Charles H. Knowles;Greger Lindberg;Emanuele Panza;Roberto De Giorgio, New perspectives in the diagnosis and management of enteric neuropathies, «NATURE REVIEWS. GASTROENTEROLOGY & HEPATOLOGY», 2013, 10, pp. 206 - 218 [articolo]
Panza E; Knowles CH; Graziano C; Thapar N; Burns AJ; Seri M; Stanghellini V; De Giorgio R., Genetics of human enteric neuropathies., «PROGRESS IN NEUROBIOLOGY», 2012, 96, pp. 176 - 189 [articolo]
Pecci A.; Bozzi V.; Panza E.; Barozzi S.; Gruppi C.; Seri M.; Balduini C.L., Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells, «THROMBOSIS AND HAEMOSTASIS», 2011, 106, pp. 693 - 704 [articolo]
Pecci A; Bozzi V; Panza E; Barozzi S; Gruppi C; Seri M; Balduini CL., Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells., «THROMBOSIS AND HAEMOSTASIS», 2011, 106, pp. 693 - 704 [articolo]
Brussino A.; Vaula G.; Cagnoli C.; Panza E.; Seri M.; Di Gregorio E.; Scappaticci S.; Camanini S.; Daniele D.; Bradac G.B.; Pinessi L.; Cavalieri S.; Grosso E.; Migone N.; Brusco A., A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations., «EUROPEAN JOURNAL OF NEUROLOGY», 2010, 17, pp. 541 - 549 [articolo]
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]
Savoia A.; De Rocco D.; Panza E.; Bozzi V.; Scandellari R.; Loffredo G.; Mumford A.; Heller P.G.; Noris P.; De Groot M.R.; Giani M.; Freddi P.; Scognamiglio F.; Riondino S.; Pujol-Moix N.; Fabris F.; Seri M.; Balduini C.L.; Pecci A., Heavy chain myosin 9-related disease (MYH9 -RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder., «THROMBOSIS AND HAEMOSTASIS», 2010, 103, pp. 826 - 832 [articolo]
Pecci A.; Panza E.; De Rocco D.; Pujol-Moix N.; Girotto G.; Podda L.; Paparo C.; Bozzi V.; Pastore A.; Balduini CL.; Seri M.; Savoia A., MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype., «EUROPEAN JOURNAL OF HAEMATOLOGY», 2010, 84, pp. 291 - 297 [articolo]
Graziano C; Carone S; Panza E; Marino F; Magini P; Romeo G; Pession A; Seri M., Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation., «BLOOD», 2009, 114, pp. 1655 - 1657 [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]
Pecci A; Panza E; Pujol-Moix N; Klersy C; Di Bari F; Bozzi V; Gresele P; Lethagen S; Fabris F; Dufour C; Granata A; Doubek M; Pecoraro C; Koivisto PA; Heller PG; Iolascon A; Alvisi P; Schwabe D; De Candia E; Rocca B; Russo U; Ramenghi U; Noris P; Seri M; Balduini CL; Savoia A., Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease., «HUMAN MUTATION», 2008, 29(3), pp. 409 - 417 [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]
Panza E; Marini M; Pecci A; Giacopelli F; Bozzi V; Seri M; Balduini C; Ravazzolo R., Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell lines., «PATHOGENETICS», 2008, 1(1), pp. 1 - 5 [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]
L. Longo; E. Panza; F. Schena; M. Seri; M. Devoto; G. Romeo; C. Bini; G. Pappalardo; G.P. Tonini; P. Perri., Genetic Predisposition to Familial Neuroblastoma: Identification of Two Novel Genomic Regions at 2p and 12p., «HUMAN HEREDITY», 2007, 63(3-4), pp. 205 - 211 [articolo]
