Παρακολούθηση
Dr Udo FH Engelke
Dr Udo FH Engelke
wetenschappelijk laboratoriummedewerker
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα labgk.umcn.nl
Τίτλος
Παρατίθεται από
Παρατίθεται από
Έτος
Next-generation metabolic screening: targeted and untargeted metabolomics for the diagnosis of inborn errors of metabolism in individual patients
KLM Coene, LAJ Kluijtmans, E van der Heeft, UFH Engelke, S de Boer, ...
Journal of inherited metabolic disease 41, 337-353, 2018
1672018
High-resolution 1H-NMR spectroscopy of blood plasma for metabolic studies
RA Wevers, U Engelke, A Heerschap
Clinical Chemistry 40 (7), 1245-1250, 1994
1541994
Proton nuclear magnetic resonance spectroscopy of body fluids in the field of inborn errors of metabolism
SH Moolenaar, UFH Engelke, RA Wevers
Annals of clinical biochemistry 40 (1), 16-24, 2003
1512003
NANS-mediated synthesis of sialic acid is required for brain and skeletal development
CDM Van Karnebeek, L Bonafé, XY Wen, M Tarailo-Graovac, S Balzano, ...
Nature Genetics 48 (7), 777-784, 2016
1482016
SUCNR1-mediated chemotaxis of macrophages aggravates obesity-induced inflammation and diabetes
JA van Diepen, JH Robben, GJ Hooiveld, C Carmone, M Alsady, ...
Diabetologia 60, 1304-1313, 2017
1442017
Standardized method for high-resolution 1H-NMR of cerebrospinal fluid
RA Wevers, U Engelke, U Wendel, JG De Jong, FJ Gabreels, ...
Clinical chemistry 41 (5), 744-751, 1995
1281995
Diagnosing inborn errors of lipid metabolism with proton nuclear magnetic resonance spectroscopy
M Oostendorp, UFH Engelke, MAAP Willemsen, RA Wevers
Clinical chemistry 52 (7), 1395-1405, 2006
1222006
The 3-methylglutaconic acidurias: what’s new?
SB Wortmann, LA Kluijtmans, UFH Engelke, RA Wevers, E Morava
Journal of inherited metabolic disease 35, 13-22, 2012
1122012
High‐resolution proton nuclear magnetic resonance spectroscopy of ovarian cyst fluid
EA Boss, SH Moolenaar, LFAG Massuger, H Boonstra, UFH Engelke, ...
NMR in Biomedicine: An International Journal Devoted to the Development and …, 2000
1122000
Dimethyl sulfone in human cerebrospinal fluid and blood plasma confirmed by one‐dimensional 1H and two‐dimensional 1H‐13C NMR
UFH Engelke, A Tangerman, MAAP Willemsen, D Moskau, S Loss, ...
NMR in Biomedicine 18 (5), 331-336, 2005
1112005
Biochemical and genetic analysis of 3-methylglutaconic aciduria type IV: a diagnostic strategy
SB Wortmann, RJT Rodenburg, A Jonckheere, MC De Vries, M Huizing, ...
Brain 132 (1), 136-146, 2009
1082009
1H-NMR Spectroscopy of Body Fluids: Inborn Errors of Purine and Pyrimidine Metabolism
RA Wevers, UFH Engelke, SH Moolenaar, C Brautigam, JGN de Jong, ...
Clinical chemistry 45 (4), 539-548, 1999
1061999
Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis
A Pol, GH Renkema, A Tangerman, EG Winkel, UF Engelke, ...
Nature genetics 50 (1), 120-129, 2018
982018
Leukoencephalopathy associated with a disturbance in the metabolism of polyols
MS Van der Knaap, RA Wevers, EA Struys, NM Verhoeven, PJW Pouwels, ...
Annals of neurology 46 (6), 925-928, 1999
951999
Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the …
S Wortmann, RJT Rodenburg, M Huizing, FJ Loupatty, T De Koning, ...
Molecular genetics and metabolism 88 (1), 47-52, 2006
852006
Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy study
SH Moolenaar, J Poggi-Bach, UFH Engelke, JMB Corstiaensen, ...
Clinical Chemistry 45 (4), 459-464, 1999
831999
A diagnostic biomarker profile for fibromyalgia syndrome based on an NMR metabolomics study of selected patients and controls
BG Malatji, H Meyer, S Mason, UFH Engelke, RA Wevers, M Van Reenen, ...
BMC neurology 17, 1-15, 2017
812017
Microbial metabolism shifts towards an adverse profile with supplementary iron in the TIM-2 in vitro model of the human colon
GAM Kortman, BE Dutilh, AJH Maathuis, KP Keegan, FGG Nielsen, ...
Frontiers in microbiology 6, 160740, 2016
812016
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism
JO Sass, V Mohr, H Olbrich, U Engelke, J Horvath, M Fliegauf, NT Loges, ...
The American Journal of Human Genetics 78 (3), 401-409, 2006
802006
Human ISPD is a cytidyltransferase required for dystroglycan O-mannosylation
M Riemersma, DS Froese, W van Tol, UF Engelke, J Kopec, ...
Chemistry & biology 22 (12), 1643-1652, 2015
782015
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