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  • A. Ferrarese Lupi, Annick Rossi, +7 authors Antonella Forlino
  • Biology, Medicine
  • Journal of medical genetics
  • 6 July 2006
  • Prolidase deficiency (PD) is a rare autosomal recessive connective tissue disorder caused by mutations in the prolidase gene. The PD patients show a wide range of clinical outcomes characterisedContinue Reading
  • Antonella Forlino, Chiara Tani, +8 authors Joan C. Marini
  • Biology, Medicine
  • Proteomics
  • 1 June 2007
  • This study used proteomic and transcriptomic techniques to understand the molecular basis of the phenotypic variability in the bone disorder osteogenesis imperfecta (OI). Calvarial bone mRNAContinue Reading
  • Antonella Forlino, A. Ferrarese Lupi, +4 authors Giuseppe Cetta
  • Biology, Medicine
  • Human Genetics
  • 1 October 2002
  • Abstract. Prolidase, a ubiquitously distributed dipeptidase, is involved in the latter stage of degradation of endogenous and dietary proteins and is particularly important in collagen catabolism. ItContinue Reading
  • A. Ferrarese Lupi, Antonio de Riso, +5 authors Antonella Forlino
  • Biology, Medicine
  • Journal of Human Genetics
  • 1 September 2004
  • AbstractProlidase deficiency (PD) is a rare autosomal recessive disorder characterized mainly by skin lesions of the legs and feet, mental retardation, and respiratory infections. Mutations at theContinue Reading