Stephan Kemp - Dissemin

Papers authored by Stephan Kemp

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2017 Irene C. Huffnagel, Malu-Clair van de Beek, Amanda L. Showers, Joseph J. Orsini, Femke C. C. Klouwer, Peter C. Schielen, Henk van Lenthe, Ronald J. A. Wanders, Frédéric M. Vaz, Mark A. Morrissey, Inge M. E. Dijkstra, Marc Engelen, Stephan Kemp

Comparison of C26:0-carnitine and C26:0-lysophosphatidylcholine as diagnostic markers in dried blood spots from newborns and patients with adrenoleukodystrophy

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Stephan Kemp

The Concise Guide To Pharmacology 2017/18

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Malu-Clair van de Beek, Rob Ofman, Inge Dijkstra, Frits Wijburg, Marc Engelen, Ronald Wanders, Stephan Kemp

Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophy

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Malu-Clair van de Beek, Inge M. E. Dijkstra, Stephan Kemp

Method for Measurement of Peroxisomal Very Long-Chain Fatty Acid Beta-Oxidation and De Novo C26:0 Synthesis Activity in Living Cells Using Stable-Isotope Labeled Docosanoic Acid

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2016 Catherine E. van Engen, Rob Ofman, Tessa Jacobs van Goethem, Eveline Verheij, Inge M. E. Dijkstra, Jennifer Varin, Michel Vidaud, Ronald J. A. Wanders, Patrick Aubourg, Stephan Kemp

, Mathieu Barbier

CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acids

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Gabor E. Linthorst, Ronald J. Wanders, Irene C. Huffnagel, Stephan Kemp

, Marc Engelen

Adrenoleukodystrophy – neuroendocrine pathogenesis and redefinition of natural history

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Martin J. A. Schackmann, Rob Ofman, Björn M. van Geel, Klaartje van Engelen, Ronald J. A. Wanders, Inge M. E. Dijkstra, Marc Engelen, Stephan Kemp

Pathogenicity of novel ABCD1 variants: The need for biochemical testing in the era of advanced genetics

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Malu-Clair van de Beek, Henk van Lenthe, Rob Ofman, Nicolas Schauer, Martin Schackmann, Frédéric M. Vaz, Wim Kulik, Ronald J. A. Wanders, Inge M. E. Dijkstra, Dalia Goldhaber-Pasillas, Joo-Yeon Engelen-Lee, Marc Engelen, Stephan Kemp

C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man

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2015 L. Potze, S. Di Franco, C. Grandela, M. L. Pras-Raves, D. I. Picavet, H. A. van Veen, H. van Lenthe, F. B. Mullauer, N. N. van der Wel, A. Luyf, A. H. C. van Kampen, S. Kemp

, V. Everts, J. H. Kessler, F. M. Vaz and 1 other authors

Betulinic acid induces a novel cell death pathway that depends on cardiolipin modification

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Martin J. A. Schackmann, Rob Ofman, Inge M. E. Dijkstra, Ronald J. A. Wanders, Stephan Kemp

Enzymatic characterization of ELOVL1, a key enzyme in very long-chain fatty acid synthesis

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2014 Björn M. van Geel, Bwee Tien Poll-The, Aad Verrips, Jaap-Jan Boelens, Stephan Kemp

, Marc Engelen

Hematopoietic cell transplantation does not prevent myelopathy in X-linked adrenoleukodystrophy: a retrospective study

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Marc Engelen, Mathieu Barbier, Inge M. E. Dijkstra, Remmelt Schür

, Rob M. A. Camiel Verhamme, Camiel Verhamme, Marcel G. W. Dijkgraaf, Patrick A. Aubourg, Ronald J. A. Wanders, Bjorn M. van Geel, Marianne de Visser, M. de Visser, Bwee T. Poll The, Stephan Kemp

Reply: Age-dependent penetrance among females with X-linked adrenoleukodystrophy

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Marc Engelen, Stephan Kemp

, Bwee-Tien Poll-The

X-Linked Adrenoleukodystrophy: Pathogenesis and Treatment

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Marc Engelen, Mathieu Barbier, Inge M. E. Dijkstra, Remmelt Schür

, Rob M. A. de Bie, Camiel Verhamme, Marcel G. W. Dijkgraaf, Patrick A. Aubourg, Ronald J. A. Wanders, Bjorn M. van Geel, Marianne de Visser, Bwee T. Poll The, Stephan Kemp

X-linked adrenoleukodystrophy in women: A cross-sectional cohort study

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2013 Marc Engelen, Rob Ofman, Marcel Dijkgraaf, Bjorn van Geel, Marianne de Visser, Ronald Wanders, Bwee Tien Poll-The, Stephan Kemp

Comment on the paper “Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: A revisit”

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Daniela Q. C. M. Barge‐Schaapveld, Rob Ofman, Alida C. Knegt, Mariëlle Alders, Wolfgang Höhne, Stephan Kemp

, Raoul C. M. Hennekam

Intellectual Disability and Hemizygous GPD2 Mutation

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2012 Cyntia Anabel Amorosi, Helena Myskóva, Mariela Roxana Monti, Carlos Enrique Argaraña, Masashi Morita, Stephan Kemp

, Raquel Dodelson de Kremer, Lenka Dvoráková, Ana María Oller de Ramírez

X-Linked Adrenoleukodystrophy: Molecular and Functional Analysis of the ABCD1 Gene in Argentinean Patients

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Stephan Kemp

, Johannes Berger, Patrick Aubourg

X-linked adrenoleukodystrophy: Clinical, metabolic, genetic and pathophysiological aspects

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Marc Engelen, Luc Tran, Rob Ofman, Josephine Brennecke, Ann B. Moser, Inge M. E. Dijkstra, Ronald J. A. Wanders, Bwee Tien Poll-The, Stephan Kemp

Bezafibrate for X-Linked Adrenoleukodystrophy

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Merel S. Ebberink, Janet Koster, Gepke Visser, Francjan van Spronsen, Irene Stolte-Dijkstra, G. Peter A. Smit, Johanna M. Fock, Stephan Kemp

, Ronald J. A. Wanders, Hans R. Waterham

A novel defect of peroxisome division due to a homozygous non-sense mutation in thePEX11βgene

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Papers authored by Stephan Kemp