ACNP - Italian Periodicals Catalogue

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Results: 10

A gastric diverticulum containing pancreatic tissue and presenting as congenital double pylorus: Case report and review of the literature

Authors: Wolters, VM Nikkels, PGJ Van Der Zee, DC Kramer, PPG De Schryver, JEAR Reijnen, IGM Houwen, RHJ

Citation: Vm. Wolters et al., A gastric diverticulum containing pancreatic tissue and presenting as congenital double pylorus: Case report and review of the literature, J PED GASTR, 33(1), 2001, pp. 89-91

FIC1 disease: A spectrum of intrahepatic cholestatic disorders

Authors: van Mil, SWC Klomp, LWJ Bull, LN Houwen, RHJ

Citation: Swc. Van Mil et al., FIC1 disease: A spectrum of intrahepatic cholestatic disorders, SEM LIV DIS, 21(4), 2001, pp. 535-544

FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte

Authors: Eppens, EF van Mil, SWC de Vree, JM Mok, KS Juijn, JA Elferink, RPJO Berger, R Houwen, RHJ Klomp, LWJ

Citation: Ef. Eppens et al., FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte, J HEPATOL, 35(4), 2001, pp. 436-443

A missense mutation in FIC1 is associated with Greenland familial cholestasis

Authors: Klomp, LWJ Bull, LN Knisely, AS van der Doelen, MAM Juijn, JA Berger, R Forget, S Nielsen, IM Eiberg, H Houwen, RHJ

Citation: Lwj. Klomp et al., A missense mutation in FIC1 is associated with Greenland familial cholestasis, HEPATOLOGY, 32(6), 2000, pp. 1337-1341

Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes

Authors: Muller, T Wijmenga, C Phillips, AD Janecke, A Houwen, RHJ Fischer, H Ellemunter, H Fruhwirth, M Offner, F Hofer, S Muller, W Booth, IW Heinz-Erian, P

Citation: T. Muller et al., Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes, GASTROENTY, 119(6), 2000, pp. 1506-1513

Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC (vol 104, pg 241, 1999)

Authors: Bull, LN Juijn, JA Liao, M van Eijk, MJT Sinke, RJ Stricker, NL DeYoung, JA Carlton, VEH Baharloo, S Klomp, LWJ Abukawa, D Barton, DE Bass, NM Bourke, B Drumm, B Jankowska, I Lovisetto, P McQuaid, S Pawlowska, J Tazawa, Y Villa, E Tygstrup, N Berger, R Knisely, AS Houwen, RHJ Freimer, NB

Citation: Ln. Bull et al., Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC (vol 104, pg 241, 1999), HUM GENET, 104(6), 1999, pp. 528-528

Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC

Citation: Ln. Bull et al., Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC, HUM GENET, 104(3), 1999, pp. 241-248

Skinfold measurements in children with cystic fibrosis: monitoring fat-free mass and exercise effects

Authors: de Meer, K Gulmans, VAM Westerterp, KR Houwen, RHJ Berger, R

Citation: K. De Meer et al., Skinfold measurements in children with cystic fibrosis: monitoring fat-free mass and exercise effects, EUR J PED, 158(10), 1999, pp. 800-806

Recurrent familial intrahepatic cholestasis in the Faeroe Islands. Phenotypic heterogeneity but genetic homogeneity

Authors: Tygstrup, N Steig, BA Juijn, JA Bull, LN Houwen, RHJ

Citation: N. Tygstrup et al., Recurrent familial intrahepatic cholestasis in the Faeroe Islands. Phenotypic heterogeneity but genetic homogeneity, HEPATOLOGY, 29(2), 1999, pp. 506-508

Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson'sdisease

Authors: Wijmenga, C Muller, T Murli, IS Brunt, T Feichtinger, H Schonitzer, D Houwen, RHJ Muller, W Sandkuijl, LA Pearson, PL

Citation: C. Wijmenga et al., Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson'sdisease, EUR J HUM G, 6(6), 1998, pp. 624-628

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