Marini C - Search Results

1

Marini C, Scheffer IE, Nabbout R, Suls A, De Jonghe P, Zara F, Guerrini R. Marini C, et al. Epilepsia. 2011 Apr;52 Suppl 2:24-9. doi: 10.1111/j.1528-1167.2011.02997.x. Epilepsia. 2011. PMID: 21463275 Free article. Review.

2

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.

Marini C, Harkin LA, Wallace RH, Mulley JC, Scheffer IE, Berkovic SF. Marini C, et al. Brain. 2003 Jan;126(Pt 1):230-40. doi: 10.1093/brain/awg018. Brain. 2003. PMID: 12477709

3

Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.

Bonanni P, Malcarne M, Moro F, Veggiotti P, Buti D, Ferrari AR, Parrini E, Mei D, Volzone A, Zara F, Heron SE, Bordo L, Marini C, Guerrini R. Bonanni P, et al. Among authors: marini c. Epilepsia. 2004 Feb;45(2):149-58. doi: 10.1111/j.0013-9580.2004.04303.x. Epilepsia. 2004. PMID: 14738422 Free article.

4

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.

Berkovic SF, Heron SE, Giordano L, Marini C, Guerrini R, Kaplan RE, Gambardella A, Steinlein OK, Grinton BE, Dean JT, Bordo L, Hodgson BL, Yamamoto T, Mulley JC, Zara F, Scheffer IE. Berkovic SF, et al. Among authors: marini c. Ann Neurol. 2004 Apr;55(4):550-7. doi: 10.1002/ana.20029. Ann Neurol. 2004. PMID: 15048894

5

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF. Marini C, et al. Epilepsia. 2004 May;45(5):467-78. doi: 10.1111/j.0013-9580.2004.46803.x. Epilepsia. 2004. PMID: 15101828 Free article.

6

Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?

Taylor I, Marini C, Johnson MR, Turner S, Berkovic SF, Scheffer IE. Taylor I, et al. Among authors: marini c. Brain. 2004 Aug;127(Pt 8):1878-86. doi: 10.1093/brain/awh211. Epub 2004 Jun 16. Brain. 2004. PMID: 15201194

7

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Parmeggiani L, Marini C, Brovedani P, Bonanni P. Guerrini R, et al. Among authors: marini c. Adv Neurol. 2005;95:273-9. Adv Neurol. 2005. PMID: 15508930 No abstract available.

8

Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation.

Pisano T, Marini C, Brovedani P, Brizzolara D, Pruna D, Mei D, Moro F, Cianchetti C, Guerrini R. Pisano T, et al. Among authors: marini c. Epilepsia. 2005 Jan;46(1):118-23. doi: 10.1111/j.0013-9580.2005.26304.x. Epilepsia. 2005. PMID: 15660777 Free article.

9

No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures.

Martinelli Boneschi F, Aridon P, Zara F, Guerrini R, Marini C, De Fusco M, Comi G, Casari G. Martinelli Boneschi F, et al. Among authors: marini c. Neurosci Lett. 2005 Nov 11;388(2):71-4. doi: 10.1016/j.neulet.2005.06.026. Neurosci Lett. 2005. PMID: 16026932

10

Nonconvulsive status epilepticus precipitated by carbamazepine presenting as dissociative and affective disorders in adolescents.

Marini C, Parmeggiani L, Masi G, D'Arcangelo G, Guerrini R. Marini C, et al. J Child Neurol. 2005 Aug;20(8):693-6. doi: 10.1177/08830738050200081201. J Child Neurol. 2005. PMID: 16225818

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