Ferrero G.B.; Baldassarre G.; Panza E.; Valenzise M.; Pippucci T.; Mussa A.; Pepe E.; Seri M.; Silengo M.C., A heritable cause of cleft lip and palate - Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis., «EUROPEAN JOURNAL OF PEDIATRICS», 2010, 169, pp. 223 - 228 [articolo]
Pippucci T.; Panza E.; Pompilii E.; Donadio V.; Borreca A.; Babalini C.; Patrono C.; Zuntini R.; Kawarai T.; Bernardi G.; Liguori R.; Romeo G.; Montagna P.; Orlacchio A.; Seri M., Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity., «EUROPEAN JOURNAL OF NEUROLOGY», 2009, 16, pp. 121 - 126 [articolo]
Panza E; Pippucci T; Cusano R; Lo Nigro C; Pradella L; Contardi S; Rouleau GA; Stevanin G; Ravazzolo R; Liguori R; Montagna P; Romeo G; Seri M., Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes., «EUROPEAN JOURNAL OF NEUROLOGY», 2008, 15(5), pp. 520 - 524 [articolo]
Deglincerti A; De Giorgio R; Cefle K; Devoto M; Pippucci T; Castegnaro G; Panza E; Barbara G; Cogliandro RF; Mungan Z; Palanduz S; Corinaldesi R; Romeo G; Seri M; Stanghellini V., A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24., «EUROPEAN JOURNAL OF HUMAN GENETICS», 2007, 15, pp. 889 - 897 [articolo]
