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Nederlands Tijdschrift Voor Geneeskunde|August 5, 2003
[From gene to disease; hepatocystin and autosomal dominant polycystic liver disease]J B M J Jansen, R H M Te Morsche, J P H Drenth
The Netherlands Journal of Medicine|June 8, 2011
Treatment extension benefits HCV genotype 1 patients without rapid virological response: a systematic reviewT J G Gevers, S Slavenburg, M G H van Oijen, et al.
Scandinavian Journal of Gastroenterology. Supplement|November 1, 2002
Genetic basis of chronic pancreatitisJ B M J Jansen, R te Morsche, H van Goor, et al.
Alimentary Pharmacology & Therapeutics|July 6, 2012
Systematic review: hypomagnesaemia induced by proton pump inhibitionM W Hess, J G J Hoenderop, R J M Bindels, et al.
The Netherlands Journal of Medicine|October 8, 2011
Hepatic and renal manifestations in autosomal dominant polycystic kidney disease: a dichotomy of two ends of a spectrumJ J M van Gulick, T J G Gevers, L van Keimpema, et al.
The British Journal of Dermatology|July 21, 2005
Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgiaT M Burns, R H M Te Morsche, J B M J Jansen, et al.
The Netherlands Journal of Medicine|December 17, 2009
Glycogenic hepatopathy: a rare cause of elevated serum transaminases in diabetes mellitusM van den Brand, L D Elving, J P H Drenth, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 17, 2020
[Safe prescribing in patients with liver cirrhosis; 5 pitfalls]R A Weersink, J P H Drenth, F Ter Borg, et al.
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