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Page 1
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome.
Masnada S, Pichiecchio A, Formica M, Arrigoni F, Borrelli P, Accorsi P, Bonanni P, Borgatti R, Bernardina BD, Danieli A, Darra F, Deconinck N, De Giorgis V, Dulac O, Gataullina S, Giordano L, Guerrini R, La Briola F, Mastrangelo M, Montomoli M, Mortilla M, Osanni E, Parisi P, Perucca E, Pinelli L, Romaniello R, Severino M, Vigevano F, Vignoli A, Bahi-Buisson N, Cavallin M, Accogli A, Burgeois M, Capra V, Chaves-Vischer V, Chiapparini L, Colafati G, D'Arrigo S, Desguerre I, Doco-Fenzy M, d'Orsi G, Epitashvili N, Fazzi E, Ferretti A, Fiorini E, Fradin M, Fusco C, Granata T, Johannesen KM, Lebon S, Loget P, Moller RS, Montanaro D, Orcesi S, Quelin C, Rebessi E, Romeo A, Solazzi R, Spagnoli C, Uebler C, Zara F, Arzimanoglou A, Veggiotti P; Aicardi Syndrome International Study Group. Masnada S, et al. Among authors: gataullina s. Neurology. 2021 Mar 2;96(9):e1319-e1333. doi: 10.1212/WNL.0000000000011237. Epub 2020 Dec 4. Neurology. 2021. PMID: 33277420 Free PMC article.
Early electro-clinical features may contribute to diagnosis of the anti-NMDA receptor encephalitis in children.
Gitiaux C, Simonnet H, Eisermann M, Leunen D, Dulac O, Nabbout R, Chevignard M, Honnorat J, Gataullina S, Musset L, Scalais E, Gauthier A, Hully M, Boddaert N, Kuchenbuch M, Desguerre I, Kaminska A. Gitiaux C, et al. Among authors: gataullina s. Clin Neurophysiol. 2013 Dec;124(12):2354-61. doi: 10.1016/j.clinph.2013.05.023. Epub 2013 Jul 2. Clin Neurophysiol. 2013. PMID: 23830005
Temporal lobe epilepsy in infants and children.
Gataullina S, Dulac O, Bulteau C. Gataullina S, et al. Rev Neurol (Paris). 2015 Mar;171(3):252-8. doi: 10.1016/j.neurol.2015.01.559. Epub 2015 Mar 2. Rev Neurol (Paris). 2015. PMID: 25744768 Review.
Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.
Gataullina S, Lemaire E, Wendling F, Kaminska A, Watrin F, Riquet A, Ville D, Moutard ML, de Saint Martin A, Napuri S, Pedespan JM, Eisermann M, Bahi-Buisson N, Nabbout R, Chiron C, Dulac O, Huberfeld G. Gataullina S, et al. Epilepsia. 2016 Apr;57(4):648-59. doi: 10.1111/epi.13325. Epub 2016 Feb 13. Epilepsia. 2016. PMID: 26873267 Free article.
From genotype to phenotype in Dravet disease.
Gataullina S, Dulac O. Gataullina S, et al. Seizure. 2017 Jan;44:58-64. doi: 10.1016/j.seizure.2016.10.014. Epub 2016 Oct 21. Seizure. 2017. PMID: 27817982 Free article. Review.
Is epilepsy the cause of comorbidities in Dravet syndrome?
Gataullina S, Dulac O. Gataullina S, et al. Dev Med Child Neurol. 2018 Jan;60(1):8. doi: 10.1111/dmcn.13613. Epub 2017 Nov 10. Dev Med Child Neurol. 2018. PMID: 29124748 Free article. No abstract available.
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