PMID: 8048932

3

Two intronic mutations in the adrenoleukodystrophy gene.

Kemp S, Ligtenberg MJ, van Geel BM, Barth PG, Sarde CO, van Oost BA, Bolhuis PA. Kemp S, et al. Hum Mutat. 1995;6(3):272-3. doi: 10.1002/humu.1380060316. Hum Mutat. 1995. PMID: 8535452 No abstract available.

4

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

Kemp S, Mooyer PA, Bolhuis PA, van Geel BM, Mandel JL, Barth PG, Aubourg P, Wanders RJ. Kemp S, et al. J Inherit Metab Dis. 1996;19(5):667-74. doi: 10.1007/BF01799844. J Inherit Metab Dis. 1996. PMID: 8892025

5

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.

Kemp S, Pujol A, Waterham HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. Kemp S, et al. Hum Mutat. 2001 Dec;18(6):499-515. doi: 10.1002/humu.1227. Hum Mutat. 2001. PMID: 11748843 Review.

6

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. Kemp S, et al. Mol Genet Metab. 2005 Feb;84(2):144-51. doi: 10.1016/j.ymgme.2004.09.015. Mol Genet Metab. 2005. PMID: 15670720

7

Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy.

Linnebank M, Kemp S, Wanders RJ, Kleijer WJ, van der Sterre ML, Gärtner J, Fliessbach K, Semmler A, Sokolowski P, Köhler W, Schlegel U, Schmidt S, Klockgether T, Wüllner U. Linnebank M, et al. Among authors: kemp s. Neurology. 2006 Feb 14;66(3):442-3. doi: 10.1212/01.wnl.0000196491.42058.6f. Neurology. 2006. PMID: 16476952

8

Omega-oxidation of very long-chain fatty acids in human liver microsomes. Implications for X-linked adrenoleukodystrophy.

Sanders RJ, Ofman R, Duran M, Kemp S, Wanders RJA. Sanders RJ, et al. Among authors: kemp s. J Biol Chem. 2006 May 12;281(19):13180-13187. doi: 10.1074/jbc.M513481200. Epub 2006 Mar 17. J Biol Chem. 2006. PMID: 16547005 Free article.

9

The peroxisomal ABC transporter family.

Wanders RJ, Visser WF, van Roermund CW, Kemp S, Waterham HR. Wanders RJ, et al. Among authors: kemp s. Pflugers Arch. 2007 Feb;453(5):719-34. doi: 10.1007/s00424-006-0142-x. Epub 2006 Oct 13. Pflugers Arch. 2007. PMID: 17039367 Review.

10

X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment.

Kemp S, Wanders RJ. Kemp S, et al. Mol Genet Metab. 2007 Mar;90(3):268-76. doi: 10.1016/j.ymgme.2006.10.001. Epub 2006 Nov 7. Mol Genet Metab. 2007. PMID: 17092750 Review.

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