Browsing by Subject Thalassemia -- Malta
Showing results 1 to 11 of 11
| Issue Date | Title | Author(s) |
| 2022 | Analysis of the foetal to adult globin gene switch mechanism by single cell RNA and TCR sequencing | Mangion, Sharon (2022) |
| 1998 | Clinical and molecular pathology of the β+ IVSI-6C thalassaemia in Malta | Scerri, Christian A. |
| 2022 | Differential expression of globin gene switching using single cell sequencing | Buttigieg, Michaela (2022) |
| 2013 | Does summation of HMIP SNPs differentiate between the Hb F of the β°Codon39 and the β+IVS-I-6C thalassaemia heterozygotes? | Eljali, Seham Saadeddin |
| 2012 | The effect of modifier genes on foetal Haemoglobin in the Maltese population | Scerri, Gary |
| 2012 | KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients | Borg, Joseph J.; Phylactides, Marios; Bartsakoulia, Marina; Tafrali, Christina; Lederer, Carsten W.; Felice, Alex; Papachatzopoulou, Adamantia; Kourakli, Alexandra; Stavrou, Eleana F.; Christou, Soteroula; Hou, Jun; Karkabouna, Sophia; Lappa-Manakou, Christina; Ozgur, Zeliha; Ijcken, Wilfred van; Lindern, Marieke von; Grosveld, Frank G.; Georgitsi, Marianthi; Kleanthous, Marina; Philipsen, Sjaak; Patrinos, George P. |
| 2012 | Pharmacogenomic reactivation of foetal haemoglobin | Grech, Laura |
| 2022 | Quantitative mRNA expression profiling of primary human erythroid progenitor cells exposed to small molecules for HbF induction | Borg, Elena (2022) |
| 1966 | The Thalassemia trait in Malta and Gozo | Vella, Francis |
| 2020 | To relate clinical phenotype to genotype and underlying inflammation among a cohort of thalassaemia homozygotes | Cutajar, Michaela |
| 2023 | Unravelling the globin gene switch mechanism in patients with hereditary persistence of foetal haemoglobin | Camilleri, Nikita (2023) |
