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Comparative analysis of oral and intravenous iron therapy in rat models of  inflammatory anemia and iron deficiency | Haematologica
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica

Hypercoagulability and thrombotic complications in hemolytic anemias |  Haematologica
Hypercoagulability and thrombotic complications in hemolytic anemias | Haematologica

Logistic‐Nomogram model based on red blood cell parameters to differentiate  thalassemia trait and iron deficiency anemia in southern region of Fujian  Province, China - Xu - 2023 - Journal of Clinical Laboratory
Logistic‐Nomogram model based on red blood cell parameters to differentiate thalassemia trait and iron deficiency anemia in southern region of Fujian Province, China - Xu - 2023 - Journal of Clinical Laboratory

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical  phenotype in Fanconi anemia | Haematologica
Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia | Haematologica

Genotype-phenotype and outcome associations in patients with Fanconi anemia:  the National Cancer Institute cohort | Haematologica
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica

PDF) Molecular analysis of Fanconi anemia: the experience of the Bone  Marrow Failure Study Group of the Italian Association of Pediatric  Onco-Hematology | U. Ramenghi - Academia.edu
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology | U. Ramenghi - Academia.edu

PDF) Mosaic segmental uniparental isodisomy and progressive clonal  selection: A common mechanism of late onset β-thalassemia major
PDF) Mosaic segmental uniparental isodisomy and progressive clonal selection: A common mechanism of late onset β-thalassemia major

Molecular basis of inherited microcytic anemia due to defects in iron  acquisition or heme synthesis. - Abstract - Europe PMC
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. - Abstract - Europe PMC

Vol. 106 No. 5 (2021): May, 2021 | Haematologica
Vol. 106 No. 5 (2021): May, 2021 | Haematologica

Comparative analysis of oral and intravenous iron therapy in rat models of  inflammatory anemia and iron deficiency | Haematologica
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica

PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3  and ameliorates anemia in beta-thalassemic mice
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice

Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Haematologica, Volume 105, issue 2 by Haematologica - Issuu

PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary  hypertension in patients with hemoglobinopathies
PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies

Haematologica, Volume 101, issue 2 by Haematologica - Issuu
Haematologica, Volume 101, issue 2 by Haematologica - Issuu

Circulating microparticles in children with sickle cell anemia: a  heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin  | Haematologica
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica

Haematologica, Volume 106, Issue 11 by Haematologica - Issuu
Haematologica, Volume 106, Issue 11 by Haematologica - Issuu

Molecular basis of inherited microcytic anemia due to defects in iron  acquisition or heme synthesis. - Abstract - Europe PMC
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. - Abstract - Europe PMC

Congenital sideroblastic anemia associated with germline polymorphisms  reducing expression of FECH | Haematologica
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica

Haematologica, Volume 104, Issue 3 by Haematologica - Issuu
Haematologica, Volume 104, Issue 3 by Haematologica - Issuu

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity  and transfusion dependency | Haematologica
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica

Pathogenic mutations identified by a multimodality approach in 117 Japanese  Fanconi anemia patients | Haematologica
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients | Haematologica

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

Haematologica, Volume 106, Issue 9 by Haematologica - Issuu
Haematologica, Volume 106, Issue 9 by Haematologica - Issuu