Search research articles
Contact Us
Filters
Showing results (141-150 of 201) with videos related to
Page
of 21
Sort By:
Journal of Inherited Metabolic Disease
|
June 29, 2010
Alpers syndrome presenting with anatomopathological features of fulminant autoimmune hepatitis
Peter 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 Cultures
Kim 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 Disease
Liam 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 disease
Marie 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 mechanism
Chandran 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 shock
Koen 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 transplantation
Philip 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 carcinoma
Hannah 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 intolerance
Evi 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 controls
Willem G van Ginkel, Rianne Jahja, Stephan C J Huijbregts, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 201) with videos related to
Sort By:
Page
of 21
Journal of Inherited Metabolic Disease
|
June 29, 2010
Alpers syndrome presenting with anatomopathological features of fulminant autoimmune hepatitis
Peter 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 Cultures
Kim 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 Disease
Liam 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 disease
Marie 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 mechanism
Chandran 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 shock
Koen 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 transplantation
Philip 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 carcinoma
Hannah 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 intolerance
Evi 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 controls
Willem G van Ginkel, Rianne Jahja, Stephan C J Huijbregts, et al.
Page
of 21