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Orphanet Journal of Rare Diseases
|
December 17, 2009
A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report
David 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 Present
Ans Jacobs, Anne-Sophie Warda, Jef Verbeek, et al.
Molecular Genetics and Metabolism
|
September 27, 2023
Quality of life of adult patients with hereditary fructose intolerance
Lise 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 3
David 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 haemochromatosis
Annick Vanclooster, Hub Wollersheim, Kris Vanhaecht, et al.
Clinics and Research in Hepatology and Gastroenterology
|
December 13, 2016
Liver failure after long-limb gastric bypass
Mike 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 Patients
Evan 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 Transplantation
Renee Proost, David Cassiman, Elena Levtchenko, et al.
Gastrointestinal Endoscopy
|
January 22, 2018
Unusual yellow scaly colonic mucosal appearance: Tangier disease
Mathieu Struyve, Marc Ferrante, Lode van Overbeke, et al.
Page
of 21
Search research articles
Search
Showing results (41-50 of 201) with videos related to
Sort By:
Page
of 21
Orphanet Journal of Rare Diseases
|
December 17, 2009
A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report
David 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 Present
Ans Jacobs, Anne-Sophie Warda, Jef Verbeek, et al.
Molecular Genetics and Metabolism
|
September 27, 2023
Quality of life of adult patients with hereditary fructose intolerance
Lise 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 3
David 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 haemochromatosis
Annick Vanclooster, Hub Wollersheim, Kris Vanhaecht, et al.
Clinics and Research in Hepatology and Gastroenterology
|
December 13, 2016
Liver failure after long-limb gastric bypass
Mike 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 Patients
Evan 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 Transplantation
Renee Proost, David Cassiman, Elena Levtchenko, et al.
Gastrointestinal Endoscopy
|
January 22, 2018
Unusual yellow scaly colonic mucosal appearance: Tangier disease
Mathieu Struyve, Marc Ferrante, Lode van Overbeke, et al.
Page
of 21