Olivier Braissant
Inborn Errors of Metabolism
Service of Biomedicine
Lausanne University Hospital
Avenue Pierre-Decker 2
Switzerland
Name/email consistency: high
- Creatine and guanidinoacetate transport at blood-brain and blood-cerebrospinal fluid barriers. Braissant, O. J. Inherit. Metab. Dis. (2012)
- Creatine deficiency syndromes and the importance of creatine synthesis in the brain. Braissant, O., Henry, H., Béard, E., Uldry, J. Amino. Acids (2011)
- Dissociation of AGAT, GAMT and SLC6A8 in CNS: relevance to creatine deficiency syndromes. Braissant, O., Béard, E., Torrent, C., Henry, H. Neurobiol. Dis. (2010)
- Current concepts in the pathogenesis of urea cycle disorders. Braissant, O. Mol. Genet. Metab. (2010)
- Ammonia toxicity to the brain: effects on creatine metabolism and transport and protective roles of creatine. Braissant, O. Mol. Genet. Metab. (2010)
- Ammonium alters creatine transport and synthesis in a 3D culture of developing brain cells, resulting in secondary cerebral creatine deficiency. Braissant, O., Cagnon, L., Monnet-Tschudi, F., Speer, O., Wallimann, T., Honegger, P., Henry, H. Eur. J. Neurosci. (2008)
- AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: A review. Braissant, O., Henry, H. J. Inherit. Metab. Dis. (2008)
- Creatine synthesis and transport during rat embryogenesis: spatiotemporal expression of AGAT, GAMT and CT1. Braissant, O., Henry, H., Villard, A.M., Speer, O., Wallimann, T., Bachmann, C. BMC Dev. Biol. (2005)









