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David Cassiman

Showing results (141-150 of 201) with videos related to

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Journal of Inherited Metabolic Disease|June 29, 2010
Alpers syndrome presenting with anatomopathological features of fulminant autoimmune hepatitisPeter Witters, Jacques Pirenne, Raymond Aerts, et al.
Plos One|August 7, 2015
Synergistic Activity of the Plant Defensin HsAFP1 and Caspofungin against Candida albicans Biofilms and Planktonic CulturesKim Vriens, Tanne L Cools, Peta J Harvey, et al.
JIMD Reports|October 14, 2014
Clinical, Biochemical, and Molecular Characterization of Novel Mutations in ABCA1 in Families with Tangier DiseaseLiam R Brunham, Martin H Kang, Clara Van Karnebeek, et al.
Orphanet Journal of Rare Diseases|May 13, 2026
Screening for acid sphingomyelinase deficiency in patients with an interstitial lung diseaseMarie Vermant, Ilse Van Raemdonck, Nathalie Veyt, et al.
Haematologica|July 14, 2018
The <i>SLC40A1</i> R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanismChandran Ka, Julie Guellec, Xavier Pepermans, et al.
The Journal of Pediatrics|February 18, 2011
Left ventricular assist device as bridge to liver transplantation in a patient with propionic acidemia and cardiogenic shockKoen Ameloot, Dirk Vlasselaers, Matthias Dupont, et al.
European Journal of Gastroenterology & Hepatology|May 11, 2013
Heterozygous α1-antitrypsin Z allele mutation in presumed healthy donor livers used for transplantationPhilip Roelandt, Pieter Dobbels, Mina Komuta, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|May 3, 2012
Histology obtained by needle biopsy gives additional information on the prognosis of hepatocellular carcinomaHannah van Malenstein, Mina Komuta, Chris Verslype, et al.
The Journal of Clinical Investigation|February 11, 2025
Safety and efficacy of pharmacological inhibition of ketohexokinase in hereditary fructose intoleranceEvi Jc Koene, Amée M Buziau, David Cassiman, et al.
Orphanet Journal of Rare Diseases|July 1, 2016
Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controlsWillem G van Ginkel, Rianne Jahja, Stephan C J Huijbregts, et al.
Pageof 21

Showing results (141-150 of 201) with videos related to

Sort By:
Pageof 21
Journal of Inherited Metabolic Disease|June 29, 2010
Alpers syndrome presenting with anatomopathological features of fulminant autoimmune hepatitisPeter Witters, Jacques Pirenne, Raymond Aerts, et al.
Plos One|August 7, 2015
Synergistic Activity of the Plant Defensin HsAFP1 and Caspofungin against Candida albicans Biofilms and Planktonic CulturesKim Vriens, Tanne L Cools, Peta J Harvey, et al.
JIMD Reports|October 14, 2014
Clinical, Biochemical, and Molecular Characterization of Novel Mutations in ABCA1 in Families with Tangier DiseaseLiam R Brunham, Martin H Kang, Clara Van Karnebeek, et al.
Orphanet Journal of Rare Diseases|May 13, 2026
Screening for acid sphingomyelinase deficiency in patients with an interstitial lung diseaseMarie Vermant, Ilse Van Raemdonck, Nathalie Veyt, et al.
Haematologica|July 14, 2018
The <i>SLC40A1</i> R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanismChandran Ka, Julie Guellec, Xavier Pepermans, et al.
The Journal of Pediatrics|February 18, 2011
Left ventricular assist device as bridge to liver transplantation in a patient with propionic acidemia and cardiogenic shockKoen Ameloot, Dirk Vlasselaers, Matthias Dupont, et al.
European Journal of Gastroenterology & Hepatology|May 11, 2013
Heterozygous α1-antitrypsin Z allele mutation in presumed healthy donor livers used for transplantationPhilip Roelandt, Pieter Dobbels, Mina Komuta, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|May 3, 2012
Histology obtained by needle biopsy gives additional information on the prognosis of hepatocellular carcinomaHannah van Malenstein, Mina Komuta, Chris Verslype, et al.
The Journal of Clinical Investigation|February 11, 2025
Safety and efficacy of pharmacological inhibition of ketohexokinase in hereditary fructose intoleranceEvi Jc Koene, Amée M Buziau, David Cassiman, et al.
Orphanet Journal of Rare Diseases|July 1, 2016
Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controlsWillem G van Ginkel, Rianne Jahja, Stephan C J Huijbregts, et al.
Pageof 21