Disease manifestations and burden of illness in patients with acid sphingomyelinase deficiency (ASMD)
2017 · Orphanet Journal of Rare Diseases · 171 citations
https://doi.org/10.1186/s13023-017-0572-x
O
Olivier Lidove
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Olivier Lidove is an academic researcher from Groupe Hospitalier Diaconesses Croix Saint-Simon. The author has contributed to research in topics: Lysosomal Storage Disorders Research & Glycogen Storage Diseases and Myoclonus & Trypanosoma species research and implications. The author has an h-index of 37, co-authored 267 publications.
ORCID: 0000-0003-4847-7839Papers by this author
worksConsensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency
2017 · Genetics in Medicine · 110 citations
https://doi.org/10.1038/gim.2017.7
A randomized, placebo-controlled clinical trial evaluating olipudase alfa enzyme replacement therapy for chronic acid sphingomyelinase deficiency (ASMD) in adults: One-year results
2022 · Genetics in Medicine · 91 citations
https://doi.org/10.1016/j.gim.2022.03.021
Continued improvement in disease manifestations of acid sphingomyelinase deficiency for adults with up to 2 years of olipudase alfa treatment: open-label extension of the ASCEND trial
2023 · Orphanet Journal of Rare Diseases · 20 citations
https://doi.org/10.1186/s13023-023-02983-0
Fabry in the older patient: Clinical consequences and possibilities for treatment
2016 · Molecular Genetics and Metabolism · 17 citations
https://doi.org/10.1016/j.ymgme.2016.05.009
Streptococcal and Staphylococcus aureus prosthetic joint infections: are they really different?
2022 · BMC Infectious Diseases · 17 citations
https://doi.org/10.1186/s12879-022-07532-x
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