Erythropoietic protoporphyria: time to prodrome, the warning signal to exit sun exposure without pain—a patient-reported outcome efficacy measure von Wensink, D., Langendonk, J. G., Overbey, J. R., Balwani, M., Van Broekhoven, E. J. E., Wagenmakers, M. A. E. M., Wilson, J. H. P., Wheeden, K., Naik, H., Desnick, R. J.

Volltext

Aceruloplasminemia presents as Type 1 diabetes in non-obese adults: a detailed case series von Vroegindeweij, L. H. P., van der Beek, E. H., Boon, A. J. W., Hoogendoorn, M., Kievit, J. A., Wilson, J. H. P., Langendonk, J. G.

Volltext

Osteoporosis in patients with erythropoietic protoporphyria von Biewenga, M., Matawlie, R.H.S., Friesema, E.C.H., Koole‐Lesuis, H., Langeveld, M., Wilson, J.H.P., Langendonk, J.G.

Volltext

Afamelanotide for Erythropoietic Protoporphyria von Langendonk, Janneke G., Balwani, Manisha, Anderson, Karl E., Bonkovsky, Herbert L., Anstey, Alexander V., Bissell, D. Montgomery, Bloomer, Joseph, Edwards, Chris, Neumann, Norbert J., Parker, Charles, Phillips, John D., Lim, Henry W., Hamzavi, Iltefat, Deybach, Jean-Charles, Kauppinen, Raili, Rhodes, Lesley E., Frank, Jorge, Murphy, Gillian M., Karstens, Francois P.J., Sijbrands, Eric J.G., de Rooij, Felix W.M., Lebwohl, Mark, Naik, Hetanshi, Goding, Colin R., Wilson, J.H. Paul, Desnick, Robert J.

Volltext

Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL von Biolcati, G., Hanneken, S., Minder, E. I., Neumann, N. J., Wilson, J. H. P., Wolgen, P. J., Wright, D. J., Lloyd, A. J.

Volltext

Aceruloplasminemia: neurodegeneration with brain iron accumulation (NBIA) associated with parkinsonism von Vroegindeweij, L. H. P., Boon, A. J. W., Wilson, J. H. P., Langendonk, J. G.

Volltext

Vitamin D deficiency in patients with erythropoietic protoporphyria von Spelt, J. M. C., de Rooij, F. W. M., Wilson, J. H. P., Zandbergen, A. A. M.

Volltext

Cardiac abnormalities in adults with the attenuated form of mucopolysaccharidosis type I von Soliman, O. I. I., Timmermans, R. G. M., Nemes, A., Vletter, W. B., Wilson, J. H. P., Cate, F. J., Geleijnse, M. L.

Volltext

Mutations of the thiopurine S-methyltransferase gene causing azathioprine intolerance in the Dutch population von Wilson, J H.P, Boor, P, de Baar-Heesakkers, E, de Rooij, F W.M

Volltext

Incidence and Mortality of Acute Pancreatitis between 1985 and 1995 von ELAND, I. A, STURKENBOOM, M. J. C. M, WILSON, J. H. P, STRICKER, B. H. Ch

Volltext

Incidence and mortality of acute pancreatitis in the Netherlands between 1985 and 1995 von Eland, I A, Sturkenboom, M J.C.M, Wilson, J H.P, Ch. Strieker, B H

Volltext

Drug-associated acute pancreatitis; 21 years of spontaneous reporting in the Netherlands von Eland, I A, van Puyenbroek, E P, Sturkenboom, M J.C.M, Wilson, J H.P, Ch. Strieker, B H

Volltext

Cancer risk in Peutz-Jeghers syndrome von Westerman, A M, Entius, M M, van Velthuysen, M L.F, Coebergh, J W.W, Lindhout, D, Offerhaus, G J.A, Wilson, J H.P

Volltext

Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome von Entius, M M, Keller, J J, Westerman, A M, van Rees, B P, van Velthuysen, M-L F, de Goeij, A F P M, Wilson, J H P, Giardiello, F M, Offerhaus, G J A

Volltext

Eicosapentaenoic acid inhibits lipolysis in weight-losing cancer patients as well as in healthy volunteers von Zuijdgeest-van Leeuwen, S D, Dagnelie, P C, Rietveld, T, Wattimena, J L.D, Swart, G R, van den Berg, J W.O, Wilson, J H.P

Volltext

Somatostatin modulates intestinal cytokine production in dextran sulfate induced colitis von van Meeteren, M E, van Bergeikj, J D, van Dijk, A P.M, Tak, C J.A.M, Wilson, J H.P, Meijssen, M A.C, Zijlstra, F J

Volltext

Biochemical basis of 5-aminolaevulinic acid-induced protoporphyrin IX accumulation: a study in patients with (pre)malignant lesions of the oesophagus von HINNEN, P, DE ROOIJ, F. W. M, VAN VELTHUYSEN, M. L. F, EDIXHOVEN, A, VAN HILLEGERSBERG, R, TILANUS, H. W, WILSON, J. H. P, SIERSEMA, P. D

Volltext

Mutation analysis in the STK11 gene in Dutch families with Peutz-Jeghers syndrome von Westerman, A M, Entius, M M, de Baar, E, Boor, P P.C, Koole-Lesuis, H, Offerhaus, G J.A, de Rooij, F W.M, Wilson, J H.P

Volltext

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome von Alhopuro, P, Katajisto, P, Lehtonen, R, Ylisaukko-oja, S K, Näätsaari, L, Karhu, A, Westerman, A M, Wilson, J H P, de Rooij, F W M, Vogel, T, Moeslein, G, Tomlinson, I P, Aaltonen, L A, Mäkelä, T P, Launonen, V

Volltext

Drug-associated anaphylaxis: 20 years of reporting in the Netherlands (1974-1994) and review of the literature von VAN DER KLAUW, M. M., WILSON, J. H. P., STRICKER, B. H. CH

Volltext