Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David Cassiman

Showing results (41-50 of 201) with videos related to

Pageof 21
Sort By:
Orphanet Journal of Rare Diseases|December 17, 2009
A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case reportDavid Cassiman, Renate Zeevaert, Elisabeth Holme, et al.
Current Protocols in Mouse Biology|June 2, 2016
An Overview of Mouse Models of Nonalcoholic Steatohepatitis: From Past to PresentAns Jacobs, Anne-Sophie Warda, Jef Verbeek, et al.
Molecular Genetics and Metabolism|September 27, 2023
Quality of life of adult patients with hereditary fructose intoleranceLise E F Janssen, David Cassiman, Martijn C G J Brouwers
The American Journal of Pathology|August 7, 2002
The vagal nerve stimulates activation of the hepatic progenitor cell compartment via muscarinic acetylcholine receptor type 3David Cassiman, Louis Libbrecht, Nicoletta Sinelli, et al.
BMC Health Services Research|October 14, 2016
Key-interventions derived from three evidence based guidelines for management and follow-up of patients with HFE haemochromatosisAnnick Vanclooster, Hub Wollersheim, Kris Vanhaecht, et al.
Clinics and Research in Hepatology and Gastroenterology|December 13, 2016
Liver failure after long-limb gastric bypassMike Ralki, David Cassiman, Jurgen Van Dongen, et al.
Orphanet Journal of Rare Diseases|October 18, 2013
Clinical evidence for orphan medicinal products-a cause for concern?Eline Picavet, David Cassiman, Carla E Hollak, et al.
Kidney Medicine|August 1, 2020
SGLT2 Inhibitors for Treatment of Refractory Hypomagnesemia: A Case Report of 3 PatientsEvan C Ray, Cary R Boyd-Shiwarski, Pengfei Liu, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 18, 2020
Fulminant Wilson Disease in Children: Recovery After Plasma Exchange Without TransplantationRenee Proost, David Cassiman, Elena Levtchenko, et al.
Gastrointestinal Endoscopy|January 22, 2018
Unusual yellow scaly colonic mucosal appearance: Tangier diseaseMathieu Struyve, Marc Ferrante, Lode van Overbeke, et al.
Pageof 21

Showing results (41-50 of 201) with videos related to

Sort By:
Pageof 21
Orphanet Journal of Rare Diseases|December 17, 2009
A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case reportDavid Cassiman, Renate Zeevaert, Elisabeth Holme, et al.
Current Protocols in Mouse Biology|June 2, 2016
An Overview of Mouse Models of Nonalcoholic Steatohepatitis: From Past to PresentAns Jacobs, Anne-Sophie Warda, Jef Verbeek, et al.
Molecular Genetics and Metabolism|September 27, 2023
Quality of life of adult patients with hereditary fructose intoleranceLise E F Janssen, David Cassiman, Martijn C G J Brouwers
The American Journal of Pathology|August 7, 2002
The vagal nerve stimulates activation of the hepatic progenitor cell compartment via muscarinic acetylcholine receptor type 3David Cassiman, Louis Libbrecht, Nicoletta Sinelli, et al.
BMC Health Services Research|October 14, 2016
Key-interventions derived from three evidence based guidelines for management and follow-up of patients with HFE haemochromatosisAnnick Vanclooster, Hub Wollersheim, Kris Vanhaecht, et al.
Clinics and Research in Hepatology and Gastroenterology|December 13, 2016
Liver failure after long-limb gastric bypassMike Ralki, David Cassiman, Jurgen Van Dongen, et al.
Orphanet Journal of Rare Diseases|October 18, 2013
Clinical evidence for orphan medicinal products-a cause for concern?Eline Picavet, David Cassiman, Carla E Hollak, et al.
Kidney Medicine|August 1, 2020
SGLT2 Inhibitors for Treatment of Refractory Hypomagnesemia: A Case Report of 3 PatientsEvan C Ray, Cary R Boyd-Shiwarski, Pengfei Liu, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 18, 2020
Fulminant Wilson Disease in Children: Recovery After Plasma Exchange Without TransplantationRenee Proost, David Cassiman, Elena Levtchenko, et al.
Gastrointestinal Endoscopy|January 22, 2018
Unusual yellow scaly colonic mucosal appearance: Tangier diseaseMathieu Struyve, Marc Ferrante, Lode van Overbeke, et al.
Pageof 21