DI PIERRO, ELENA
DI PIERRO, ELENA
DIPARTIMENTO DI MEDICINA INTERNA (attivo dal 01/01/1998 al 27/04/2012)
The role of hypoxia and inflammation in the regulation of iron metabolism and erythropoiesis in COVID-19: The IRONCOVID study
2022 D. Maira, L. Duca, F. Busti, D. Consonni, M. Salvatici, A. Vianello, A. Milani, A. Guzzardella, E. Di Pierro, S. Aliberti, I.M. Baldini, A. Bandera, F. Blasi, E. Cassinerio, M. Cesari, A.L. Fracanzani, G. Grasselli, G. Graziadei, R. Lombardi, G. Marchi, N. Montano, V. Monzani, F. Peyvandi, M. Proietti, M. Sandri, L. Valenti, M.D. Cappellini, D. Girelli, A. Protti, I. Motta
The α-Lipoic Acid Improves Hepatic Metabolic Dysfunctions in Acute Intermittent Porphyria: A Proof-of-Concept Study
2021 M. Longo, E. Paolini, M. Meroni, L. Duca, I. Motta, A.L. Fracanzani, E. DI PIERRO, P. Dongiovanni
Laboratory diagnosis of porphyria
2021 E. Di Pierro, M. De Canio, R. Mercadante, M. Savino, F. Granata, D. Tavazzi, A.M. Nicolli, A. Trevisan, S. Marchini, S. Fustinoni
$\upalpha$-Lipoic Acid Improves Hepatic Metabolic Dysfunctions in Acute Intermittent Porphyria: A Proof-of-Concept Study [alpha-Lipoic Acid Improves Hepatic Metabolic Dysfunctions in Acute Intermittent Porphyria: A Proof-of-Concept Study]
2021 M. Longo, E. Paolini, M. Meroni, L. Duca, I. Motta, A.L. Fracanzani, E. Di Pierro, P. Dongiovanni
Alternative Pathway Involvement in Protoporphyria Patients Related to Sun Exposure
2021 F. Granata, L. Duca, V. Brancaleoni, S. Fustinoni, G. De Luca, I. Motta, G. Graziadei, E. Di Pierro
Clinical and molecular epidemiology of erythropoietic protoporphyria in Italy
2020 P. Ventura, V. Brancaleoni, E. Di Pierro, G. Graziadei, A. Macrì, C. Carmine Guida, A. Nicolli, M.T. Rossi, F. Granata, V. Fiorentino, S. Fustinoni, R. Sala, P.C. Pinton, A. Trevisan, S. Marchini, C. Cuoghi, M. Marcacci, E. Corradini, F. Sorge, C. Aurizi, M.G. Savino, M.D. Cappellini, A. Pietrangelo
Targeted resequencing of FECH locus reveals that a novel deep intronic pathogenic variant and eQTLs may cause erythropoietic protoporphyria (EPP) through a methylation-dependent mechanism
2019 M. Chiara, I. Primon, L. Tarantini, L. Agnelli, V. Brancaleoni, F. Granata, V. Bollati, E. Di Pierro
Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes
2018 V. Brancaleoni, H.M. Moukhadder, D. Consonni, S. Koussa, E. Di Pierro, M.D. Cappellini, A. Taher
An unusual diagnosis in a 31-year-old man with abdominal pain and hyponatremia
2018 F. Depetri, M. Cugno, G. Graziadei, E. Di Pierro, F. Granata, F. Peyvandi, M.D. Cappellini
Digital PCR (dPCR) analysis reveals that the homozygous c.315–48T>C variant in the FECH gene might cause erythropoietic protoporphyria (EPP)
2018 V. Brancaleoni, F. Granata, P. Missineo, S. Fustinoni, G. Graziadei, E. Di Pierro
Transcranial color Doppler in stroke-free adult patients with sickle cell disease
2017 G. Graziadei, F.M. Casoni, F. Annoni, I. Cortinovis, P. Ridolfi, I. Gandolfi, A. Marcon, E. Di Pierro, M.D. Cappellini
Seven novel genetic mutations within the 5 ' UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria (vol 49, pg 147, 2012)
2016 V. Brancaleoni, F. Granata, A. Colancecco, D. Tavazzi, M.D. Cappellini, E. Di Pierro
Laboratory diagnosis of thalassemia
2016 V. Brancaleoni, E. Di Pierro, I. Motta, M.D. Cappellini
The assessment of noncoding variant of PPOX gene in variegate porphyria reveals post-transcriptional role of the 5′ untranslated exon 1
2016 V. Fiorentino, V. Brancaleoni, F. Granata, G. Graziadei, E. Di Pierro
Molecular basis of β-Thalassemia intermedia in Erbil Province of Iraqi Kurdistan
2015 R.P. Shamoon, N.A.S. Al Allawi, M.D. Cappellini, E. Di Pierro, V. Brancaleoni, F. Granata
Congenital erythropoietic porphyria linked to GATA1-R216W mutation: challenges for diagnosis
2015 E. Di Pierro, R. Russo, Z. Karakas, V. Brancaleoni, A. Gambale, I. Kurt, S.S. Winter, F. Granata, D.R. Czuchlewski, C. Langella, A. Iolascon, M.D. Cappellini
Probes for use in diagnsing Porphyria and allelic quantification of porphyria related genes by ligation and amplification reactions - gene HMBS
2014 E. Di Pierro, M.D. Cappellini, V. Besana, V. Brancaleoni
Seven novel genetic mutations within the 5’utr and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria
2012 F. Granata, V. Brancaleoni, D. Tavazzi, M..D. Cappellini, E. Di Pierro
Does C-terminal deletion in the ALAS2 gene cause x-linked dominant or recessive protoporphyria?
2012 V. Brancaleoni, E. Di Pierro, F. Granata, M.D. Cappellini, E. Di Pierro
Seven novel genetic mutations within the 5′UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria
2012 V. Brancaleoni, F. Granata, A. Colancecco, D. Tavazzi, M.D. Cappellini , E. Di Pierro