Stephan Kemp
Stephan Kemp
Amsterdam University Medical Centers, the Netherlands
Verified email at amsterdamumc.nl - Homepage
Title
Cited by
Cited by
Year
Histone deacetylases (HDACs): characterization of the classical HDAC family
AJM Ruijter, AH GENNIP, HN Caron, S Kemp, ABP KUILENBURG
Biochemical Journal 370 (3), 737-749, 2003
32582003
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
M Engelen, S Kemp, M De Visser, BM van Geel, RJA Wanders, ...
Orphanet journal of rare diseases 7 (1), 1-14, 2012
3252012
ABCD1 mutations and the X‐linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations
S Kemp, A Pujol, HR Waterham, BM Van Geel, CD Boehm, GV Raymond, ...
Human mutation 18 (6), 499-515, 2001
2892001
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy
S Kemp, HM Wei, JF Lu, LT Braiterman, MC McGuinness, AB Moser, ...
Nature medicine 4 (11), 1261-1268, 1998
2731998
The concise guide to pharmacology 2017/18: overview
SPH Alexander, E Kelly, NV Marrion, JA Peters, E Faccenda, SD Harding, ...
British journal of pharmacology 174, S1-S16, 2017
2442017
N-glycosylation and deletion mutants of the human MDR1 P-glycoprotein.
AH Schinkel, S Kemp, M Dolle, G Rudenko, E Wagenaar
Journal of Biological Chemistry 268 (10), 7474-7481, 1993
2401993
Deletion of the serine 34 codon from the major peripheral myelin protein P 0 gene in Charcot–Marie–Tooth disease type 1B
T Kulkens, PA Bolhuis, RA Wolterman, S Kemp, S te Nijenhuis, ...
Nature genetics 5 (1), 35-39, 1993
2261993
X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects
S Kemp, J Berger, P Aubourg
Biochimica Et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (9 …, 2012
2192012
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes
KD Smith, S Kemp, LT Braiterman, JF Lu, HM Wei, M Geraghty, G Stetten, ...
Neurochemical research 24 (4), 521-535, 1999
2041999
Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy
S Fourcade, J Lopez-Erauskin, J Galino, C Duval, A Naudi, M Jove, ...
Human molecular genetics 17 (12), 1762-1773, 2008
1902008
Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome
MA Fath, RF Mullins, C Searby, DY Nishimura, J Wei, K Rahmouni, ...
Human molecular genetics 14 (9), 1109-1118, 2005
1862005
Peroxisomes, lipid metabolism and lipotoxicity
RJA Wanders, S Ferdinandusse, P Brites, S Kemp
Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2010
1802010
Fatty acid omega‐oxidation as a rescue pathway for fatty acid oxidation disorders in humans
RJA Wanders, J Komen, S Kemp
The FEBS journal 278 (2), 182-194, 2011
1772011
Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry
F Valianpour, JJM Selhorst, LEM van Lint, AH van Gennip, RJA Wanders, ...
Molecular genetics and metabolism 79 (3), 189-196, 2003
1362003
The role of ELOVL1 in very long‐chain fatty acid homeostasis and X‐linked adrenoleukodystrophy
R Ofman, IME Dijkstra, CWT van Roermund, N Burger, M Turkenburg, ...
EMBO molecular medicine 2 (3), 90-97, 2010
1352010
Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein.
MJ Ligtenberg, S Kemp, CO Sarde, BM van Geel, WJ Kleijer, PG Barth, ...
American journal of human genetics 56 (1), 44, 1995
1321995
X-linked adrenoleukodystrophy in women: a cross-sectional cohort study
M Engelen, M Barbier, IME Dijkstra, R Schür, RMA de Bie, C Verhamme, ...
Brain 137 (3), 693-706, 2014
1292014
The peroxisomal ABC transporter family
RJA Wanders, WF Visser, CWT van Roermund, S Kemp, HR Waterham
Pflügers Archiv-European Journal of Physiology 453 (5), 719-734, 2007
1232007
A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene
MS Ebberink, J Koster, G Visser, F van Spronsen, I Stolte-Dijkstra, ...
Journal of medical genetics 49 (5), 307-313, 2012
1212012
Adrenoleukodystrophy–neuroendocrine pathogenesis and redefinition of natural history
S Kemp, IC Huffnagel, GE Linthorst, RJ Wanders, M Engelen
Nature Reviews Endocrinology 12 (10), 606, 2016
1202016
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