L. De Falco

发表

Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice

D. Sinclair, A. Iolascon, M. Cappellini, 2014, Haematologica.

β-spectrinBari: a truncated β-chain responsible for dominant hereditary spherocytosis

S. Perrotta, A. Iolascon, F. Della Ragione, 2009, Haematologica.

The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease

D. Girelli, A. Iolascon, L. De Falco, 2018, American journal of hematology.

Novel TMPRSS6 mutations associated with iron‐refractory iron deficiency anemia (IRIDA)

D. Girelli, A. Iolascon, L. De Falco, 2010, Human mutation.

Performance of cell-free DNA sequencing-based non-invasive prenatal testing: experience on 36,456 singleton and multiple pregnancies

L. De Falco, A. Torella, M. Torella, 2021, BMC medical genomics.

Peroxiredoxin-2: A Novel Regulator of Iron Homeostasis in Ineffective Erythropoiesis.

T. Ganz, D. Melisi, S. Mueller, 2018, Antioxidants & redox signaling.

Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency.

M. Fleming, K. Finberg, A. Iolascon, 2018, Blood.

Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?

A. Iolascon, L. De Falco, U. Koçak, 2013, The Turkish journal of pediatrics.

MED12 Mutation in Two Families with X-Linked Ohdo Syndrome

L. De Falco, A. Sensi, Antonio Fico, 2021, Genes.

Human skin-derived keratinocytes and fibroblasts co-cultured on 3D poly ε-caprolactone scaffold support in vitro HSC differentiation into T-lineage committed cells.

C. Pignata, V. Guarino, L. Ambrosio, 2013, International immunology.

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis

A. Pantaleo, A. Iolascon, L. De Franceschi, 2009, Haematologica.

How I Diagnose Non-thalassemic Microcytic Anemias.

Achille Iolascon, A. Iolascon, L. De Falco, 2015, Seminars in hematology.

Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis

A. Iolascon, M. Cappellini, L. De Franceschi, 2011, Haematologica.

Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells

M. Gorrese, A. Iolascon, R. Russo, 2010, Haematologica.

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

Ivan Limongelli, Gordon W Stewart, Achille Iolascon, 2013, Blood.

Iron refractory iron deficiency anemia

M. Muckenthaler, C. Beaumont, A. Iolascon, 2013, Haematologica.

Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis

C. Beaumont, A. Iolascon, L. De Falco, 2009, Haematologica.

The role of Matriptase-2 during the early postnatal development in humans

D. Girelli, A. Iolascon, L. De Falco, 2016, Haematologica.

The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload.

A. Iolascon, L. De Falco, L. Silvestri, 2007, Blood.

Iron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutations

L. De Falco, E. Keskin, Luigia De Falco, 2016, Pediatric hematology and oncology.

Fyn kinase is a novel modulator of erythropoietin signaling and stress erythropoiesis

A. Iolascon, L. De Franceschi, L. De Falco, 2018, American journal of hematology.

Fyn is Involved in Erythropoietin Signaling Pathway and Interfaces Oxidation to Regulate Erythropoiesis

A. Iolascon, L. De Franceschi, L. De Falco, 2018, bioRxiv.

The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in b-Thalassemic Erythropoiesis

A. Iolascon, Soo‐Young Choi, L. De Franceschi, 2015 .

Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II.

D. Girelli, A. Iolascon, R. Russo, 2016, Blood.

Mutations in the gene encoding DMT1: clinical presentation and treatment.

A. Iolascon, L. De Falco, 2009, Seminars in hematology.

Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings

A. Iolascon, L. De Falco, E. Marciano, 2017, American journal of medical genetics. Part A.

A Case Report of a Feto-Placental Mosaicism Involving a Segmental Aneuploidy: A Challenge for Genome Wide Screening by Non-Invasive Prenatal Testing of Cell-Free DNA in Maternal Plasma

A. Di Spiezio Sardo, L. De Falco, Antonio Fico, 2023, Genes.

Detection of SRY‐positive46,XX male syndrome by the analysis of cell‐free fetal DNA via non‐invasive prenatal testing

L. De Falco, Antonio Fico, Raffaella Ruggiero, 2019, Clinical case reports.

Non-Invasive Prenatal Screening: The First Report of Pentasomy X Detected by Plasma Cell-Free DNA and Karyotype Analysis

L. De Falco, Antonio Fico, Raffaella Ruggiero, 2022, Diagnostics.

Congenital dyserythropoietic anaemias: new acquisitions.

A. Iolascon, R. Russo, L. De Falco, 2011, Blood transfusion = Trasfusione del sangue.

Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia.

A. Iolascon, L. De Falco, P. Vajro, 2007, Haematologica.

Detection of 46, XY Disorder of Sex Development (DSD) Based on Plasma Cell-Free DNA and Targeted Next-Generation Sequencing

L. De Falco, Antonio Fico, C. Piscopo, 2021, Genes.

The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis.

L. De Franceschi, L. De Falco, X. An, 2015, Antioxidants & redox signaling.

Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis

A. Iolascon, M. Cappellini, L. De Franceschi, 2011, Haematologica.

Iron refractory iron deficiency anemia

M. Muckenthaler, C. Beaumont, A. Iolascon, 2013, Haematologica.