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"Alternating" the Diagnosis after 40 Years of Disease: The Thousand Faces of ATP1A3 Mutation.
Mov Disord Clin Pract. 2024 Aug;11 Suppl 2(Suppl 2):S11-S13. doi: 10.1002/mdc3.13980. Epub 2024 Jan 22.
Mov Disord Clin Pract. 2024.
PMID: 38247386
Free PMC article.
No abstract available.
Long-term outcomes of paediatric Guillain-Barré syndrome.
Estublier B, Colineaux H, Arnaud C, Cintas P, Baudou E, Chaix Y, Rivier F, Biotteau M, Meyer P, Cheuret E.
Estublier B, et al.
Dev Med Child Neurol. 2024 Feb;66(2):176-186. doi: 10.1111/dmcn.15693. Epub 2023 Jul 27.
Dev Med Child Neurol. 2024.
PMID: 37501281
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Unusual circumstance for craniopharyngioma discovery on meningoencephalitis: a pediatric case report.
Oozeerally J, Berthomieu L, Bertozzi AI, Estublier B, Oliver I, Siegfried A, Antherieu P, Thene E, Jamme T, Levade T, Sevely A, Brehin C, Baudou E.
Oozeerally J, et al. Among authors: estublier b.
BMC Pediatr. 2023 Mar 22;23(1):132. doi: 10.1186/s12887-023-03930-5.
BMC Pediatr. 2023.
PMID: 36949415
Free PMC article.
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Cerliponase alfa changes the natural history of children with neuronal ceroid lipofuscinosis type 2: The first French cohort.
Estublier B, Cano A, Hoebeke C, Pichard S, Scavarda D, Desguerre I, Auvin S, Chabrol B.
Estublier B, et al.
Eur J Paediatr Neurol. 2021 Jan;30:17-21. doi: 10.1016/j.ejpn.2020.12.002. Epub 2020 Dec 8.
Eur J Paediatr Neurol. 2021.
PMID: 33348105
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