Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients
2015 · Orphanet Journal of Rare Diseases · 152 citations
https://doi.org/10.1186/s13023-015-0335-5
M
Michela Stagnaro
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
30
Papers
821
Citations
10
h-index
10
i10-index
Michela Stagnaro is an academic researcher from Istituto Giannina Gaslini. The author has contributed to research in topics: Neurogenetic and Muscular Disorders Research & Genomics and Rare Diseases & Hereditary Neurological Disorders. The author has an h-index of 10, co-authored 26 publications.
ORCID: 0000-0002-7041-2858Papers by this author
worksIdentification of a rare 17p13.3 duplication including the BHLHA9 and YWHAEgenes in a family with developmental delay and behavioural problems
2012 · BMC Medical Genetics · 40 citations
https://doi.org/10.1186/1471-2350-13-93
Practical management of repeated life‐threatening status epilepticus in Alternating Hemiplegia of Childhood: Case report and literature review
2025 · Epileptic Disorders · 0 citations
https://doi.org/10.1002/epd2.70031
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat