C. Aurizi

发表

Glutathione S-transferase ϴ-subunit as a phenotypic suppressor of pmr1Δ strain, the Kluyveromyces lactis model for Hailey-Hailey disease.

S. Cialfi, D. Uccelletti, G. Biolcati, 2016, Biochimica et biophysica acta.

Association between porphyria cutanea tarda and beta-thalassemia major.

G. Biolcati, A. Macrì, L. Barbieri, 2009, Cellular and molecular biology.

Crystal structure and functional analysis of Escherichia coli glutamate decarboxylase

M. Grütter, G. Capitani, F. Bossa, 2003, The EMBO journal.

Phototherapy for vitiligo, what's new?

G. Leone, A. Paro Vidolin, C. Aurizi, 2017, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

Efficacy of the melanocortin analogue Nle4-D-Phe7-α-melanocyte-stimulating hormone in the treatment of patients with Hailey–Hailey disease

I. Screpanti, S. Cialfi, G. Biolcati, 2013, Clinical and experimental dermatology.

Clinical and molecular epidemiology of erythropoietic protoporphyria in Italy

S. Fustinoni, M. Cappellini, E. Di Pierro, 2020, European Journal of Dermatology.

Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on ‘black bone disease’ in Italy

Douglas E. V. Pires, Ludevit Kadasi, Jan Radvanszky, 2015, European Journal of Human Genetics.

Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity

D. Girelli, X. Schneider-Yin, E. Minder, 2017, Journal of Inherited Metabolic Disease.

Novel mutation of PPOX gene in a patient with abdominal pain and syndrome of inappropriate antidiuresis

D. Giachino, G. Reimondo, M. Terzolo, 2018, Endocrine.

Evaluation of Hedgehog Pathway Inhibition on Nevoid Basal Cell Carcinoma Syndrome Fibroblasts and Basal Cell Carcinoma-Associated Fibroblasts: Are Vismodegib and Sonidegib Useful to Target Cancer-Prone Fibroblasts?

E. Camera, C. Cota, L. Eibenschutz, 2021, Cancers.

Heterogeneity of mutations in the ferrochelatase gene in Italian patients with erythropoietic protoporphyria.

X. Schneider-Yin, E. Minder, G. Biolcati, 2007, Molecular genetics and metabolism.

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 .