Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry
van Tuyll van Serooskerken, A.M., Drögemöller, B.I., te Velde, K., Bladergroen, R.S., Steijlen, P.M., Poblete-Gutiérrez, P., van Geel, M., van Heerden, C.J., Warnich, L., Frank, J.
Published in British journal of dermatology (1951) (01.02.2012)
Published in British journal of dermatology (1951) (01.02.2012)
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Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update
Rosipal, R., Lamoril, J., Puy, H., Da Silva, V., Gouya, L., De Rooij, F.W.M., Te Velde, K., Nordmann, Y., Martàsek, P., Deybach, J.C.
Published in Human mutation (1999)
Published in Human mutation (1999)
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Tissue-Specific Splicing Mutation in Acute Intermittent Porphyria
Grandchamp, B., Picat, C., Mignotte, V., Wilson, J. H. P., Velde, K. Te, Sandkuyl, L., Roméo, P. H., Goossens, M., Nordmann, Y.
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1989)
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1989)
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Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry: Recurrent mutation p.R59W in variegate porphyria
van Tuyll van Serooskerken, A.M., Drögemöller, B.I., te Velde, K., Bladergroen, R.S., Steijlen, P.M., Poblete-Gutiérrez, P., van Geel, M., van Heerden, C.J., Warnich, L., Frank, J.
Published in British journal of dermatology (1951) (01.02.2012)
Published in British journal of dermatology (1951) (01.02.2012)
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Detection of Latent Pernicious Anaemia
te Velde, K., Hoedemaeker, Ph. J., Anders, G. J. P. A., Arends, A., Nieweg, H. O.
Published in British Medical Journal (24.09.1966)
Published in British Medical Journal (24.09.1966)
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Jaundice in non-cirrhotic primary biliary cirrhosis: the premature ductopenic variant
Vleggaar, F P, van Buuren, H R, Zondervan, P E, ten Kate, F J W, Hop, W C J
Published in Gut (01.08.2001)
Published in Gut (01.08.2001)
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Evaluation and clinical application of the Enterotest for the determination of human biliary porphyrin composition
Beukeveld, G J, Bijleveld, C M, Kuipers, F, Kreeftenberg, H G, Huizenga, J R, te Velde, K, Wolthers, B G
Published in European journal of clinical chemistry and clinical biochemistry (01.07.1995)
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Published in European journal of clinical chemistry and clinical biochemistry (01.07.1995)
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Efficacy and safety of pravastatin in Dutch patients with hypercholesteremia and additional coronary risk factors
Huige, M.C., Bonnier, J.J.R.M., Rila, H.J., Jansen, L.J., te VElde, K., te Rijdt, A.J., de Weerd, P., Leijten, P.A.
Published in Atherosclerosis (01.06.1995)
Published in Atherosclerosis (01.06.1995)
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A family study of the initial Dutch patients with porphyria
te Velde, K, Noordhoek, K H, Wilson, J H, de Roody, F W
Published in Nederlands tijdschrift voor geneeskunde (23.12.1989)
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Published in Nederlands tijdschrift voor geneeskunde (23.12.1989)
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Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis
Gu, X F, de Rooij, F, Voortman, G, Te Velde, K, Deybach, J C, Nordmann, Y, Grandchamp, B
Published in Human genetics (01.01.1994)
Published in Human genetics (01.01.1994)
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High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria
XUE-FAN GU, DE ROOIJ, F, VOORTMAN, G, TE VELDE, K, NORDMANN, Y, GRANDCHAMP, B
Published in American journal of human genetics (01.09.1992)
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Published in American journal of human genetics (01.09.1992)
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