Granata T - Search Results

1

Band heterotopia: correlation of outcome with magnetic resonance imaging parameters.

Barkovich AJ, Guerrini R, Battaglia G, Kalifa G, N'Guyen T, Parmeggiani A, Santucci M, Giovanardi-Rossi P, Granata T, D'Incerti L. Barkovich AJ, et al. Among authors: granata t. Ann Neurol. 1994 Oct;36(4):609-17. doi: 10.1002/ana.410360409. Ann Neurol. 1994. PMID: 7524438

2

Double cortex syndrome: electroclinical study of three cases.

Granata T, Battaglia G, D'Incerti L, Franceschetti S, Zucca C, Savoiardo M, Avanzini G. Granata T, et al. Ital J Neurol Sci. 1994 Feb;15(1):15-23. doi: 10.1007/BF02343493. Ital J Neurol Sci. 1994. PMID: 8206743

3

Schizencephaly: neuroradiologic and epileptologic findings.

Granata T, Battaglia G, D'Incerti L, Franceschetti S, Spreafico R, Battino D, Savoiardo M, Avanzini G. Granata T, et al. Epilepsia. 1996 Dec;37(12):1185-93. doi: 10.1111/j.1528-1157.1996.tb00551.x. Epilepsia. 1996. PMID: 8956850

4

Neuronal migration disorders and epilepsy: a morphological analysis of three surgically treated patients.

Battaglia G, Arcelli P, Granata T, Selvaggio M, Andermann F, Dubeau F, Olivier A, Tampieri D, Villemure JG, Avoli M, Avanzini G, Spreafico R. Battaglia G, et al. Among authors: granata t. Epilepsy Res. 1996 Dec;26(1):49-58. doi: 10.1016/s0920-1211(96)00039-3. Epilepsy Res. 1996. PMID: 8985686

5

Familial schizencephaly associated with EMX2 mutation.

Granata T, Farina L, Faiella A, Cardini R, D'Incerti L, Boncinelli E, Battaglia G. Granata T, et al. Neurology. 1997 May;48(5):1403-6. doi: 10.1212/wnl.48.5.1403. Neurology. 1997. PMID: 9153481

6

A number of schizencephaly patients including 2 brothers are heterozygous for germline mutations in the homeobox gene EMX2.

Faiella A, Brunelli S, Granata T, D'Incerti L, Cardini R, Lenti C, Battaglia G, Boncinelli E. Faiella A, et al. Among authors: granata t. Eur J Hum Genet. 1997 Jul-Aug;5(4):186-90. Eur J Hum Genet. 1997. PMID: 9359037

7

Periventricular nodular heterotopia: epileptogenic findings.

Battaglia G, Granata T, Farina L, D'Incerti L, Franceschetti S, Avanzini G. Battaglia G, et al. Among authors: granata t. Epilepsia. 1997 Nov;38(11):1173-82. doi: 10.1111/j.1528-1157.1997.tb01213.x. Epilepsia. 1997. PMID: 9579917 Free article.

8

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.

Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F. Nabbout R, et al. Among authors: granata t. Neurology. 2003 Jun 24;60(12):1961-7. doi: 10.1212/01.wnl.0000069463.41870.2f. Neurology. 2003. PMID: 12821740

9

Epileptic and imaging findings in perinatal hypoxic-ischemic encephalopathy with ulegyria.

Villani F, D'Incerti L, Granata T, Battaglia G, Vitali P, Chiapparini L, Avanzini G. Villani F, et al. Among authors: granata t. Epilepsy Res. 2003 Aug;55(3):235-43. doi: 10.1016/s0920-1211(03)00121-9. Epilepsy Res. 2003. PMID: 12972177

10

Schizencephaly: clinical spectrum, epilepsy, and pathogenesis.

Granata T, Freri E, Caccia C, Setola V, Taroni F, Battaglia G. Granata T, et al. J Child Neurol. 2005 Apr;20(4):313-8. doi: 10.1177/08830738050200040801. J Child Neurol. 2005. PMID: 15921232 Review.

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