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23 results

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Page 1
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.
Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, LePiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria F, Annesi G, Striano S, Aguglia U, Guerrini R, Quattrone A. Annesi F, et al. Among authors: chifari r. Epilepsia. 2007 Sep;48(9):1686-1690. doi: 10.1111/j.1528-1167.2007.01173.x. Epub 2007 Jul 18. Epilepsia. 2007. PMID: 17634063 Free article.
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation.
Colosimo E, Gambardella A, Mantegazza M, Labate A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, Quattrone A. Colosimo E, et al. Among authors: chifari r. Epilepsia. 2007 Sep;48(9):1691-1696. doi: 10.1111/j.1528-1167.2007.01153.x. Epub 2007 Jun 12. Epilepsia. 2007. PMID: 17565594 Free article.
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy.
Gambardella A, Aguglia U, Chifari R, Labate A, Manna I, Serra P, Romeo N, Sibilia G, Lepiane E, Russa AL, Ventura P, Cittadella R, Sasanelli F, Colosimo E, Leggio U, Zappia M, Quattrone A. Gambardella A, et al. Among authors: chifari r. Epilepsia. 2005 Jan;46(1):110-7. doi: 10.1111/j.0013-9580.2005.15804.x. Epilepsia. 2005. PMID: 15660776 Free article.
Elderly people and epilepsy: cognitive function.
Piazzini A, Canevini MP, Turner K, Chifari R, Canger R. Piazzini A, et al. Among authors: chifari r. Epilepsia. 2006;47 Suppl 5:82-4. doi: 10.1111/j.1528-1167.2006.00884.x. Epilepsia. 2006. PMID: 17239113 Free article.
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Gambardella A, Manna I, Labate A, Chifari R, Serra P, La Russa A, LePiane E, Cittadella R, Andreoli V, Sasanelli F, Zappia M, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: chifari r. Epilepsia. 2003 Sep;44(9):1255-6. doi: 10.1046/j.1528-1157.2003.18003.x. Epilepsia. 2003. PMID: 12919401 Free article. No abstract available.
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures.
Mantegazza M, Gambardella A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Labate A, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, Quattrone A. Mantegazza M, et al. Among authors: chifari r. Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):18177-82. doi: 10.1073/pnas.0506818102. Epub 2005 Dec 2. Proc Natl Acad Sci U S A. 2005. PMID: 16326807 Free PMC article.
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy.
Gambardella A, Manna I, Labate A, Chifari R, La Russa A, Serra P, Cittadella R, Bonavita S, Andreoli V, LePiane E, Sasanelli F, Di Costanzo A, Zappia M, Tedeschi G, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: chifari r. Neurology. 2003 Feb 25;60(4):560-3. doi: 10.1212/01.wnl.0000046520.79877.d8. Neurology. 2003. PMID: 12601092
23 results