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The ENIGMA-Epilepsy working group: Mapping disease from large data sets.
Sisodiya SM, Whelan CD, Hatton SN, Huynh K, Altmann A, Ryten M, Vezzani A, Caligiuri ME, Labate A, Gambardella A, Ives-Deliperi V, Meletti S, Munsell BC, Bonilha L, Tondelli M, Rebsamen M, Rummel C, Vaudano AE, Wiest R, Balachandra AR, Bargalló N, Bartolini E, Bernasconi A, Bernasconi N, Bernhardt B, Caldairou B, Carr SJA, Cavalleri GL, Cendes F, Concha L, Desmond PM, Domin M, Duncan JS, Focke NK, Guerrini R, Hamandi K, Jackson GD, Jahanshad N, Kälviäinen R, Keller SS, Kochunov P, Kowalczyk MA, Kreilkamp BAK, Kwan P, Lariviere S, Lenge M, Lopez SM, Martin P, Mascalchi M, Moreira JCV, Morita-Sherman ME, Pardoe HR, Pariente JC, Raviteja K, Rocha CS, Rodríguez-Cruces R, Seeck M, Semmelroch MKHG, Sinclair B, Soltanian-Zadeh H, Stein DJ, Striano P, Taylor PN, Thomas RH, Thomopoulos SI, Velakoulis D, Vivash L, Weber B, Yasuda CL, Zhang J, Thompson PM, McDonald CR; ENIGMA Consortium Epilepsy Working Group. Sisodiya SM, et al. Among authors: guerrini r. Hum Brain Mapp. 2020 May 29;43(1):113-28. doi: 10.1002/hbm.25037. Online ahead of print. Hum Brain Mapp. 2020. PMID: 32468614 Free PMC article. Review.
Neuroimaging and neuropathology of Dravet syndrome.
Guerrini R, Striano P, Catarino C, Sisodiya SM. Guerrini R, et al. Epilepsia. 2011 Apr;52 Suppl 2:30-4. doi: 10.1111/j.1528-1167.2011.02998.x. Epilepsia. 2011. PMID: 21463276 Free article. Review.
Atypical face shape and genomic structural variants in epilepsy.
Chinthapalli K, Bartolini E, Novy J, Suttie M, Marini C, Falchi M, Fox Z, Clayton LM, Sander JW, Guerrini R, Depondt C, Hennekam R, Hammond P, Sisodiya SM. Chinthapalli K, et al. Among authors: guerrini r. Brain. 2012 Oct;135(Pt 10):3101-14. doi: 10.1093/brain/aws232. Epub 2012 Sep 13. Brain. 2012. PMID: 22975390 Free PMC article.
The α2B-adrenergic receptor is mutant in cortical myoclonus and epilepsy.
De Fusco M, Vago R, Striano P, Di Bonaventura C, Zara F, Mei D, Kim MS, Muallem S, Chen Y, Wang Q, Guerrini R, Casari G. De Fusco M, et al. Among authors: guerrini r. Ann Neurol. 2014 Jan;75(1):77-87. doi: 10.1002/ana.24028. Epub 2014 Jan 2. Ann Neurol. 2014. PMID: 24114805 Free PMC article.
Co-occurring malformations of cortical development and SCN1A gene mutations.
Barba C, Parrini E, Coras R, Galuppi A, Craiu D, Kluger G, Parmeggiani A, Pieper T, Schmitt-Mechelke T, Striano P, Giordano F, Blumcke I, Guerrini R. Barba C, et al. Among authors: guerrini r. Epilepsia. 2014 Jul;55(7):1009-19. doi: 10.1111/epi.12658. Epub 2014 Jun 5. Epilepsia. 2014. PMID: 24902755 Free article.
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
Mumoli L, Tarantino P, Michelucci R, Bianchi A, Labate A, Franceschetti S, Marini C, Striano P, Gagliardi M, Ferlazzo E, Sofia V, Pennese L, Annesi G, Aguglia U, Guerrini R, Zara F, Gambardella A; Genetic Commission, Italian League Against Epilepsy. Mumoli L, et al. Among authors: guerrini r. Epilepsia. 2015 Apr;56(4):e40-3. doi: 10.1111/epi.12944. Epub 2015 Mar 6. Epilepsia. 2015. PMID: 25752200 Free article.
7T MRI in focal epilepsy with unrevealing conventional field strength imaging.
De Ciantis A, Barba C, Tassi L, Cosottini M, Tosetti M, Costagli M, Bramerio M, Bartolini E, Biagi L, Cossu M, Pelliccia V, Symms MR, Guerrini R. De Ciantis A, et al. Among authors: guerrini r. Epilepsia. 2016 Mar;57(3):445-54. doi: 10.1111/epi.13313. Epub 2016 Jan 18. Epilepsia. 2016. PMID: 26778405 Free article.
1,080 results