UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls von te Morsche, R H M, Drenth, J P H, Truninger, K, Schulz, H-U, Kage, A, Landt, O, Verlaan, M, Rosendahl, J, Macek, M, Jansen, J B M J, Witt, H

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Long-term olive oil-based parenteral nutrition sustains innate immune function in home patients without active underlying disease von Olthof, E.D, Roelofs, H.M.J, Versleijen, M.W.J, te Morsche, R.H.M, Simonetti, E.R, Hermans, P.W.M, Wanten, G.J.A

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Nav1.7-related small fiber neuropathy: Impaired slow-inactivation and DRG neuron hyperexcitability von HAN, C, HOEIJMAKERS, J. G. J, FABER, C. G, MERKIES, I. S. J, WAXMAN, S. G, AHN, H.-S, ZHAO, P, SHAH, P, LAURIA, G, GERRITS, M. M, TE MORSCHE, R. H. M, DIB-HAJJ, S. D, DRENTH, J. P. H

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Hepatic cyst penetration of cefazolin in patients receiving aspiration sclerotherapy von Lantinga, M A, Wijnands, T F M, Te Morsche, R H M, de Sévaux, R G L, Kuipers, S, Allegaert, K, Burger, D, Drenth, J P H

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Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia von Burns, T.M., Te Morsche, R.H.M., Jansen, J.B.M.J., H. Drenth, J.P.

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Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis von VAN ESCH, A. A. J, DE VRIES, E, TE MORSCHE, R. H. M, VAN OIJEN, M. G. H, JANSEN, J. B. M. J, DRENTH, J. P. H

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Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis von Berkhout, M., Roelofs, H. M. J., te Morsche, R. H. M., Dekker, E., van Krieken, J. H. J. M., Nagengast, F. M., Peters, W. H. M.

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Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63 von Waanders, E, Venselaar, H, Te Morsche, RHM, De Koning, DB, Kamath, PS, Torres, VE, Somlo, S, Drenth, JPH

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Prevalence of hepatitis C in the general population in the Netherlands von SLAVENBURG, S, VERDUYN-LUNEL, F. M, HERMSEN, J. T, MELCHERS, W. J. G, TE MORSCHE, R. H. M, DRENTH, J. P. H

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Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk von van der Logt, E.M.J., Bergevoet, S.M., Roelofs, H.M.J., van Hooijdonk, Z., te Morsche, R.H.M., Wobbes, T., de Kok, J.B., Nagengast, F.M., Peters, W.H.M.

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Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases von Verlaan, M, Drenth, J P H, Truninger, K, Koudova, M, Schulz, H-U, Bargetzi, M, Künzli, B, Friess, H, Cerny, M, Kage, A, Landt, O, te Morsche, R H M, Rosendahl, J, Luck, W, Nickel, R, Halangk, J, Becker, M, Macek, M, Jansen, J B M J, Witt, H

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Haptoglobin and its association with the HELLP syndrome von Raijmakers, M T M, Roes, E M, te Morsche, R H M, Steegers, E A P, Peters, W H M

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No genetic association between EPHX1 and Crohn’s disease von Peters, W H M, van der Logt, E M J, te Morsche, R H M, Roelofs, H M J, de Jong, D J, Naber, T H J

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Short mucin 6 alleles are associated with H pylori infection von Nguyen, Thai V, Janssen, Jr, Marcel, Gritters, Paulien, te Morsche, René H M, Drenth, Joost P H, van Asten, Henri, Laheij, Robert J F, Jansen, Jan B M J

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Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis von Cnossen, Wybrich R., te Morsche, René H. M., Hoischen, Alexander, Gilissen, Christian, Chrispijn, Melissa, Venselaar, Hanka, Mehdi, Soufi, Bergmann, Carsten, Veltman, Joris A., Drenth, Joost P. H.

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Novel GANAB variants associated with polycystic liver disease von van de Laarschot, Liyanne F M, Te Morsche, René H M, Hoischen, Alexander, Venselaar, Hanka, Roelofs, Hennie M, Cnossen, Wybrich R, Banales, Jesus M, Roepman, Ronald, Drenth, Joost P H

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Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis von Nickel, Renate, Sahin-Tóth, Miklós, Ózsvári, Béla, Gress, Thomas M, Truninger, Kaspar, Macek, Milan, Landt, Olfert, Büning, Carsten, Berg, Thomas, Witt, Heiko, Kovacs, Peter, Puhl, Gero, Pfützer, Roland, Groneberg, David Alexander, Kage, Andreas, Hegyi, Péter, Wiedenmann, Bertram, Bhatia, Eesh, Blüher, Matthias, Schmidt, Hartmut, te Morsche, René HM, Bödeker, Hans, Stumvoll, Michael, Teich, Niels, Schulz, Hans-Ulrich, Szmola, Richárd, Ockenga, Johann, Mössner, Joachim, Keim, Volker, Rosendahl, Jonas, Löhr, Matthias, Choudhuri, Gourdas, Drenth, Joost PH, Witt, Ulrike

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SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels von Drenth, Joost P.H., te Morsche, Rene H.M., Guillet, Gerard, Taieb, Alain, Lee Kirby, R., Jansen, Jan B.M.J.

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LRP5 variants may contribute to ADPKD von Cnossen, Wybrich R, te Morsche, René H M, Hoischen, Alexander, Gilissen, Christian, Venselaar, Hanka, Mehdi, Soufi, Bergmann, Carsten, Losekoot, Monique, Breuning, Martijn H, Peters, Dorien J M, Veltman, Joris A, Drenth, Joost P H

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Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease von Drenth, Joost P.H, te Morsche, Rene H.M, Smink, Renate, Bonifacino, Juan S, Jansen, Jan B.M.J

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