de Rooij FW - Search Results

1

Residual activity of human porphobilinogen deaminase with R167Q or R167W mutations: an explanation for survival of homozygous and compound heterozygous acute intermittent porphyrics.

Edixhoven-Bosdijk A, de Rooij FW, de Baar-Heesakkers E, Wilson JH. Edixhoven-Bosdijk A, et al. Among authors: de baar heesakkers e, de rooij fw. Cell Mol Biol (Noisy-le-grand). 2002 Dec;48(8):861-6. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 12699244

2

Two course illuminating scheme improves aminolevulinic acid photodynamic therapy in cell cultures.

Hinnen P, Siersema PD, Edixhoven A, Wilson JH, de Rooij FW. Hinnen P, et al. Among authors: de rooij fw. Cell Mol Biol (Noisy-le-grand). 2002 Dec;48(8):903-9. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 12699249

3

Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands.

de Rooij FW, Kavelaars FG, Koole-Lesuis H, Wilson JH. de Rooij FW, et al. Cell Mol Biol (Noisy-le-grand). 2009 Jul 1;55(2):64-9. Cell Mol Biol (Noisy-le-grand). 2009. PMID: 19656453

4

Erythrocyte porphobilinogen deaminase activity in porphyria cutanea tarda.

Siersema PD, de Rooij FW, Edixhoven-Bosdijk A, Wilson JH. Siersema PD, et al. Among authors: de rooij fw. Clin Chem. 1990 Oct;36(10):1779-83. Clin Chem. 1990. PMID: 2208654

5

The activity of erythrocyte porphobilinogen deaminase in familial and sporadic forms of porphyria cutanea tarda.

Siersema PD, de Rooij FW, Edixhoven-Bosdijk A, Wilson JH. Siersema PD, et al. Among authors: de rooij fw. Curr Probl Dermatol. 1991;20:116-22. doi: 10.1159/000420015. Curr Probl Dermatol. 1991. PMID: 1935203 No abstract available.

6

Heme synthesis in chronic renal failure: the effects of hemodialysis, peritoneal dialysis and erythropoietin treatment.

Siersema PD, de Rooij FW, Edixhoven-Bosdijk A, Weimar W, Wilson JH. Siersema PD, et al. Among authors: de rooij fw. Nephron. 1995;71(3):297-302. doi: 10.1159/000188735. Nephron. 1995. PMID: 8569978

7

[From gene to disease; 'frame shift'-mutation in the CARD15-gene and Crohn's disease].

van der Linde K, Kuipers EJ, de Rooij FW, Wilson JH. van der Linde K, et al. Among authors: de rooij fw. Ned Tijdschr Geneeskd. 2002 Dec 28;146(52):2539-42. Ned Tijdschr Geneeskd. 2002. PMID: 12532667 Dutch.

8

Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria.

Delfau MH, Picat C, de Rooij FW, Hamer K, Bogard M, Wilson JH, Deybach JC, Nordmann Y, Grandchamp B. Delfau MH, et al. Among authors: de rooij fw. J Clin Invest. 1990 Nov;86(5):1511-6. doi: 10.1172/JCI114869. J Clin Invest. 1990. PMID: 2243128 Free PMC article.

9

Vitamin D deficiency in patients with erythropoietic protoporphyria.

Spelt JM, de Rooij FW, Wilson JH, Zandbergen AA. Spelt JM, et al. Among authors: de rooij fw. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S1-4. doi: 10.1007/s10545-008-1037-0. J Inherit Metab Dis. 2010. PMID: 24137761

10

Purification of porphobilinogen deaminase from human erythrocytes by fast protein liquid chromatography.

de Rooij FW, Hamer CM, Wilson JH. de Rooij FW, et al. Clin Chim Acta. 1987 Jan 15;162(1):61-8. doi: 10.1016/0009-8981(87)90233-6. Clin Chim Acta. 1987. PMID: 3802547

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