Moolenaar SH - Search Results

1

1H-NMR spectroscopy of cerebrospinal fluid of fetal sheep during hypoxia-induced acidemia and recovery.

Van Cappellen Van Walsum AM, Jongsma HW, Wevers RA, Nijhuis JG, Crevels J, Engelke UF, De Abreu RA, Moolenaar SH, Oeseburg B, Nijland R. Van Cappellen Van Walsum AM, et al. Among authors: moolenaar sh. Pediatr Res. 2002 Jul;52(1):56-63. doi: 10.1203/00006450-200207000-00012. Pediatr Res. 2002. PMID: 12084848

2

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: moolenaar sh. Pediatr Res. 2001 May;49(5):698-704. doi: 10.1203/00006450-200105000-00015. Pediatr Res. 2001. PMID: 11328955

3

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: moolenaar sh. Clin Chem. 1999 Apr;45(4):539-48. Clin Chem. 1999. PMID: 10102915

4

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: moolenaar sh. 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

5

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. NMR Biomed. 2001 May;14(3):167-76. doi: 10.1002/nbm.690. NMR Biomed. 2001. PMID: 11357181

6

Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine.

Moolenaar SH, Engelke UF, Abeling NG, Mandel H, Duran M, Wevers RA. Moolenaar SH, et al. J Inherit Metab Dis. 2001 Dec;24(8):843-50. doi: 10.1023/a:1013940207973. J Inherit Metab Dis. 2001. PMID: 11916317

7

Proton nuclear magnetic resonance spectroscopy of body fluids in the field of inborn errors of metabolism.

Moolenaar SH, Engelke UF, Wevers RA. Moolenaar SH, et al. Ann Clin Biochem. 2003 Jan;40(Pt 1):16-24. doi: 10.1258/000456303321016132. Ann Clin Biochem. 2003. PMID: 12542907 Review.

8

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. Clin Chem. 1999 Apr;45(4):459-64. Clin Chem. 1999. PMID: 10102904

9

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. Magn Reson Med. 2001 Nov;46(5):1014-7. doi: 10.1002/mrm.1289. Magn Reson Med. 2001. PMID: 11675655 Free article.

10

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: moolenaar sh. 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.

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