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Orphanet Journal of Rare Diseases|November 1, 2006
Congenital pulmonary lymphangiectasiaCarlo Bellini, Francesco Boccardo, Corradino Campisi, et al.Clinical Chemistry and Laboratory Medicine|November 1, 2007
Reliability assessment of glucose measurement by HemoCue analyser in a neonatal intensive care unitCarlo Bellini, Giovanni Serra, Domenico Risso, et al.Microsurgery|January 29, 2008
Pediatric lymphedema and correlated syndromes: role of microsurgeryCorradino Campisi, Elisa Da Rin, Carlo Bellini, et al.Microsurgery|March 18, 2010
Microsurgery for lymphedema: clinical research and long-term resultsCorradino Campisi, Carlo Bellini, Corrado Campisi, et al.American Journal of Medical Genetics. Part A|February 28, 2006
Nonimmune idiopathic hydrops fetalis and congenital lymphatic dysplasiaCarlo Bellini, Raoul C M Hennekam, Francesco Boccardo, et al.The Journal of Pediatrics|March 19, 2008
Lymphatic dysplasias in newborns and children: the role of lymphoscintigraphyCarlo Bellini, Francesco Boccardo, Corradino Campisi, et al.American Journal of Medical Genetics. Part A|December 4, 2004
Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasiaEugenio Bonioli, Raoul C Hennekam, Gianantonio Spena, et al.American Journal of Medical Genetics. Part A|April 1, 2009
Etiology of nonimmune hydrops fetalis: a systematic reviewCarlo Bellini, Raoul C M Hennekam, Ezio Fulcheri, et al.Neurogenetics|August 9, 2005
X-linked creatine transporter deficiency: clinical description of a patient with a novel SLC6A8 gene mutationMaria C Schiaffino, Carlo Bellini, Laura Costabello, et al.Journal of Vascular Surgery|June 13, 2006
Diagnosis and management of primary chylous ascitesCorradino Campisi, Carlo Bellini, Costantino Eretta, et al.Pageof 2