Paolo Moi
Cagliari, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 24 publications
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome.
Journal: Clinical genetics
Published: March 04, 2025
Reduced cyclin D3 expression in erythroid cells protects against malaria.
Journal: Nature
Published: February 21, 2024
miR-365-3p mediates BCL11A and SOX6 erythroid-specific coregulation: A new player in HbF activation.
miR-365-3p mediates BCL11A and SOX6 erythroid-specific coregulation: A new player in HbF activation.
Journal: Molecular therapy. Nucleic acids
Published: December 15, 2022
A New Intronic Variant in ECEL1 in Two Patients with Distal Arthrogryposis Type 5D.
Journal: International journal of molecular sciences
Published: December 03, 2020
Induction of therapeutic levels of HbF in genome-edited primary β0 39-thalassaemia haematopoietic stem and progenitor cells.
Journal: British journal of haematology
Published: May 12, 2020
The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene.
Journal: Haematologica
Published: October 30, 2019
Quality of life in Sardinian patients with transfusion-dependent Thalassemia: a cross-sectional study.
Journal: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation
Published: June 05, 2018
Hematological phenotypes in children according to the α-globin genotypes.
Journal: Blood cells, molecules & diseases
Published: October 07, 2017
Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment.
Journal: American journal of hematology
Published: August 20, 2017
Earlier initiation of transfusional and iron chelation therapies in recently born children with transfusion-dependent thalassemia.
Journal: American journal of hematology
Published: June 13, 2017
Last Updated: 09/26/2026