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

60 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, Vanni N, Beccaria F, Capovilla G, Bianchi A, Caffi L, Cardilli V, Darra F, Bernardina BD, Fusco L, Gaggero R, Giordano L, Guerrini R, Incorpora G, Mastrangelo M, Spaccini L, Laverda AM, Vecchi M, Vanadia F, Veggiotti P, Viri M, Occhi G, Budetta M, Taglialatela M, Coviello DA, Vigevano F, Minetti C. Zara F, et al. Among authors: bernardina bd. Epilepsia. 2013 Mar;54(3):425-36. doi: 10.1111/epi.12089. Epub 2013 Jan 29. Epilepsia. 2013. PMID: 23360469 Free article.
Lack of SCN1A mutations in familial febrile seizures.
Malacarne M, Madia F, Gennaro E, Vacca D, Güney AI, Buono S, Bernardina BD, Gaggero R, Gobbi G, Lispi ML, Malamaci D, Melideo G, Roccella M, Sferro C, Tiberti A, Vanadia F, Vigevano F, Viri F, Vitali MR, Bricarelli FD, Bianchi A, Zara F. Malacarne M, et al. Among authors: bernardina bd. Epilepsia. 2002 May;43(5):559-62. doi: 10.1046/j.1528-1157.2002.29301.x. Epilepsia. 2002. PMID: 12027919 Free article.
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.
Specchio N, Marini C, Terracciano A, Mei D, Trivisano M, Sicca F, Fusco L, Cusmai R, Darra F, Bernardina BD, Bertini E, Guerrini R, Vigevano F. Specchio N, et al. Among authors: bernardina bd. Epilepsia. 2011 Jul;52(7):1251-7. doi: 10.1111/j.1528-1167.2011.03063.x. Epub 2011 Apr 11. Epilepsia. 2011. PMID: 21480887 Free article.
Early-onset absence epilepsy and paroxysmal dyskinesia.
Guerrini R, Sanchez-Carpintero R, Deonna T, Santucci M, Bhatia KP, Moreno T, Parmeggiani L, Bernardina BD. Guerrini R, et al. Among authors: bernardina bd. Epilepsia. 2002 Oct;43(10):1224-9. doi: 10.1046/j.1528-1157.2002.13802.x. Epilepsia. 2002. PMID: 12366739 Free article.
Temporal lobe epilepsy in children: electroclinical study of 77 cases.
Fontana E, Negrini F, Francione S, Mai R, Osanni E, Menna E, Offredi F, Darra F, Bernardina BD. Fontana E, et al. Among authors: bernardina bd. Epilepsia. 2006;47 Suppl 5:26-30. doi: 10.1111/j.1528-1167.2006.00873.x. Epilepsia. 2006. PMID: 17239102 Free article.
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life.
Battaglia D, Chieffo D, Lucibello S, Marini C, Sibilia V, Mei D, Darra F, Offredi F, Fontana E, Specchio N, Cappelletti S, Granata T, Ragona F, Patrini M, Baglietto MG, Prato G, Ferrari A, Vigevano F, Mercuri E, Bernardina BD, Guerrini R, Dravet C, Guzzetta F. Battaglia D, et al. Among authors: bernardina bd. Brain Dev. 2021 Mar;43(3):419-430. doi: 10.1016/j.braindev.2020.10.004. Epub 2021 Jan 18. Brain Dev. 2021. PMID: 33478845
60 results