12 results for author:"Gennaro E." in Literature citations
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| Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations. Canafoglia L., Gennaro E., Capovilla G., Gobbi G., Boni A., Beccaria F., Viri M., Michelucci R., Agazzi P., Assereto S. et al. Epilepsia 53:2120-2127(2012) · Mapped (2) |
| Fever as a seizure precipitant factor in Panayiotopoulos syndrome: a clinical and genetic study. Cordelli D.M., Aldrovandi A., Gentile V., Garone C., Conti S., Aceti A., Gennaro E., Zara F., Franzoni E. Seizure 21:141-143(2012) · Mapped (7) |
| Kita driven expression of oncogenic HRAS leads to early onset and highly penetrant melanoma in zebrafish. Santoriello C., Gennaro E., Anelli V., Distel M., Kelly A., Koster R.W., Hurlstone A., Mione M. PLoS ONE 5:e15170-e15170(2010) · Mapped (8) |
| Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy). Nicita F., Spalice A., Papetti L., Ursitti F., Parisi P., Gennaro E., Zara F., Iannetti P. J. Child Neurol. 25:1369-1376(2010) · UniProtKB (1) |
| SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis. Marini C., Scheffer I.E., Nabbout R., Mei D., Cox K., Dibbens L.M., McMahon J.M., Iona X., Carpintero R.S., Elia M. et al. Epilepsia 50:1670-1678(2009) · Mapped (7) |
| 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. |
| Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy. Madia F., Striano P., Gennaro E., Malacarne M., Paravidino R., Biancheri R., Budetta M., Cilio M.R., Gaggero R., Pierluigi M. et al. Neurology 67:1230-1235(2006) · Mapped (7) |
| 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. |
| Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity. Gennaro E., Veggiotti P., Malacarne M., Madia F., Cecconi M., Cardinali S., Cassetti A., Cecconi I., Bertini E., Bianchi A. et al. Epileptic Disord 5:21-25(2003) · Mapped (7) |
| 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) |
| Critical role of both p27KIP1 and p21CIP1/WAF1 in the antiproliferative effect of ZD1839 ('Iressa'), an epidermal growth factor receptor tyrosine kinase inhibitor, in head and neck squamous carcinoma cells. Di Gennaro E., Barbarino M., Bruzzese F., De Lorenzo S., Caraglia M., Abbruzzese A., Avallone A., Comella P., Caponigro F., Pepe S. et al. J. Cell. Physiol. 195:139-150(2003) · Mapped (8) |