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Citation: M. Malacarne et al., Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity, AM J HU GEN, 68(6), 2001, pp. 1521-1526

Authors: Sander, T Schulz, H Saar, K Gennaro, E Riggio, MC Bianchi, A Zara, F Luna, D Bulteau, C Kaminska, A Ville, D Cieuta, C Picard, F Prud'homme, JF Bate, L Sundquist, A Gardiner, RM Janssen, GAMAJ de Haan, GJ Kasteleijn-Nolst-Trenite, DGA Bader, A Lindhout, D Riess, O Wienker, TF Janz, D Reis, A

Citation: T. Sander et al., Genome search for susceptibility loci of common idiopathic generalised epilepsies, HUM MOL GEN, 9(10), 2000, pp. 1465-1472

Authors: Zara, F Gennaro, E Stabile, M Carbone, I Malacarne, M Majello, L Santangelo, R de Falco, FA Bricarelli, FD

Citation: F. Zara et al., Mapping of a locus for a familial autosomal recessive idiopathic myoclonicepilepsy of infancy to chromosome 16p13, AM J HU GEN, 66(5), 2000, pp. 1552-1557

Authors: Gennaro, E Malacarne, M Carbone, I Riggio, MC Bianchi, A Bonanni, P Boniver, C Dalla Bernardina, B De Marco, P Giordano, L Guerrini, R Santorum, E Sebastianelli, R Vecchi, M Veggiotti, P Vigevano, F Bricarelli, FD Zara, F

Citation: E. Gennaro et al., No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1, EPILEPSIA, 40(12), 1999, pp. 1799-1803