11 results for author:"Granata T." in Literature citations
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| Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. Marini C., Darra F., Specchio N., Mei D., Terracciano A., Parmeggiani L., Ferrari A., Sicca F., Mastrangelo M., Spaccini L. et al. Epilepsia 53:2111-2119(2012) · Mapped (3) |
| De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Heinzen E.L., Swoboda K.J., Hitomi Y., Gurrieri F., Nicole S., de Vries B., Tiziano F.D., Fontaine B., Walley N.M., Heavin S. et al. Nat. Genet. 44:1030-1034(2012) · UniProtKB (1) · Mapped (11) |
| West syndrome associated with 14q12 duplications harboring FOXG1. Striano P., Paravidino R., Sicca F., Chiurazzi P., Gimelli S., Coppola A., Robbiano A., Traverso M., Pintaudi M., Giovannini S. et al. Neurology 76:1600-1602(2011) · Mapped (1) |
| Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy. Busolin G., Malacrida S., Bisulli F., Striano P., Di Bonaventura C., Egeo G., Pasini E., Cianci V., Ferlazzo E., Bianchi A. et al. Epilepsy Res. 94:110-116(2011) · Mapped (4) |
| Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathy. Mei D., Marini C., Novara F., Bernardina B.D., Granata T., Fontana E., Parrini E., Ferrari A.R., Murgia A., Zuffardi O. et al. Epilepsia 51:647-654(2010) · Mapped (1) |
| Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6. Cannelli N., Garavaglia B., Simonati A., Aiello C., Barzaghi C., Pezzini F., Cilio M.R., Biancheri R., Morbin M., Dalla Bernardina B. et al. Biochem. Biophys. Res. Commun. 379:892-897(2009) · Mapped (5) |
| Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis. Cannelli N., Nardocci N., Cassandrini D., Morbin M., Aiello C., Bugiani M., Criscuolo L., Zara F., Striano P., Granata T. et al. |
| Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. Mancardi M.M., Striano P., Gennaro E., Madia F., Paravidino R., Scapolan S., Dalla Bernardina B., Bertini E., Bianchi A., Capovilla G. et al. |
| Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy. Gennaro E., Santorelli F.M., Bertini E., Buti D., Gaggero R., Gobbi G., Lini M., Granata T., Freri E., Parmeggiani A. et al. Biochem. Biophys. Res. Commun. 341:489-493(2006) · Mapped (7) |
| 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. et al. |
| No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy. Madia F., Gennaro E., Cecconi M., Buti D., Capovilla G., Dalla Bernardina B., Elia M., Ferrari A., Fontana E., Gaggero R. et al. Epilepsy Res. 53:196-200(2003) · Mapped (3) |