Guerrini R - Search Results

1

Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 Encephalopathy.

Lenge M, Marini C, Canale E, Napolitano A, De Masi S, Trivisano M, Mei D, Longo D, Rossi Espagnet MC, Lucenteforte E; PCDH19 Clinical Study Group; Barba C, Specchio N, Guerrini R. Lenge M, et al. Among authors: guerrini r. Cereb Cortex. 2020 Oct 1;30(11):6039-6050. doi: 10.1093/cercor/bhaa177. Cereb Cortex. 2020. PMID: 32582916

2

Autosomal recessive polymicrogyria with infantile spasms and limb deformities.

Ciardo F, Zamponi N, Specchio N, Parmeggiani L, Guerrini R. Ciardo F, et al. Among authors: guerrini r. Neuropediatrics. 2001 Dec;32(6):325-9. doi: 10.1055/s-2001-20409. Neuropediatrics. 2001. PMID: 11870589

3

The genetic and molecular basis of epilepsy.

Guerrini R, Casari G, Marini C. Guerrini R, et al. Trends Mol Med. 2003 Jul;9(7):300-6. doi: 10.1016/s1471-4914(03)00116-3. Trends Mol Med. 2003. PMID: 12900217 Review.

4

Mosaic mutations of the LIS1 gene cause subcortical band heterotopia.

Sicca F, Kelemen A, Genton P, Das S, Mei D, Moro F, Dobyns WB, Guerrini R. Sicca F, et al. Among authors: guerrini r. Neurology. 2003 Oct 28;61(8):1042-6. doi: 10.1212/wnl.61.8.1042. Neurology. 2003. PMID: 14581661

5

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: guerrini r. Epilepsia. 2004 Feb;45(2):149-58. doi: 10.1111/j.0013-9580.2004.04303.x. Epilepsia. 2004. PMID: 14738422 Free article.

6

Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopia.

Parrini E, Mei D, Wright M, Dorn T, Guerrini R. Parrini E, et al. Among authors: guerrini r. Neurogenetics. 2004 Sep;5(3):191-6. doi: 10.1007/s10048-004-0187-y. Epub 2004 Jul 28. Neurogenetics. 2004. PMID: 15459826

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. 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: guerrini r. Epilepsia. 2005 Jan;46(1):118-23. doi: 10.1111/j.0013-9580.2005.26304.x. Epilepsia. 2005. PMID: 15660777 Free article.

9

Resective surgery for epileptogenic dysembryoplastic neuroepithelial tumor in hemimegalencephaly.

Specchio N, Kahane P, Pasquier B, Tassi L, Guerrini R. Specchio N, et al. Among authors: guerrini r. Neurology. 2005 Sep 13;65(5):777-8. doi: 10.1212/01.wnl.0000174627.76924.0c. Neurology. 2005. PMID: 16157925 No abstract available.

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. Among authors: guerrini r. J Child Neurol. 2005 Aug;20(8):693-6. doi: 10.1177/08830738050200081201. J Child Neurol. 2005. PMID: 16225818

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