Carglumic acid: an additional therapy in the treatment of organic acidurias with hyperammonemia?
2008 · Orphanet Journal of Rare Diseases · 40 citations
https://doi.org/10.1186/1750-1172-3-2
A
Alain Fouilhoux
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48
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16
h-index
19
i10-index
Alain Fouilhoux is an academic researcher from Hospices Civils de Lyon. The author has contributed to research in topics: Metabolism and Genetic Disorders & Lysosomal Storage Disorders Research & Mitochondrial Function and Pathology. The author has an h-index of 16, co-authored 41 publications.
Papers by this author
worksEfficacy and safety of i.v. sodium benzoate in urea cycle disorders: a multicentre retrospective study
2016 · Orphanet Journal of Rare Diseases · 40 citations
https://doi.org/10.1186/s13023-016-0513-0
Genotype-phenotype associations in French patients with phenylketonuria and importance of genotype for full assessment of tetrahydrobiopterin responsiveness
2015 · Orphanet Journal of Rare Diseases · 25 citations
https://doi.org/10.1186/s13023-015-0375-x
Treatment needs and expectations for Fabry disease in France: development of a new Patient Needs Questionnaire
2019 · Orphanet Journal of Rare Diseases · 7 citations
https://doi.org/10.1186/s13023-019-1254-7
Late-onset Fabry disease revealed by ventricular tachycardia: A case report
2021 · HeartRhythm Case Reports · 1 citations
https://doi.org/10.1016/j.hrcr.2021.11.025
Bone mineral density in French adults with early-treated phenylketonuria
2025 · Molecular Genetics and Metabolism · 1 citations
https://doi.org/10.1016/j.ymgme.2025.109044
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