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Bulla R, De Seta F, Radillo O, Agostinis C, Durigutto P, Pellis V, De Santo D, Crovella S, Tedesco F. Mannose-binding lectin is produced by vaginal epithelial cells and its level in the vaginal fluid is influenced by progesterone. Mol Immunol 2010;48(1-3):281-6.
Byrne S, Jansen L, U-King-Im J-M, Siddiqui A, Lidov HGW, Bodi I, Smith L, Mein R, Cullup T, Dionisi-Vici C, Al-Gazali L, Al-Owain M, Bruwer Z, Thihli KAl, El-Garhy R, Flanigan KM, Manickam K, Zmuda E, Banks W, Gershoni-Baruch R, Mandel H, Dagan E, Raas-Rothschild A, Barash H, Filloux F, Creel D, Harris M, Hamosh A, Kölker S, Ebrahimi-Fakhari D, Hoffmann GF, Manchester D, Boyer PJ, Manzur AY, Lourenco CMarques, Pilz DT, Kamath A, Prabhakar P, Rao VK, R Rogers C, Ryan MM, Brown NJ, McLean CA, Said E, Schara U, Stein A, Sewry C, Travan L, Wijburg FA, Zenker M, Mohammed S, Fanto M, Gautel M, Jungbluth H. EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy. Brain 2016;139(Pt 3):765-81.
C
Calatroni M, Oliva E, Gianfreda D, Gregorini G, Allinovi M, Ramirez GA, Bozzolo EP, Monti S, Bracaglia C, Marucci G, Bodria M, Sinico RA, Pieruzzi F, Moroni G, Pastore S, Emmi G, Esposito P, Catanoso M, Barbano G, Bonanni A, Vaglio A. ANCA-associated vasculitis in childhood: recent advances. Ital J Pediatr 2017;43(1):46.
Calitri C, Gabiano C, Galli L, Chiappini E, Giaquinto C, Buffolano W, Genovese O, Esposito S, Bernardi S, de Martino M, Tovo P-A. The second generation of HIV-1 vertically exposed infants: a case series from the Italian Register for paediatric HIV infection. BMC Infect Dis 2014;14:277.
Callea F, Callea M. Adam's rib and the origin of stem cells. Am J Hematol 2011;86(6):529.
Callea M, Bellacchio E, Fattori F, Bertini E, Callea F, Cammarata-Scalisi F. Acute myeloid leukemia in a 3 years old child with cleidocranial dysplasia. Leuk Lymphoma 2015;:1-3.
Callea M, Vinciguerra A, Willoughby CE, Deroma L, Clarich G. Infantile bilateral glaucoma in a child with ectodermal dysplasia. Ophthalmic Genet 2013;34(1-2):58-60.
Callea M, Yavuz I, Clarich G, Cammarata-Scalisi F. [Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2015;113(6):e341-4.
Callea M, Cammarata-Scalisi F, Willoughby CE, Giglio SR, Sani I, Bargiacchi S, Traficante G, Bellacchio E, Tadini G, Yavuz I, Galeotti A, Clarich G. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2017;115(1):e34-e38.
Callea M, Willoughby CE, Nieminen P, Di Stazio M, Bellacchio E, Giglio S, Sani I, Vinciguerra A, Maglione M, Tadini G, Clarich G. Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia. J Eur Acad Dermatol Venereol 2015;29(5):1032-4.
Calligaris L, Berti I, Barbi E. Phleboliths as a marker of slow-flow venous malformation. Arch Dis Child 2015;100(11):1012.
Calligaris L, Marzuillo P, Barbi E. Re: Tramadol can selectively manage moderate pain in children following European advice limiting codeine use. Acta Paediatr 2014;103(11):e466.

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