Medical and financial burden of acute intermittent porphyria von Neeleman, Rochus A., Wagenmakers, Margreet A. E. M., Koole-Lesuis, Rita H., Mijnhout, G. Sophie, Wilson, J. H. Paul, Friesema, Edith C. H., Langendonk, Janneke G.

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Transcription factor 7-like 2 gene links increased in vivo insulin synthesis to type 2 diabetes von Jainandunsing, Sjaam, Koole, H. Rita, van Miert, Joram N.I., Rietveld, Trinet, Wattimena, J.L. Darcos, Sijbrands, Eric J.G., de Rooij, Felix W.M.

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Correction to: Medical and financial burden of acute intermittent porphyria von Neeleman, Rochus A., Wagenmakers, Margreet A. E. M., Koole-Lesuis, Rita H., Mijnhout, G. Sophie, Wilson, J. H. Paul, Friesema, Edith C. H., Langendonk, Janneke G.

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Digenic Inheritance of Mutations in the Coproporphyrinogen Oxidase and Protoporphyrinogen Oxidase Genes in a Unique Type of Porphyria von van Tuyll van Serooskerken, Anne Moniek, de Rooij, Felix W., Edixhoven, Annie, Bladergroen, Reno S., Baron, Jens M., Joussen, Sylvia, Merk, Hans F., Steijlen, Peter M., Poblete-Gutiérrez, Pamela, te Velde, Kornelis, Paul Wilson, J.H., Koole, Rita H., van Geel, Michel, Frank, Jorge

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Novel null-allele mutations and genotype-phenotype correlation in Argentinean patients with erythropoietic protoporphyria von Parera, Victoria E, Koole, Rita H, Minderman, Gardi, Edixhoven, Annie, Rossetti, Maria V, Batlle, Alcira, de Rooij, Felix W M

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Abstract 339: Splice Acceptor Site Mutation in Cullin 3 is Causing Pseudohypoaldosteronism Type II von Friesema, Edith C, Verkerk, Annemieke J, Koole, Rita H, van der Lubbe, Nils, van Rooij, Jeroen, Kraaij, Robert, Uitterlinden, Andre G, Sijbrands, Eric J, van den Meiracker, Anton H

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Clinical Remission of Delta‐Aminolevulinic Acid Dehydratase Deficiency Through Suppression of Erythroid Heme Synthesis von Neeleman, Rochus A., van Beers, Eduard J., Friesema, Edith C., Koole‐Lesuis, Rita, van der Pol, Willem L., Wilson, J.H. Paul, Langendonk, Janneke G.

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Effect of HIPEC according to HRD / BRCA wt genomic profile in stage III ovarian cancer: Results from the phase III OVHIPEC trial von Koole, Simone N., Schouten, Philip C., Hauke, Jan, Kluin, Roel J. C., Nederlof, Petra, Richters, Lisa K., Krebsbach, Gabriele, Sikorska, Karolina, Alkemade, Maartje, Opdam, Mark, Schagen van Leeuwen, Jules H., Schreuder, Henk W. R., Hermans, Ralph H. M., de Hingh, Ignace H. J. T., Mom, Constantijne H., Arts, Henriette J. G., van Ham, Maaike, van Dam, Peter, Vuylsteke, Peter, Sanders, Joyce, Horlings, Hugo M., van de Vijver, Koen K., Hahnen, Eric, van Driel, Willemien J., Schmutzler, Rita, Sonke, Gabe S., Linn, Sabine C.

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Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency through Suppression of Erythroid Heme Synthesis von Neeleman, Rochus A, van Beers, Eduard J, Friesema, Edith C, Koole-Lesuis, Rita, van der Pol, Willem L, Wilson, J H Paul, Langendonk, Janneke G

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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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Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families von Westerman, Anne Marie, Entius, Mark M., Boor, Patrick P.C., Koole, Rita, Baar, Ellen de, Offerhaus, G. Johan A., Lubinski, Jan, Lindhout, Dick, Halley, Dicky J.J., de Rooij, Felix W.M., Wilson, J.H. Paul

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Faecal haem assay — some practical modifications of the haemoquant assay for haemoglobin in faeces von van den Berg, J.Willem O., Edixhoven-Bosdijk, Annie, Koole-Lesuis, Rita, Wilson, J.H.Paul

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