Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

389 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
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: dulac o. Neurology. 2021 Mar 2;96(9):e1319-e1333. doi: 10.1212/WNL.0000000000011237. Epub 2020 Dec 4. Neurology. 2021. PMID: 33277420 Free PMC article.
STXBP1 germline mutation and focal cortical dysplasia.
Sharkov A, Dulac O, Gataullina S. Sharkov A, et al. Among authors: dulac o. Epileptic Disord. 2021 Feb 1;23(1):143-147. doi: 10.1684/epd.2021.1245. Epileptic Disord. 2021. PMID: 33632674
Seizure types and syndromes: lumping or splitting.
Dulac O, Guerrini R. Dulac O, et al. Epilepsy Res. 2001 May;45(1-3):37-40; discussion 41. doi: 10.1016/s0920-1211(01)00212-1. Epilepsy Res. 2001. PMID: 11461791 Review.
Epilepsy in inborn errors of metabolism.
Bahi-Buisson N, Dulac O. Bahi-Buisson N, et al. Among authors: dulac o. Handb Clin Neurol. 2013;111:533-41. doi: 10.1016/B978-0-444-52891-9.00056-7. Handb Clin Neurol. 2013. PMID: 23622201 Review.
From genotype to phenotype in Dravet disease.
Gataullina S, Dulac O. Gataullina S, et al. Among authors: dulac o. 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.
389 results