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E. Di Pierro

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

24

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Metabolic reprogramming and mitochondrial dysfunction in HepG2 cells as potential drivers of AIP pathophysiology

2021 Digestive and Liver Disease
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Anemia and iron metabolism in patients with sars-cov-2 infection: The role of inflammation and hypoxia

2021
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The alternative complement pathway is activated in protoporphyria patients during sun exposure

2020 medRxiv
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Epidemiology of porphyrias in Italy: rare complex diseases with liver involvement- data from the registry of Gruppo Italiano Porfiria (GrIP)

2019 Digestive and Liver Disease
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Transcranial color Doppler in stroke-free adult patients with sickle cell disease

2017 Annals of Hematology
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Laboratory diagnosis of thalassemia

2016 International Journal of Laboratory Hematology
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A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia trait.

2012 British Journal of Dermatology
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Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy.

2009 Cellular and Molecular Biology
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C-terminal deletion in the ALAS2 gene and X-linked dominant protoporphyria

2009
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Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate.

2009 Human Genetics
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