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Page 1
Ipilimumab-induced renal granulomatous arteritis: a case report.
Lemoine M, Dilly B, Curie A, Hébert V, Laurent C, Hanoy M, Grangé S, Guerrot D, François A, Bertrand D. Lemoine M, et al. Among authors: curie a. BMC Nephrol. 2019 Oct 11;20(1):366. doi: 10.1186/s12882-019-1552-2. BMC Nephrol. 2019. PMID: 31604452 Free PMC article.
Effet indésirable rare d’un anti-IL-1RA.
Brevet P, Curie A, Princivil C, Zarnitsky C, Boulay C, Alcaix D. Brevet P, et al. Among authors: curie a. Rev Med Interne. 2020 May;41(5):343-345. doi: 10.1016/j.revmed.2019.11.008. Epub 2019 Dec 6. Rev Med Interne. 2020. PMID: 31818504 French.
A phase II double-blind multicentre, placebo-controlled trial to assess the efficacy and safety of alpelisib (BYL719) in paediatric and adult patients with Megalencephaly-CApillary malformation Polymicrogyria syndrome (MCAP): the SESAM study protocol.
Luu M, Vabres P, Espitalier A, Maurer A, Garde A, Racine C, Carpentier M, Rega A, Loffroy R, Hadouiri N, Boddaert N, Curie A, Guibaud L, Chebbi M, Charligny J, Kuentz P, Canaud G, Bahi-Buisson N, Fleck C, Cransac A, Bardou M, Faivre L; SESAM study group. Luu M, et al. Among authors: curie a. BMJ Open. 2024 Dec 20;14(12):e084614. doi: 10.1136/bmjopen-2024-084614. BMJ Open. 2024. PMID: 39806603 Free PMC article. Clinical Trial.
Central nervous system vasculitis in VEXAS syndrome: A rare involvemen.
Langlois V, Curie A, Demas A, Etancelin P, Sauvètre G, Leclancher A, Mekinian A. Langlois V, et al. Among authors: curie a. Clin Neurol Neurosurg. 2024 Jul;242:108351. doi: 10.1016/j.clineuro.2024.108351. Epub 2024 May 23. Clin Neurol Neurosurg. 2024. PMID: 38801808
Clinical Characteristics, Developmental Trajectory, and Caregiver Burden of Patients With Creatine Transporter Deficiency (SLC6A8).
Curie A, Lion-François L, Valayannopoulos V, Perreton N, Gavanon M, Touil N, Brun-Laurisse A, Gheurbi F, Buchy M, Halep H, Cheillan D, Mercier C, Brassier A, Desnous B, Kassai B, De Lonlay P, Des Portes V. Curie A, et al. Neurology. 2024 Apr 23;102(8):e209243. doi: 10.1212/WNL.0000000000209243. Epub 2024 Mar 26. Neurology. 2024. PMID: 38531017
Further characterisation of ARX-related disorders in females due to inherited or de novo variants.
Gras M, Heide S, Keren B, Valence S, Garel C, Whalen S, Jansen AC, Keymolen K, Stouffs K, Jennesson M, Poirsier C, Lesca G, Depienne C, Nava C, Rastetter A, Curie A, Cuisset L, Des Portes V, Milh M, Charles P, Mignot C, Héron D. Gras M, et al. Among authors: curie a. J Med Genet. 2024 Jan 19;61(2):103-108. doi: 10.1136/jmg-2023-109203. J Med Genet. 2024. PMID: 37879892 Review.
Extending the phenotypes associated with TRIO gene variants in a cohort of 25 patients and review of the literature.
Gazdagh G, Hunt D, Gonzalez AMC, Rodriguez MP, Chaudhry A, Madruga M, Vansenne F, Shears D, Curie A, Stattin EL, Anderlid BM, Trajkova S, Angelovska ES, McWilliam C, Wyatt PR, O'Driscoll M, Atton G, Bergman AK, Zacher P, Mewasingh LD, López AG, Alonso-Luengo O, Wai HA, Rohde O, Boiroux P, Debant A, Schmidt S, Baralle D. Gazdagh G, et al. Among authors: curie a. Am J Med Genet A. 2023 Jul;191(7):1722-1740. doi: 10.1002/ajmg.a.63194. Epub 2023 Mar 29. Am J Med Genet A. 2023. PMID: 36987741 Review.
Placebo effects in children with autism spectrum disorder.
Curie A, Oberlander TF, Jensen KB. Curie A, et al. Dev Med Child Neurol. 2023 Oct;65(10):1316-1320. doi: 10.1111/dmcn.15574. Epub 2023 Mar 14. Dev Med Child Neurol. 2023. PMID: 36917698 Free article. Review.
41 results