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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Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis von Drenth, J P H, te Morsche, R, Jansen, J B M J

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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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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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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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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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Inulin significantly improves serum magnesium levels in proton pump inhibitor‐induced hypomagnesaemia von Hess, M. W., Baaij, J. H. F., Broekman, M., Bisseling, T. M., Haarhuis, B., Tan, A., Morsche, R., Hoenderop, J. G. J., Bindels, R. J. M., 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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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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Paternal contribution to the risk for pre-eclampsia von Zusterzeel, P L M, Morsche, R te, Raijmakers, M T M, Roes, E M, Peters, W H M, Steegers, E A P

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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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Candida-specific interferon-γ deficiency and Toll-like receptor polymorphisms in patients with chronic mucocutaneous candidiasis von VAN DER GRAAF, C. A. A, NETEA, M. G, DRENTH, J. P. H, TE MORSCHE, R. H, VAN DER MEER, J. W. M, KULLBERG, B. J

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Genetic Basis of Chronic Pancreatitis von Jansen, J. B. M. J., Morsche, R. te, Goor, H. van, Drenth, J. P. H.

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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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Deletion mutation of sodium channel NaV1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitability von Cheng, Xiaoyang, Dib-Hajj, Sulayman D., Tyrrell, Lynda, te Morsche, Rene H., Drenth, Joost P. H., Waxman, Stephen G.

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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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Chronic yersiniosis due to defects in the TLR5 and NOD2 recognition pathways von NETEA, M. G, VAN DER LEIJ, F, DRENTH, J. P. H, JOOSTEN, L. A. B, TE MORSCHE, R, VERWEIJ, P, DE JONG, D, KULLBERG, B. J, VAN DER MEET, J. W. M

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