Ron Wevers
Ron Wevers
Professor in Clinical Chemistry in Nijmegen
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα radboudumc.nl - Αρχική σελίδα
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The frequency of lysosomal storage diseases in The Netherlands
BJHM Poorthuis, RA Wevers, WJ Kleijer, JEM Groener, JGN de Jong, ...
Human genetics 105 (1-2), 151-156, 1999
7971999
Performance of near-infrared spectroscopy in measuring local O2 consumption and blood flow in skeletal muscle
MCP Van Beekvelt, WNJM Colier, RA Wevers, BGM Van Engelen
Journal of applied physiology 90 (2), 511-519, 2001
5542001
Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism
M Wyss, J Smeitink, RA Wevers, T Wallimann
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1102 (2), 119-166, 1992
4981992
Adipose tissue thickness affects in vivo quantitative near-IR spectroscopy in human skeletal muscle
MCP Van Beekvelt, MS Borghuis, BGM Van Engelen, RA Wevers, ...
Clinical science 101 (1), 21-28, 2001
3372001
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2
U Kornak, E Reynders, A Dimopoulou, J Van Reeuwijk, B Fischer, ...
Nature genetics 40 (1), 32-34, 2008
3282008
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder
WG Leen, J Klepper, MM Verbeek, M Leferink, T Hofste, BG van Engelen, ...
Brain 133 (3), 655-670, 2010
3262010
Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man
K Tuschl, PT Clayton, SM Gospe Jr, S Gulab, S Ibrahim, P Singhi, ...
The American Journal of Human Genetics 90 (3), 457-466, 2012
2552012
Role of cobalamin intake and atrophic gastritis in mild cobalamin deficiency in older Dutch subjects
DZ Van Asselt, LC de Groot, WA van Staveren, HJ Blom, RA Wevers, ...
The American journal of clinical nutrition 68 (2), 328-334, 1998
2491998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene
HR Waterham, FA Wijburg, RCM Hennekam, P Vreken, BT Poll-The, ...
The American Journal of Human Genetics 63 (2), 329-338, 1998
2491998
Elevated plasma chitotriosidase activity in various lysosomal storage disorders
Y Guo, W He, AM Boer, RA Wevers, AM De Bruijn, JEM Groener, ...
Journal of inherited metabolic disease 18 (6), 717-722, 1995
2491995
Dimethylmethylene blue-based spectrophotometry of glycosaminoglycans in untreated urine: a rapid screening procedure for mucopolysaccharidoses.
JG De Jong, RA Wevers, C Laarakkers, BJ Poorthuis
Clinical chemistry 35 (7), 1472-1477, 1989
2491989
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder
V Cantagrel, DJ Lefeber, BG Ng, Z Guan, JL Silhavy, SL Bielas, L Lehle, ...
Cell 142 (2), 203-217, 2010
2382010
Clinical and molecular characteristics associated with survival among patients treated with checkpoint inhibitors for advanced non–small cell lung carcinoma: a systematic …
CK Lee, J Man, S Lord, W Cooper, M Links, V Gebski, RS Herbst, ...
JAMA oncology 4 (2), 210-216, 2018
215*2018
Exome sequencing and the management of neurometabolic disorders
M Tarailo-Graovac, C Shyr, CJ Ross, GA Horvath, R Salvarinova, XC Ye, ...
New England Journal of Medicine 374 (23), 2246-2255, 2016
2092016
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness
R Carrozzo, C Dionisi-Vici, U Steuerwald, S Lucioli, F Deodato, ...
Brain 130 (3), 862-874, 2007
2032007
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis
A Verrips, LH Hoefsloot, GCH Steenbergen, JP Theelen, RA Wevers, ...
Brain 123 (5), 908-919, 2000
2002000
Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism
R Steinfeld, M Grapp, R Kraetzner, S Dreha-Kulaczewski, G Helms, ...
The American Journal of Human Genetics 85 (3), 354-363, 2009
1972009
Mechanisms in protein O-glycan biosynthesis and clinical and molecular aspects of protein O-glycan biosynthesis defects: a review
S Wopereis, DJ Lefeber, E Morava, RA Wevers
Clinical chemistry 52 (4), 574-600, 2006
1972006
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies
DJ Lefeber, J Schönberger, E Morava, M Guillard, KM Huyben, K Verrijp, ...
The American Journal of Human Genetics 85 (1), 76-86, 2009
1932009
Multiple phenotypes in phosphoglucomutase 1 deficiency
LC Tegtmeyer, S Rust, M van Scherpenzeel, BG Ng, ME Losfeld, S Timal, ...
New England Journal of Medicine 370 (6), 533-542, 2014
1922014
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