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Williams-Beuren Syndrome and celiac disease: A real association?
Pangallo E, Parma B, Mariani M, Cianci P, De Paoli A, Maitz S, Fossati C, Panceri R, Agosti M, Selicorni A. Pangallo E, et al. Among authors: fossati c. Eur J Med Genet. 2020 Sep;63(9):103999. doi: 10.1016/j.ejmg.2020.103999. Epub 2020 Jul 2. Eur J Med Genet. 2020. PMID: 32622956
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases.
Cianci P, D'Apolito V, Moretti A, Barbagallo M, Paci S, Carbone MT, Lubrano R, Urbino A, Dionisi Vici C, Memo L, Zampino G, La Marca G, Villani A, Corsello G, Selicorni A; Italian Society of Pediatrics (SIP); Italian Society of Pediatric Genetic Diseases and Congenital Disabilities (SIMGePed) the Italian Society of Pediatric Emergency Medicine (SIMEUP); Italian Society For The Study Of Inborn Metabolic Disorders And Newborn Screening (SIMMENS) and Members of Italian Network. Cianci P, et al. Ital J Pediatr. 2020 Nov 23;46(1):173. doi: 10.1186/s13052-020-00937-x. Ital J Pediatr. 2020. PMID: 33228805 Free PMC article.
14q32.3-qter trisomic segment: a case report and literature review.
Villa N, Scatigno A, Redaelli S, Conconi D, Cianci P, Farina C, Fossati C, Dalprà L, Maitz S, Selicorni A. Villa N, et al. Among authors: fossati c. Mol Cytogenet. 2016 Aug 5;9:60. doi: 10.1186/s13039-016-0265-5. eCollection 2016. Mol Cytogenet. 2016. PMID: 27499811 Free PMC article.
Sleep disorders in Cornelia de Lange syndrome.
Zambrelli E, Fossati C, Turner K, Taiana M, Vignoli A, Gervasini C, Russo S, Furia F, Masciadri M, Ajmone P, Kullman G, Canevini MP, Selicorni A. Zambrelli E, et al. Among authors: fossati c. Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):214-21. doi: 10.1002/ajmg.c.31497. Epub 2016 May 2. Am J Med Genet C Semin Med Genet. 2016. PMID: 27133889
457 results