Showing results (71-80 of 121) with videos related to
Sort By:
Pageof 13
Diagnostics (Basel, Switzerland)|February 11, 2023
ECG Changes during Adult Life in Fabry Disease: Results from a Large Longitudinal Cohort StudyMohamed El Sayed, Pieter G Postema, Mareen Datema, et al.Journal of Inherited Metabolic Disease|June 19, 2021
Long-term cognitive and psychosocial outcomes in adults with phenylketonuriaLynne Aitkenhead, Gauri Krishna, Charlotte Ellerton, et al.Journal of Inherited Metabolic Disease|May 29, 2020
Subclinical effects of long-chain fatty acid β-oxidation deficiency on the adult heart: A case-control magnetic resonance studySuzan J G Knottnerus, Jeannette C Bleeker, Sacha Ferdinandusse, et al.Molecular Genetics and Metabolism|May 30, 2017
A long term follow-up study of the development of hip disease in Mucopolysaccharidosis type VIEsmee Oussoren, Johannes H J M Bessems, Virginie Pollet, et al.Clinical Journal of the American Society of Nephrology : CJASN|July 27, 2023
Early Risk Stratification for Natural Disease Course in Fabry Patients Using Plasma Globotriaosylsphingosine LevelsSanne J van der Veen, Mohamed El Sayed, Carla E M Hollak, et al.Hepatology (Baltimore, Md.)|September 5, 2009
Modulation of glycosphingolipid metabolism significantly improves hepatic insulin sensitivity and reverses hepatic steatosis in miceNora Bijl, Milka Sokolović, Carlos Vrins, et al.International Journal of Molecular Sciences|August 19, 2020
Predicting the Development of Anti-Drug Antibodies against Recombinant alpha-Galactosidase A in Male Patients with Classical Fabry DiseaseSanne J van der Veen, Wytze J Vlietstra, Laura van Dussen, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 22, 2024
Monocyte and macrophage profiles in patients with inherited long-chain fatty acid oxidation disordersSanne G S Verberk, Nico Hahn, Daan Heister, et al.JIMD Reports|November 18, 2020
Neonatal carnitine concentrations in relation to gestational age and weightLoek L Crefcoeur, Monique G M de Sain-van der Velden, Sacha Ferdinandusse, et al.Journal of Inherited Metabolic Disease|February 17, 2026
Medicine Development and Access for Rare Diseases: Can We Do Better?Carla E M Hollak, Noa Rosenberg, Colinda Post, et al.Pageof 13