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Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|September 15, 2017
Phototherapy for vitiligo, what's new?Andrea Paro Vidolin, Caterina Aurizi, Giovanni Leone
Molecular Genetics and Metabolism|January 2, 2007
Heterogeneity of mutations in the ferrochelatase gene in Italian patients with erythropoietic protoporphyriaCaterina Aurizi, Xiaoye Schneider-Yin, Fiammetta Sorge, et al.
The EMBO Journal|August 13, 2003
Crystal structure and functional analysis of Escherichia coli glutamate decarboxylaseGuido Capitani, Daniela De Biase, Caterina Aurizi, et al.
Endocrine|March 9, 2018
Novel mutation of PPOX gene in a patient with abdominal pain and syndrome of inappropriate antidiuresisIsabella Tabaro, Giuseppe Reimondo, Giangiacomo Osella, et al.
Journal of Inherited Metabolic Disease|February 11, 2017
Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severityJasmin Barman-Aksoezen, Domenico Girelli, Caterina Aurizi, et al.
Cancers|November 27, 2021
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?Laura Eibenschutz, Silvia Caputo, Emanuela Camera, et al.
Blood Cells, Molecules & Diseases|May 16, 2015
Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genesFrancesca Clementina Radio, Silvia Majore, Caterina Aurizi, et al.
European Journal of Dermatology : EJD|October 6, 2020
Clinical and molecular epidemiology of erythropoietic protoporphyria in ItalyPaolo Ventura, Valentina Brancaleoni, Elena Di Pierro, et al.
European Journal of Human Genetics : EJHG|March 26, 2015
Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in ItalyMartina Nemethova, Jan Radvanszky, Ludevit Kadasi, et al.
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