Long-Term Efficacy and Safety of Pegvisomant in Combination With Long-Acting Somatostatin Analogs in Acromegaly von Neggers, S. J. C. M. M, Franck, S. E, de Rooij, F. W. M, Dallenga, A. H. G, Poublon, R. M. L, Feelders, R. A, Janssen, J. A. M. J. L, Buchfelder, M, Hofland, L. J, Jørgensen, J. O. L, van der Lely, A. J

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Common variants in PCSK1 influence blood pressure and body mass index von Gu, Q, Yazdanpanah, M, van Hoek, M, Hofman, A, Gao, X, de Rooij, F W M, Sijbrands, E J G

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Porphyrin biosynthesis in human Barrett's oesophagus and adenocarcinoma after ingestion of 5-aminolaevulinic acid von HINNEN, P, DE ROOIJ, F. W. M, TERLOUW, E. M, EDIXHOVEN, A, VAN DEKKEN, H, VAN HILLEGERSBERG, R, TILANUS, H. W, WILSON, J. H. P, SIERSEMA, P. D

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HDL associates with insulin resistance and beta-cell dysfunction in South Asian families at risk of type 2 diabetes von Yahya, R., Jainandunsing, S., Rashid, M., van der Zee, L., Touw, A., de Rooij, F.W.M., Sijbrands, E.J.G., Verhoeven, A.J.M., Mulder, M.T.

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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.

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Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates von de Leng, WWJ, Jansen, M, Carvalho, R, Polak, M, Musler, AR, Milne, ANA, Keller, JJ, Menko, FH, de Rooij, FWM, Iacobuzio-Donahue, CA, Giardiello, FM, Weterman, MAJ, Offerhaus, GJA

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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

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High cancer risk and increased mortality in patients with Peutz–Jeghers syndrome von van Lier, Margot G F, Westerman, Anne Marie, Wagner, Anja, Looman, Caspar W N, Wilson, J H Paul, de Rooij, Felix W M, Lemmens, Valery E P P, Kuipers, Ernst J, Mathus-Vliegen, Elisabeth M H, van Leerdam, Monique E

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A Gly15Arg Mutation in the Interleukin-10 Gene Reduces Secretion of Interleukin-10 in Crohn Disease von VAN DER LINDE, K, BOOR, P. P. C, SANDKUIJL, L. A, MEIJSSEN, M. A. C, SAVELKOUL, H. F. J, WILSON, J. H. P, DE ROOIJ, F. W. M

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STRAD in Peutz-Jeghers syndrome and sporadic cancers von de Leng, W W J, Keller, J J, Luiten, S, Musler, A R, Jansen, M, Baas, A F, de Rooij, F W M, Gille, J J P, Menko, F H, Offerhaus, G J A, Weterman, M A J

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LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome von Volikos, E, Robinson, J, Aittomäki, K, Mecklin, J-P, Järvinen, H, Westerman, A M, de Rooji, F W M, Vogel, T, Moeslein, G, Launonen, V, Tomlinson, I P M, Silver, A R J, Aaltonen, L A

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Acrylate yellow filters in operating lights protect against photosensitization tissue damage von Hinnen, P., de Rooij, F. W. M., Voortman, G., Tilanus, H. W., Wilson, J. H. P., Siersema, P. D.

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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

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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

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Peutz-Jeghers syndrome: 78-year follow-up of the original family von Westerman, Anne Marie, Entius, Mark M, de Baar, Ellen, Boor, Patrick PC, Koole, Rita, van Velthuysen, M Loes F, Offerhaus, G Johan A, Lindhout, Dick, de Rooij, Felix WM, Wilson, JH Paul

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A functional interleukin-10 mutation in Dutch patients with Crohn's disease von van der Linde, K., Boor, P.P.C., van Bodegraven, A.A., de Jong, D.J., Crusius, J.B.A., Naber, T.H.J., Kuipers, E.J., Wilson, J.H.P., de Rooij, F.W.M.

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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, 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

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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRAD , and MO25 , 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, F W M de Rooij, Vogel, T, Moeslein, G, Tomlinson, I P, Aaltonen, L A, Mäkelä, T P, Launonen, V

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Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria von Picat, C., Delfau, M. H., Rooij, F. W. M., Beukeveld, G. J. J., Wolthers, B. G., Wadman, S. K., Nordmann, Y., Grandchamp, B.

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Kinetics, localization, and mechanism of 5-aminolevulinic acid-induced porphyrin accumulation in normal and Barrett's-like rat esophagus von van den Boogert, Jolanda, Houtsmuller, Adriaan B., de Rooij, Felix W.M., de Bruin, Ron W.F., Siersema, Peter D., van Hillegersberg, Richard

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