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Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophyVITELLI, F; VILLANOVA, M; MALANDRINI, A et al.Muscle & nerve. 1999, Vol 22, Num 10, pp 1437-1441, issn 0148-639XArticle

Microsatellite instability in sporadic mucinous colorectal carcinomas : Relationship to clinico-pathological variablesMESSERINI, L; VITELLI, F; DE VITIS, L. R et al.Journal of pathology. 1997, Vol 182, Num 4, pp 380-384, issn 0022-3417Article

Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomasPAPI, L; DE VITIS, L. R; VITELLI, F et al.Human genetics. 1995, Vol 95, Num 3, pp 347-351, issn 0340-6717Article

Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)VITELLI, F; PICCINI, M; CAROLI, F et al.Genomics (San Diego, Calif.). 1999, Vol 55, Num 3, pp 335-340, issn 0888-7543Article

KCNE1-like gene is deleted in AMME contiguous gene syndrome : Identification and characterization of the human and mouse homologsPICCINI, M; VITELLI, F; SERI, M et al.Genomics (San Diego, Calif.). 1999, Vol 60, Num 3, pp 251-257, issn 0888-7543Article

Relation of fibre intake to HbA_1c and the prevalence of severe ketoacidosis and severe hypoglycaemiaBUYKEN, A. E; TOELLER, M; HEITKAMP, G et al.Diabetologia (Berlin). 1998, Vol 41, Num 8, pp 882-890, issn 0012-186XArticle

Changes in plasma growth hormone in diabetic and nondiabetic subjects during the glucose clampSHARP, P. S; VISWANATHAN MOHAN; MANESCHI, F et al.Metabolism, clinical and experimental. 1987, Vol 36, Num 1, pp 71-75, issn 0026-0495Article

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FACL4, a new gene encoding long-chain Acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationPICCINI, M; VITELLI, F; BRUTTINI, M et al.Genomics (San Diego, Calif.). 1998, Vol 47, Num 3, pp 350-358, issn 0888-7543Article