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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: cianci p. 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
Omphalocele in a patient with Noonan syndrome.
Longoni L, D'Apolito V, Cianci P, Selicorni A. Longoni L, et al. Among authors: cianci p. Clin Dysmorphol. 2012 Oct;21(4):215-217. doi: 10.1097/MCD.0b013e3283590a5a. Clin Dysmorphol. 2012. PMID: 22932443 No abstract available.
Collagenopathy with a phenotype resembling Silver-Russell syndrome phenotype.
Cianci P, Paterlini G, Tagliabue P, Verderio M, Vergani P, Bianchi ML, Giussani C, Kullmann G, Mazzoleni F, Bozzetti A, Selicorni A. Cianci P, et al. Am J Med Genet A. 2013 Oct;161A(10):2681-4. doi: 10.1002/ajmg.a.36093. Epub 2013 Aug 5. Am J Med Genet A. 2013. PMID: 23918677 No abstract available.
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis.
Flex E, Jaiswal M, Pantaleoni F, Martinelli S, Strullu M, Fansa EK, Caye A, De Luca A, Lepri F, Dvorsky R, Pannone L, Paolacci S, Zhang SC, Fodale V, Bocchinfuso G, Rossi C, Burkitt-Wright EM, Farrotti A, Stellacci E, Cecchetti S, Ferese R, Bottero L, Castro S, Fenneteau O, Brethon B, Sanchez M, Roberts AE, Yntema HG, Van Der Burgt I, Cianci P, Bondeson ML, Cristina Digilio M, Zampino G, Kerr B, Aoki Y, Loh ML, Palleschi A, Di Schiavi E, Carè A, Selicorni A, Dallapiccola B, Cirstea IC, Stella L, Zenker M, Gelb BD, Cavé H, Ahmadian MR, Tartaglia M. Flex E, et al. Among authors: cianci p. Hum Mol Genet. 2014 Aug 15;23(16):4315-27. doi: 10.1093/hmg/ddu148. Epub 2014 Apr 4. Hum Mol Genet. 2014. PMID: 24705357 Free PMC article.
Hemostatic abnormalities in Noonan syndrome.
Artoni A, Selicorni A, Passamonti SM, Lecchi A, Bucciarelli P, Cerutti M, Cianci P, Gianniello F, Martinelli I. Artoni A, et al. Among authors: cianci p. Pediatrics. 2014 May;133(5):e1299-304. doi: 10.1542/peds.2013-3251. Pediatrics. 2014. PMID: 24753526
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: cianci p. Mol Cytogenet. 2016 Aug 5;9:60. doi: 10.1186/s13039-016-0265-5. eCollection 2016. Mol Cytogenet. 2016. PMID: 27499811 Free PMC article.
130 results