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La Revue De Medecine Interne|April 29, 2006
[Current and future biochemical markers for Gaucher disease]R FroissartArchives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2014
[Laboratory diagnosis and follow up of mucopolysaccharidoses]R Froissart, S BekriLa Revue De Medecine Interne|January 8, 2011
[Contribution of genotyping in Fabry's disease]R Froissart, M Piraud, I MaireLa Revue De Medecine Interne|January 8, 2011
[Contribution of the measurement of globotriaosylceramide in urine to the diagnosis and follow-up of Fabry disease]M Piraud, I Maire, R FroissartLa Revue De Medecine Interne|January 30, 2008
[Current development and usefulness of biomarkers for Gaucher disease follow up]I Maire, N Guffon, R FroissartThe Biochemical Journal|August 15, 1997
Characterization of iduronate sulphatase mutants affecting N-glycosylation sites and the cysteine-84 residueG Millat, R Froissart, I Maire, et al.Experimental Cell Research|February 1, 1997
IDS transfer from overexpressing cells to IDS-deficient cellsG Millat, R Froissart, I Maire, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|May 19, 2010
The virulence-transmission trade-off in vector-borne plant viruses: a review of (non-)existing studiesR Froissart, J Doumayrou, F Vuillaume, et al.Biochimica Et Biophysica Acta|September 29, 1999
The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signalsS Cudry, R Froissart, O Bouton, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|April 30, 1996
Amniotic fluid for screening of lysosomal storage diseases presenting in utero (mainly as non-immune hydrops fetalis)M Piraud, R Froissart, G Mandon, et al.Pageof 5