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Minerva Medica|October 13, 1983
[The association between liver cirrhosis and bacterial endocarditis. Description of a typical case]F Zolezzi, G Capella, E TraversiMolecular and Cellular Probes|June 1, 1996
Intrafamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 geneL Cohen-Solal, F Zolezzi, P F Pignatti, et al.Giornale Italiano Di Cardiologia|July 1, 1983
[Complete sub-His AV block caused by carotid sinus massage. Possible direct vagal effect on the His-Purkinje system]G Capella, F Zolezzi, M Azzini, et al.Human Mutation|January 8, 2000
Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. OnlineM Mottes, M Gomez Lira, F Zolezzi, et al.Giornale Italiano Di Cardiologia|March 1, 1986
Chronic myocarditis leading to a right ventricular cardiomyopathy. Case reportF Zolezzi, E Filippi, R Rosso, et al.Human Heredity|February 25, 2000
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of italian families with Marfan syndromeM Mottes, S Mirandola, F Rigatelli, et al.American Journal of Medical Genetics|August 22, 1997
Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variabilityF Zolezzi, M Valli, M Clementi, et al.European Journal of Biochemistry|October 1, 1993
Gly85 to Val substitution in pro alpha 1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestionM Valli, F Zolezzi, M Mottes, et al.Human Molecular Genetics|December 1, 1994
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helixA Forlino, F Zolezzi, M Valli, et al.Pageof 2