F. C. Radio

A novel missense mutation in SLC40A1 results in resistance to hepcidin and confirms the existence of two ferroportin‐associated iron overload diseases

C. Férec, P. Grammatico, E. Létocart, 2009, British journal of haematology.

Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major

M. Testi, M. Andreani, M. Troiano, 2009, Haematologica.

Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.

F. Torricelli, P. Grammatico, D. Giannarelli, 2015, Blood cells, molecules & diseases.

The controversial role of variants in HAMP , BMP 2 , FTL and SLC 40 A 1 genes

F. Torricelli, P. Grammatico, D. Giannarelli, 2015 .

TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy.

P. Grammatico, S. Majore, F. C. Radio, 2014, Blood cells, molecules & diseases.

Natural history of TFR2‐related hereditary hemochromatosis in a 47‐yr‐old Italian patient

M. Castori, P. Grammatico, S. Majore, 2009, European journal of haematology.

The “old theme” of variability versus transitory phenotypes in thanatophoric dysplasia type 1: Two 19‐week‐old fetuses with (“San Diego” variant) and without ragged metaphyses due to the same FGFR3 mutation

M. Castori, S. Morlino, P. Grammatico, 2013, American journal of medical genetics. Part A.

A novel germline mutation in CDK4 codon 24 associated to familial melanoma

I. Bottillo, A. Paiardini, S. Bargiacchi, 2018, Clinical genetics.