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F Lammert

Showing results (91-100 of 117) with videos related to

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Journal of Hepatology|October 30, 2001
Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: soluble pronucleating proteins in gallbladder and hepatic bilesK J van Erpecum, D Q Wang, F Lammert, et al.
Endoscopy|April 3, 2009
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screeningR Hüneburg, F Lammert, C Rabe, et al.
Alimentary Pharmacology & Therapeutics|December 9, 2010
Heterozygosity for the alpha1-antitrypsin Z allele may confer genetic risk of cholangiocarcinomaF Mihalache, A Höblinger, F Grünhage, et al.
Neurogastroenterology and Motility|April 17, 2009
Absence of the interstitial cell of Cajal network in mitochondrial neurogastrointestinal encephalomyopathyV Zimmer, W Feiden, G Becker, et al.
Digestion|January 30, 2010
Genotypic interaction and gender specificity of common genetic variants in the p53/mdm2 network in Crohn's diseaseV Zimmer, T Widmann, M Müller, et al.
Journal of Gastroenterology and Hepatology|August 18, 2025
Hepatic Inflammation and Liver Injury in a Model of Bacterial Infection Triggered Acute-on-Chronic Liver InjuryS C Karatayli, S N Weber, R A Hall, et al.
Die Ophthalmologie|August 4, 2022
[Economics of operating room use at a university eye hospital]C Framme, T Kuiper, W Lobbes, et al.
European Journal of Medical Research|June 18, 2010
Transient elastography discloses identical distribution of liver fibrosis in chronic hepatitis C between HIV-negative and HIV-positive patients on HAARTF Grünhage, J-C Wasmuth, S Herkenrath, et al.
Clinical Genetics|April 6, 2013
Novel ceruloplasmin mutation causing aceruloplasminemia with hepatic iron overload and diabetes without neurological symptomsM Rusticeanu, V Zimmer, L Schleithoff, et al.
Gut|August 8, 2006
Intrahepatic cholestasis of pregnancy: the severe form is associated with common variants of the hepatobiliary phospholipid transporter ABCB4 geneH E Wasmuth, A Glantz, H Keppeler, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Journal of Hepatology|October 30, 2001
Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: soluble pronucleating proteins in gallbladder and hepatic bilesK J van Erpecum, D Q Wang, F Lammert, et al.
Endoscopy|April 3, 2009
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screeningR Hüneburg, F Lammert, C Rabe, et al.
Alimentary Pharmacology & Therapeutics|December 9, 2010
Heterozygosity for the alpha1-antitrypsin Z allele may confer genetic risk of cholangiocarcinomaF Mihalache, A Höblinger, F Grünhage, et al.
Neurogastroenterology and Motility|April 17, 2009
Absence of the interstitial cell of Cajal network in mitochondrial neurogastrointestinal encephalomyopathyV Zimmer, W Feiden, G Becker, et al.
Digestion|January 30, 2010
Genotypic interaction and gender specificity of common genetic variants in the p53/mdm2 network in Crohn's diseaseV Zimmer, T Widmann, M Müller, et al.
Journal of Gastroenterology and Hepatology|August 18, 2025
Hepatic Inflammation and Liver Injury in a Model of Bacterial Infection Triggered Acute-on-Chronic Liver InjuryS C Karatayli, S N Weber, R A Hall, et al.
Die Ophthalmologie|August 4, 2022
[Economics of operating room use at a university eye hospital]C Framme, T Kuiper, W Lobbes, et al.
European Journal of Medical Research|June 18, 2010
Transient elastography discloses identical distribution of liver fibrosis in chronic hepatitis C between HIV-negative and HIV-positive patients on HAARTF Grünhage, J-C Wasmuth, S Herkenrath, et al.
Clinical Genetics|April 6, 2013
Novel ceruloplasmin mutation causing aceruloplasminemia with hepatic iron overload and diabetes without neurological symptomsM Rusticeanu, V Zimmer, L Schleithoff, et al.
Gut|August 8, 2006
Intrahepatic cholestasis of pregnancy: the severe form is associated with common variants of the hepatobiliary phospholipid transporter ABCB4 geneH E Wasmuth, A Glantz, H Keppeler, et al.
Pageof 12