Engelke UF - Search Results

1

Hypoxia in fetal lambs: a study with (1)H-MNR spectroscopy of cerebrospinal fluid.

van Cappellen van Walsum AM, Jongsma HW, Wevers RA, Nijhuis JG, Crevels J, Engelke UF, Moolenaar SH, Oeseburg B, Nijland R. van Cappellen van Walsum AM, et al. Among authors: engelke uf. Pediatr Res. 2001 May;49(5):698-704. doi: 10.1203/00006450-200105000-00015. Pediatr Res. 2001. PMID: 11328955

2

Structural and functional analysis of ypt2, an essential ras-related gene in the fission yeast Schizosaccharomyces pombe encoding a Sec4 protein homologue.

Haubruck H, Engelke U, Mertins P, Gallwitz D. Haubruck H, et al. EMBO J. 1990 Jun;9(6):1957-62. doi: 10.1002/j.1460-2075.1990.tb08323.x. EMBO J. 1990. PMID: 2112089 Free PMC article.

3

MOGS-CDG: Quantitative analysis of the diagnostic Glc₃ Man tetrasaccharide and clinical spectrum of six new cases.

Post MA, de Wit I, Zijlstra FSM, Engelke UFH, van Rooij A, Christodoulou J, Tan TY, Le Fevre A, Jin D, Yaplito-Lee J, Lee BH, Low KJ, Mallick AA, Õunap K, Pitt J, Reardon W, Vals MA, Wortmann SB, Wessels HJCT, Bärenfänger M, van Karnebeek CDM, Lefeber DJ. Post MA, et al. Among authors: engelke ufh. J Inherit Metab Dis. 2023 Mar;46(2):313-325. doi: 10.1002/jimd.12588. Epub 2023 Feb 1. J Inherit Metab Dis. 2023. PMID: 36651519

4

Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy study.

Moolenaar SH, Poggi-Bach J, Engelke UF, Corstiaensen JM, Heerschap A, de Jong JG, Binzak BA, Vockley J, Wevers RA. Moolenaar SH, et al. Among authors: engelke uf. Clin Chem. 1999 Apr;45(4):459-64. Clin Chem. 1999. PMID: 10102904

5

1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolism.

Wevers RA, Engelke UF, Moolenaar SH, Bräutigam C, de Jong JG, Duran R, de Abreu RA, van Gennip AH. Wevers RA, et al. Among authors: engelke uf. Clin Chem. 1999 Apr;45(4):539-48. Clin Chem. 1999. PMID: 10102915

6

Leukoencephalopathy associated with a disturbance in the metabolism of polyols.

van der Knaap MS, Wevers RA, Struys EA, Verhoeven NM, Pouwels PJ, Engelke UF, Feikema W, Valk J, Jakobs C. van der Knaap MS, et al. Among authors: engelke uf. Ann Neurol. 1999 Dec;46(6):925-8. doi: 10.1002/1531-8249(199912)46:6<925::aid-ana18>3.0.co;2-j. Ann Neurol. 1999. PMID: 10589548

7

High-resolution proton nuclear magnetic resonance spectroscopy of ovarian cyst fluid.

Boss EA, Moolenaar SH, Massuger LF, Boonstra H, Engelke UF, de Jong JG, Wevers RA. Boss EA, et al. Among authors: engelke uf. NMR Biomed. 2000 Aug;13(5):297-305. doi: 10.1002/1099-1492(200008)13:5<297::aid-nbm648>3.0.co;2-i. NMR Biomed. 2000. PMID: 10960920

8

Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.

Binzak BA, Wevers RA, Moolenaar SH, Lee YM, Hwu WL, Poggi-Bach J, Engelke UF, Hoard HM, Vockley JG, Vockley J. Binzak BA, et al. Among authors: engelke uf. Am J Hum Genet. 2001 Apr;68(4):839-47. doi: 10.1086/319520. Epub 2001 Feb 28. Am J Hum Genet. 2001. PMID: 11231903 Free PMC article.

9

In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolism.

Moolenaar SH, van der Knaap MS, Engelke UF, Pouwels PJ, Janssen-Zijlstra FS, Verhoeven NM, Jakobs C, Wevers RA. Moolenaar SH, et al. Among authors: engelke uf. NMR Biomed. 2001 May;14(3):167-76. doi: 10.1002/nbm.690. NMR Biomed. 2001. PMID: 11357181

10

beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urine.

Moolenaar SH, Göhlich-Ratmann G, Engelke UF, Spraul M, Humpfer E, Dvortsak P, Voit T, Hoffmann GF, Bräutigam C, van Kuilenburg AB, van Gennip A, Vreken P, Wevers RA. Moolenaar SH, et al. Among authors: engelke uf. Magn Reson Med. 2001 Nov;46(5):1014-7. doi: 10.1002/mrm.1289. Magn Reson Med. 2001. PMID: 11675655 Free article.

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