Francesca Granata

A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene

E. Peverelli, P. Cavarzere, R. Gaudino, 2022, Orphanet Journal of Rare Diseases.

Associated Effect of SLC40A1 and TMPRSS6 Polymorphisms on Iron Overload

E. Di Pierro, G. Graziadei, L. Duca, 2022, Metabolites.

The alternative complement pathway is activated in protoporphyria patients during sun exposure.

S. Fustinoni, G. de Luca, E. Di Pierro, 2020, medRxiv.

Quality-Adjusted Life Years in Erythropoietic Protoporphyria and Other Rare Diseases: A Patient-Initiated EQ-5D Feasibility Study

A. Minder, J. Barman-Aksözen, Francesca Granata, 2023, International journal of environmental research and public health.

A puzzling mutation in congenital erythropoietic porphyria and an association with β‐thalassaemia trait

M. Cappellini, S. Itani, Francesca Granata, 2012, The British journal of dermatology.

Dersimelagon in Erythropoietic Protoporphyrias.

Francesca Granata, R. Falchetto, Cornelia Dechant, 2023, The New England journal of medicine.

Fair Funding Decisions: Consistency of the Time Horizons Used in the Calculation of Quality-Adjusted Life Years for Therapies for Very Rare Diseases by the National Institute for Health and Care Excellence in England

J. Barman-Aksözen, Francesca Granata, R. Falchetto, 2024, International journal of environmental research and public health.