van Diggelen OP - Search Results

1

First trimester diagnosis of Hunter syndrome on chorionic villi.

Kleijer WJ, van Diggelen OP, Janse HC, Galjaard H, Dumez Y, Boué J. Kleijer WJ, et al. Among authors: van diggelen op. Lancet. 1984 Aug 25;2(8400):472. doi: 10.1016/s0140-6736(84)92952-0. Lancet. 1984. PMID: 6147543 No abstract available.

2

First-trimester diagnosis of galactosaemia.

Kleijer WJ, Janse HC, van Diggelen OP, Macek M, Hajek Z, Gillett MG, Holton JB. Kleijer WJ, et al. Among authors: van diggelen op. Lancet. 1986 Mar 29;1(8483):748. doi: 10.1016/s0140-6736(86)91149-9. Lancet. 1986. PMID: 2870264 No abstract available.

3

First trimester diagnosis of Wolman's disease.

van Diggelen OP, von Koskull H, Ammälä P, Vredeveldt GT, Janse HC, Kleijer WJ. van Diggelen OP, et al. Prenat Diagn. 1988 Nov;8(9):661-3. doi: 10.1002/pd.1970080905. Prenat Diagn. 1988. PMID: 3211854

4

Disaccharidases in amniotic fluid as possible prenatal marker for cystic fibrosis.

van Diggelen OP, Janse HC, Kleijer WJ. van Diggelen OP, et al. Lancet. 1983 Apr 9;1(8328):817. doi: 10.1016/s0140-6736(83)91869-x. Lancet. 1983. PMID: 6132147 No abstract available.

5

Debranching enzyme in fibroblasts, amniotic fluid cells and chorionic villi: pre- and postnatal diagnosis of glycogenosis type III.

van Diggelen OP, Janse HC, Smit GP. van Diggelen OP, et al. Clin Chim Acta. 1985 Jul 15;149(2-3):129-34. doi: 10.1016/0009-8981(85)90326-2. Clin Chim Acta. 1985. PMID: 3161667

6

Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease.

van Diggelen OP, Schindler D, Kleijer WJ, Huijmans JM, Galjaard H, Linden HU, Peter-Katalinic J, Egge H, Dabrowski U, Cantz M. van Diggelen OP, et al. Lancet. 1987 Oct 3;2(8562):804. doi: 10.1016/s0140-6736(87)92542-6. Lancet. 1987. PMID: 2889023 No abstract available.

7

First-trimester diagnosis of Morquio disease type A.

Kleijer WJ, Geilen GC, Garritsen V, Huijmans JG, Los FJ, Voznyi YV, van Diggelen OP. Kleijer WJ, et al. Among authors: van diggelen op. Prenat Diagn. 2000 Mar;20(3):183-5. Prenat Diagn. 2000. PMID: 10719317

8

Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay.

Keulemans JL, Sinigerska I, Garritsen VH, Huijmans JG, Voznyi YV, van Diggelen OP, Kleijer WJ. Keulemans JL, et al. Among authors: van diggelen op. Prenat Diagn. 2002 Nov;22(11):1016-21. doi: 10.1002/pd.457. Prenat Diagn. 2002. PMID: 12424767

9

Enzymatic diagnosis of Morquio A syndrome with a new fluorimetric substrate.

Zhao H, van Diggelen OP, Kleijer WJ, Li P. Zhao H, et al. Among authors: van diggelen op. Chin Med Sci J. 1991 Mar;6(1):9-13. Chin Med Sci J. 1991. PMID: 1786409

10

A fluorimetric enzyme assay for the diagnosis of Morquio disease type A (MPS IV A).

van Diggelen OP, Zhao H, Kleijer WJ, Janse HC, Poorthuis BJ, van Pelt J, Kamerling JP, Galjaard H. van Diggelen OP, et al. Among authors: van pelt j. Clin Chim Acta. 1990 Feb 28;187(2):131-9. doi: 10.1016/0009-8981(90)90339-t. Clin Chim Acta. 1990. PMID: 2107987

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