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Alice Veauville

Showing results (1-10 of 7) with videos related to

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Annals of Clinical and Translational Neurology|February 6, 2020
A juvenile ALS-like phenotype dramatically improved after high-dose riboflavin treatmentChristophe Carreau, Timothée Lenglet, Isabelle Mosnier, et al.
Annales De Biologie Clinique|October 7, 2020
[Recommendations for aminoacids chromatography analysis]Alice Veauville, Cécile Acquaviva-Bourdain, Marie Nowoczyn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 22, 2020
Late-onset riboflavin transporter deficiency: a treatable mimic of various motor neuropathy aetiologiesChristophe Carreau, Charline Benoit, Guido Ahle, et al.
BMC Medical Genomics|January 31, 2020
A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA geneRobin Chautard, Cécile Laroche-Raynaud, Anne-Sophie Lia, et al.
JIMD Reports|September 28, 2015
Hyperprolinemia in Type 2 Glutaric Aciduria and MADD-Like ProfilesClément Pontoizeau, Florence Habarou, Anaïs Brassier, et al.
The New England Journal of Medicine|March 3, 2016
SLC25A32 Mutations and Riboflavin-Responsive Exercise IntoleranceManuel Schiff, Alice Veauville-Merllié, Chen Hsien Su, et al.
American Journal of Human Genetics|June 4, 2016
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Annals of Clinical and Translational Neurology|February 6, 2020
A juvenile ALS-like phenotype dramatically improved after high-dose riboflavin treatmentChristophe Carreau, Timothée Lenglet, Isabelle Mosnier, et al.
Annales De Biologie Clinique|October 7, 2020
[Recommendations for aminoacids chromatography analysis]Alice Veauville, Cécile Acquaviva-Bourdain, Marie Nowoczyn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 22, 2020
Late-onset riboflavin transporter deficiency: a treatable mimic of various motor neuropathy aetiologiesChristophe Carreau, Charline Benoit, Guido Ahle, et al.
BMC Medical Genomics|January 31, 2020
A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA geneRobin Chautard, Cécile Laroche-Raynaud, Anne-Sophie Lia, et al.
JIMD Reports|September 28, 2015
Hyperprolinemia in Type 2 Glutaric Aciduria and MADD-Like ProfilesClément Pontoizeau, Florence Habarou, Anaïs Brassier, et al.
The New England Journal of Medicine|March 3, 2016
SLC25A32 Mutations and Riboflavin-Responsive Exercise IntoleranceManuel Schiff, Alice Veauville-Merllié, Chen Hsien Su, et al.
American Journal of Human Genetics|June 4, 2016
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.
Pageof 1