Caterina Aurizi

Rome, 00144, Italy

Last Updated: 09/26/2026

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Found 9 publications

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?

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?

Journal: Cancers

Published: October 13, 2021

Clinical and molecular epidemiology of erythropoietic protoporphyria in Italy.

Clinical and molecular epidemiology of erythropoietic protoporphyria in Italy.

Journal: European journal of dermatology : EJD

Published: October 06, 2020

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

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

Journal: Endocrine

Published: December 27, 2017

Phototherapy for vitiligo, what's new?

Phototherapy for vitiligo, what's new?

Journal: Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia

Published: September 15, 2017

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

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

Journal: Journal of inherited metabolic disease

Published: October 12, 2016

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

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

Journal: Biochimica et biophysica acta

Published: April 01, 2016

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

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

Journal: Blood cells, molecules & diseases

Published: February 12, 2015

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

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

Journal: European journal of human genetics : EJHG

Published: October 31, 2014

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

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

Journal: Clinical and experimental dermatology

Published: March 01, 2013

Showing 1-9 of 9

Last Updated: 09/26/2026