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Haematologica|August 1, 2020
Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in CyprusPetros Kountouris, Kyriaki Michailidou, Soteroula Christou, et al.Hemoglobin|April 18, 2009
Hemoglobin variants in CyprusAndreani R Kyrri, Xenia Felekis, Eleni Kalogerou, et al.Biomedicines|February 24, 2024
Unravelling the Complexity of the +33 C>G [HBB:c.-18C>G] Variant in Beta ThalassemiaCoralea Stephanou, Miranda Petrou, Petros Kountouris, et al.Human Mutation|May 23, 2019
A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β-thalassemia majorPavlos Fanis, Ioanna Kousiappa, Marios Phylactides, et al.International Journal of Molecular Sciences|September 16, 2020
Relative and Absolute Quantification of Aberrant and Normal Splice Variants in HBB β-ThalassemiaPetros Patsali, Panayiota Papasavva, Soteroulla Christou, et al.Pediatric Endocrinology Reviews : PER|February 8, 2006
The impact of iron overload and genotype on gonadal function in women with thalassaemia majorNicos Skordis, Maritsa Gourni, Constantinos Kanaris, et al.International Journal of Molecular Sciences|February 15, 2022
CRISPR Editing Enables Consequential Tag-Activated MicroRNA-Mediated Endogene DeactivationPanayiota L Papasavva, Petros Patsali, Constantinos C Loucari, et al.Journal of Blood Medicine|March 5, 2015
Recent trends in the gene therapy of β-thalassemiaAlessia Finotti, Laura Breda, Carsten W Lederer, et al.European Journal of Haematology|June 28, 2006
The impact of genotype on endocrine complications in thalassaemia majorNicos Skordis, Monica Michaelidou, Savvas C Savva, et al.International Journal of Molecular Sciences|December 23, 2022
A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with HaemoglobinopathiesAnna Minaidou, Stella Tamana, Coralea Stephanou, et al.Pageof 8