van Gennip AH - Search Results

1

Monoamine oxidase A deficiency: biogenic amine metabolites in random urine samples.

Abeling NG, van Gennip AH, van Cruchten AG, Overmars H, Brunner HG. Abeling NG, et al. Among authors: van gennip ah, van cruchten ag. J Neural Transm Suppl. 1998;52:9-15. doi: 10.1007/978-3-7091-6499-0_2. J Neural Transm Suppl. 1998. PMID: 9564603

2

Biogenic amine metabolite patterns in the urine of monoamine oxidase A-deficient patients. A possible tool for diagnosis.

Abeling NG, van Gennip AH, Overmars H, van Oost BA, Brunner HG. Abeling NG, et al. Among authors: van gennip ah, van oost ba. J Inherit Metab Dis. 1994;17(3):339-41. doi: 10.1007/BF00711824. J Inherit Metab Dis. 1994. PMID: 7807947 Clinical Trial. No abstract available.

3

The detection of molybdenum cofactor deficiency: clinical symptomatology and urinary metabolite profile.

van Gennip AH, Abeling NG, Stroomer AE, Overmars H, Bakker HD. van Gennip AH, et al. J Inherit Metab Dis. 1994;17(1):142-5. doi: 10.1007/BF00735420. J Inherit Metab Dis. 1994. PMID: 8051926 No abstract available.

4

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.

Brunner HG, Nelen MR, van Zandvoort P, Abeling NG, van Gennip AH, Wolters EC, Kuiper MA, Ropers HH, van Oost BA. Brunner HG, et al. Among authors: van gennip ah, van oost ba, van zandvoort p. Am J Hum Genet. 1993 Jun;52(6):1032-9. Am J Hum Genet. 1993. PMID: 8503438 Free PMC article.

5

Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.

Lenders JW, Eisenhofer G, Abeling NG, Berger W, Murphy DL, Konings CH, Wagemakers LM, Kopin IJ, Karoum F, van Gennip AH, Brunner HG. Lenders JW, et al. Among authors: van gennip ah. J Clin Invest. 1996 Feb 15;97(4):1010-9. doi: 10.1172/JCI118492. J Clin Invest. 1996. PMID: 8613523 Free PMC article.

6

Aromatic L-amino acid decarboxylase deficiency: a new case with a mild clinical presentation and unexpected laboratory findings.

Abeling NG, van Gennip AH, Barth PG, van Cruchten A, Westra M, Wijburg FA. Abeling NG, et al. Among authors: van gennip ah, van cruchten a. J Inherit Metab Dis. 1998 Jun;21(3):240-2. doi: 10.1023/a:1005307919767. J Inherit Metab Dis. 1998. PMID: 9686366 No abstract available.

7

High-performance liquid chromatographic analysis of biogenic amines in cells and in culture media using on-line dialysis and trace enrichment.

Slingerland RJ, Van Kuilenburg AB, Bodlaender JM, Overmars H, Voûte PA, Van Gennip AH. Slingerland RJ, et al. Among authors: van gennip ah, van kuilenburg ab. J Chromatogr B Biomed Sci Appl. 1998 Sep 25;716(1-2):65-75. doi: 10.1016/s0378-4347(98)00267-9. J Chromatogr B Biomed Sci Appl. 1998. PMID: 9824219

8

Mild learning difficulties and offending behaviour--is there a link with monoamine oxidase A deficiency?

Stamps VR, Abeling NG, van Gennip AH, van Cruchten AG, Gurling HM. Stamps VR, et al. Among authors: van gennip ah, van cruchten ag. Psychiatr Genet. 2001 Sep;11(3):173-6. doi: 10.1097/00041444-200109000-00012. Psychiatr Genet. 2001. PMID: 11702062

9

Simultaneous determination of acidic 3,4-dihydroxyphenylalanine metabolites and 5-hydroxyindole-3-acetic acid in urine by high-performance liquid chromatography.

Stroomer AE, Overmars H, Abeling NG, van Gennip AH. Stroomer AE, et al. Among authors: van gennip ah. Clin Chem. 1990 Oct;36(10):1834-7. Clin Chem. 1990. PMID: 1698577

10

Diagnosis of a new case of trimethylaminuria using direct proton NMR spectroscopy of urine.

Abeling NG, van Gennip AH, Bakker HD, Heerschap A, Engelke U, Wevers RA. Abeling NG, et al. Among authors: van gennip ah. J Inherit Metab Dis. 1995;18(2):182-4. doi: 10.1007/BF00711761. J Inherit Metab Dis. 1995. PMID: 7564241 No abstract available.

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