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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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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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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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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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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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, FWW, van Velthuysen, MLF, Edixhoven, A, van Hillegersberg, R, Tilanus, HW, Wilson, JHP, Siersema, PD

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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

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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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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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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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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

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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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Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update von 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.

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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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Two different point G to a mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria von DELFAU, M. H, PICAT, C, DE ROOIJ, F. W. M, HAMER, K, BOGARD, M, WILSON, J. H. P, DEYBACH, J. C, NORDMANN, Y, GRANDCHAMP, B

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Pharmacokinetics of 5-aminolevulinic acid-induced protoporphyrin-IX in tissues and plasma of patients with Barrettʼs esophagus von Hinnen, P., de Rooij, F. W.M., Hop, W. C.J., Edixhoven, A., Wilson, J. H.P., Siersema, P. D.

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Primary Bile Acid Malabsorption: A Pathophysiologic and Clinical Entity? von Van Tilburg, A. J. P., De Rooij, F. W. M., Van Den Berg, J. W. O., Van Blankenstein, M.

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Na+-dependent bile acid transport in the ileum: The balance between diarrhea and constipation von Van Tilburg, A.J.P., De Rooij, F.W.M., Van Blankenstein, M., Van Den Berg, J.W.O., Bosman-Jacobs, E.P.

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The selenium-75-homocholic acid taurine test reevaluated: combined measurement of fecal selenium-75 activity and 3 alpha-hydroxy bile acids in 211 patients von van Tilburg, A J, de Rooij, F W, van den Berg, J W, Kooij, P P, van Blankenstein, M

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