Marc Engelen
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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, 1-14, 2012
Adrenoleukodystrophy–neuroendocrine pathogenesis and redefinition of natural history
S Kemp, IC Huffnagel, GE Linthorst, RJ Wanders, M Engelen
Nature Reviews Endocrinology 12 (10), 606-615, 2016
Zellweger spectrum disorders: clinical overview and management approach
FCC Klouwer, K Berendse, S Ferdinandusse, RJA Wanders, M Engelen, ...
Orphanet journal of rare diseases 10, 1-11, 2015
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
X-linked adrenoleukodystrophy: pathogenesis and treatment
M Engelen, S Kemp, BT Poll-The
Current neurology and neuroscience reports 14, 1-8, 2014
The natural history of adrenal insufficiency in X-linked adrenoleukodystrophy: an international collaboration
IC Huffnagel, FK Laheji, R Aziz-Bose, NA Tritos, R Marino, GE Linthorst, ...
The Journal of Clinical Endocrinology & Metabolism 104 (1), 118-126, 2019
Thrombospondin-2 polymorphism is associated with a reduced risk of premature myocardial infarction
SM Boekholdt, MD Trip, RJG Peters, M Engelen, JMA Boer, EJM Feskens, ...
Arteriosclerosis, thrombosis, and vascular biology 22 (12), e24-e27, 2002
Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia
FM Vaz, JH McDermott, M Alders, SB Wortmann, S Kölker, ...
Brain 142 (11), 3382-3397, 2019
Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood
K Berendse, M Engelen, S Ferdinandusse, CBLM Majoie, HR Waterham, ...
Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2016
Frequent occurrence of cerebral demyelination in adrenomyeloneuropathy
M de Beer, M Engelen, BM van Geel
Neurology 83 (24), 2227-2231, 2014
Arterial spin labeling measurement of cerebral perfusion in children with sickle cell disease
S Gevers, AJ Nederveen, K Fijnvandraat, SM van den Berg, P van Ooij, ...
Journal of Magnetic Resonance Imaging 35 (4), 779-787, 2012
Volume of white matter hyperintensities is an independent predictor of intelligence quotient and processing speed in children with sickle cell disease
V van der Land, CT Hijmans, M de Ruiter, HJMM Mutsaerts, MH Cnossen, ...
British journal of haematology 168 (4), 553-556, 2015
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
MRF Reijnders, R Janowski, M Alvi, JE Self, TJ Van Essen, M Vreeburg, ...
Journal of medical genetics 55 (2), 104-113, 2018
Lovastatin in X-linked adrenoleukodystrophy
M Engelen, R Ofman, MGW Dijkgraaf, M Hijzen, LA van der Wardt, ...
New England Journal of Medicine 362 (3), 276-277, 2010
Disease progression in women with X-linked adrenoleukodystrophy is slow
IC Huffnagel, MGW Dijkgraaf, GE Janssens, M van Weeghel, ...
Orphanet Journal of Rare Diseases 14, 1-15, 2019
Effect of in vivo fetal infusion of dexamethasone at 0.75 GA on fetal ovine resistance artery responses to ET-1
CC Docherty, J Kalmar-Nagy, M Engelen, SV Koenen, M Nijland, RE Kuc, ...
American Journal of Physiology-Regulatory, Integrative and Comparative …, 2001
Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study
CL De Mol, YYM Wong, ED Van Pelt, IA Ketelslegers, DP Bakker, M Boon, ...
Journal of neurology 265, 1310-1319, 2018
Development of fetal vascular responses to endothelin-1 and acetylcholine in the sheep
CC Docherty, J Kalmar-Nagy, M Engelen, PW Nathanielsz
American Journal of Physiology-Regulatory, Integrative and Comparative …, 2001
Hematopoietic cell transplantation does not prevent myelopathy in X-linked adrenoleukodystrophy: a retrospective study
BM van Geel, BT Poll-The, A Verrips, JJ Boelens, S Kemp, M Engelen
Journal of inherited metabolic disease 38, 359-361, 2015
Comparison of C26: 0-carnitine and C26: 0-lysophosphatidylcholine as diagnostic markers in dried blood spots from newborns and patients with adrenoleukodystrophy
IC Huffnagel, MC van de Beek, AL Showers, JJ Orsini, FCC Klouwer, ...
Molecular genetics and metabolism 122 (4), 209-215, 2017
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