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Nephrologie & Therapeutique|March 22, 2007
[Enzyme replacement therapy of Fabry's disease: the French experience]Nathalie Guffon
Presse Medicale (Paris, France : 1983)|June 5, 2007
[Overview of enzyme replacement therapy in mucopolysaccharidosis]Alain Fouilhoux, Nathalie Guffon
JIMD Reports|September 10, 2019
A rare late progression form of Sly syndrome mucopolysaccharidosisNathalie Guffon, Roseline Froissart, Alain Fouilhoux
Journal of Inherited Metabolic Disease|August 2, 2023
Fifty years of research on mitochondrial fatty acid oxidation disorders: The remaining challengesChristine Vianey-Saban, Nathalie Guffon, Alain Fouilhoux, et al.
The Journal of Pediatrics|January 27, 2009
Bone marrow transplantation in children with Hunter syndrome: outcome after 7 to 17 yearsNathalie Guffon, Yves Bertrand, Isabelle Forest, et al.
Archives of Disease in Childhood|September 4, 2012
Developing a new formulation of sodium phenylbutyrateNathalie Guffon, Yves Kibleur, William Copalu, et al.
European Journal of Pediatrics|February 12, 2019
Growth impairment and limited range of joint motion in children should raise suspicion of an attenuated form of mucopolysaccharidosis: expert opinionNathalie Guffon, Pierre Journeau, Anaïs Brassier, et al.
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