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Evaluation of two in vitro assays for tumorigenicity assessment of  CRISPR-Cas9 genome-edited cells: Molecular Therapy - Methods & Clinical  Development
Evaluation of two in vitro assays for tumorigenicity assessment of CRISPR-Cas9 genome-edited cells: Molecular Therapy - Methods & Clinical Development

Haematologica, Volume 106, Issue 5 by Haematologica - Issuu
Haematologica, Volume 106, Issue 5 by Haematologica - Issuu

IJMS | Free Full-Text | Iron Overload and Chelation Therapy in  Non-Transfusion Dependent Thalassemia
IJMS | Free Full-Text | Iron Overload and Chelation Therapy in Non-Transfusion Dependent Thalassemia

Inflammation and myeloid malignancy: quenching the flame - ScienceDirect
Inflammation and myeloid malignancy: quenching the flame - ScienceDirect

Cancers | Free Full-Text | Impact of Immune Parameters and Immune  Dysfunctions on the Prognosis of Patients with Chronic Lymphocytic Leukemia
Cancers | Free Full-Text | Impact of Immune Parameters and Immune Dysfunctions on the Prognosis of Patients with Chronic Lymphocytic Leukemia

Haematologica, Volume 102, issue 12 by Haematologica - Issuu
Haematologica, Volume 102, issue 12 by Haematologica - Issuu

PDF) Tailoring iron chelation by iron intake and serum ferritin: The  prospective EPIC study of deferasirox in 1744 patients with  transfusion-dependent anemias
PDF) Tailoring iron chelation by iron intake and serum ferritin: The prospective EPIC study of deferasirox in 1744 patients with transfusion-dependent anemias

Haematologica, Volume 102, issue 10 by Haematologica - Issuu
Haematologica, Volume 102, issue 10 by Haematologica - Issuu

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Risk factors and outcomes according to age at transplantation with an  HLA-identical sibling for sickle cell disease | Haematologica
Risk factors and outcomes according to age at transplantation with an HLA-identical sibling for sickle cell disease | Haematologica

Clinical risks and healthcare utilization of hematopoietic cell  transplantation for sickle cell disease in the USA using merged
Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged

Cureus | Blood Demand and Challenges for Patients With Beta-Thalassemia  Major in Eastern Saudi Arabia | Article
Cureus | Blood Demand and Challenges for Patients With Beta-Thalassemia Major in Eastern Saudi Arabia | Article

PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and  clinical phenotype in Fanconi anemia
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia

Haematologica, Volume 106, Issue 2 by Haematologica - Issuu
Haematologica, Volume 106, Issue 2 by Haematologica - Issuu

IJMS | Free Full-Text | Genetic Biomarkers and Their Clinical Implications  in B-Cell Acute Lymphoblastic Leukemia in Children
IJMS | Free Full-Text | Genetic Biomarkers and Their Clinical Implications in B-Cell Acute Lymphoblastic Leukemia in Children

Clinical risks and healthcare utilization of hematopoietic cell  transplantation for sickle cell disease in the USA using merged
Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged

Vol. 102 No. 6 (2017): June, 2017 | Haematologica
Vol. 102 No. 6 (2017): June, 2017 | Haematologica

Biomedicines | Free Full-Text | Measurable Residual Disease and Clonal  Evolution in Acute Myeloid Leukemia from Diagnosis to Post-Transplant  Follow-Up: The Role of Next-Generation Sequencing
Biomedicines | Free Full-Text | Measurable Residual Disease and Clonal Evolution in Acute Myeloid Leukemia from Diagnosis to Post-Transplant Follow-Up: The Role of Next-Generation Sequencing

Haematologica, Volume 107, Issue 7 by Haematologica - Issuu
Haematologica, Volume 107, Issue 7 by Haematologica - Issuu

PDF) The many faces of IKZF1 in B-cell precursor acute lymphoblastic  leukemia
PDF) The many faces of IKZF1 in B-cell precursor acute lymphoblastic leukemia

High‐level induction of fetal haemoglobin by pomalidomide in  β‐thalassaemia/HbE erythroid progenitor cells - Khamphikham - 2020 -  British Journal of Haematology - Wiley Online Library
High‐level induction of fetal haemoglobin by pomalidomide in β‐thalassaemia/HbE erythroid progenitor cells - Khamphikham - 2020 - British Journal of Haematology - Wiley Online Library

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Haematologica, Volume 106, Issue 1 by Haematologica - Issuu
Haematologica, Volume 106, Issue 1 by Haematologica - Issuu

Labile plasma iron levels predict survival in patients with lower-risk  Myelodysplastic syndromes
Labile plasma iron levels predict survival in patients with lower-risk Myelodysplastic syndromes

Haematologica, Volume 102, issue 11 by Haematologica - Issuu
Haematologica, Volume 102, issue 11 by Haematologica - Issuu

Quality of life in patients with β‐thalassemia: A prospective study of  transfusion‐dependent and non‐transfusion‐dependent patients in Greece,  Italy, Lebanon, and Thailand - Cappellini - 2019 - American Journal of  Hematology - Wiley
Quality of life in patients with β‐thalassemia: A prospective study of transfusion‐dependent and non‐transfusion‐dependent patients in Greece, Italy, Lebanon, and Thailand - Cappellini - 2019 - American Journal of Hematology - Wiley