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Revue Medicale Suisse|February 23, 2023
[Inborn errors of metabolism: a specialty at the forefront of precision medicine]Ilse Kern, Piotr Foland, Diana BallhausenMolecular Genetics and Metabolism|September 28, 2011
The unsolved puzzle of neuropathogenesis in glutaric aciduria type IParis Jafari, Olivier Braissant, Luisa Bonafé, et al.Pediatric Reports|February 23, 2012
Born at 27 weeks of gestation with classical PKU: challenges of dietetic management in a very preterm infantDiana Ballhausen, Delphine Egli, Myriam Bickle-Graz, et al.Revue Medicale Suisse|March 22, 2012
[New therapies for children affected by bone diseases]Diana Ballhausen, Nuria Garcia Dépraz, Ilse Kern, et al.Plos One|January 18, 2013
Ammonium accumulation and cell death in a rat 3D brain cell model of glutaric aciduria type IParis Jafari, Olivier Braissant, Petra Zavadakova, et al.Journal of Neurochemistry|October 3, 2002
Hydroxylated residues influence desensitization behaviour of recombinant alpha3 glycine receptor channelsHans-Georg Breitinger, Carmen Villmann, Janine Rennert, et al.Orphanet Journal of Rare Diseases|January 10, 2013
Brain damage in methylmalonic aciduria: 2-methylcitrate induces cerebral ammonium accumulation and apoptosis in 3D organotypic brain cell culturesParis Jafari, Olivier Braissant, Petra Zavadakova, et al.Molecular Genetics and Metabolism Reports|September 10, 2021
The impact of disease severity on the psychological well-being of youth affected by an inborn error of metabolism and their families: A one-year longitudinal studyNevena Dimitrova, Jennifer Glaus, Sébastien Urben, et al.Epilepsia|May 16, 2008
Glut-1 deficiency syndrome masquerading as idiopathic generalized epilepsyEliane Roulet-Perez, Diana Ballhausen, Luisa Bonafé, et al.Cells|July 11, 2025
Structural and Functional Characterization of N-Glycanase-1 Pathogenic VariantsAntje Banning, Lukas Hoeren, Isis Atallah, et al.Pageof 6