Found: 39
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M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05360-2
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- Publication type:
- Article
Safety, Pharmacokinetics, and Pharmacodynamics of Etavopivat (FT‐4202), an Allosteric Activator of Pyruvate Kinase‐R, in Healthy Adults: A Randomized, Placebo‐Controlled, Double‐Blind, First‐in‐Human Phase 1 Trial.
- Published in:
- Clinical Pharmacology in Drug Development, 2022, v. 11, n. 5, p. 654, doi. 10.1002/cpdd.1058
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- Publication type:
- Article
Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia.
- Published in:
- Frontiers in Physiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphys.2021.636609
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- Publication type:
- Article
Autoimmune Hemolytic Anemia in the Pediatric Setting.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 2, p. 216, doi. 10.3390/jcm10020216
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- Publication type:
- Article
Phylogenetic and Ontogenetic View of Erythroblastic Islands.
- Published in:
- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/873628
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- Publication type:
- Article
A pharmacokinetic–pharmacodynamic analysis of l‐glutamine for the treatment of sickle cell disease: Implications for understanding the mechanism of action and evaluating response to therapy.
- Published in:
- British Journal of Haematology, 2024, v. 205, n. 3, p. 1147, doi. 10.1111/bjh.19632
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- Publication type:
- Article
Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics‐guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia.
- Published in:
- British Journal of Haematology, 2021, v. 194, n. 3, p. 617, doi. 10.1111/bjh.17663
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- Publication type:
- Article
Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease.
- Published in:
- British Journal of Haematology, 2020, v. 190, n. 4, p. 599, doi. 10.1111/bjh.16671
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- Publication type:
- Article
Congenital dyserythropoietic anaemia type I diagnosed in a young adult with a history of splenectomy in childhood for presumed haemolytic anaemia.
- Published in:
- British Journal of Haematology, 2018, v. 182, n. 1, p. 10, doi. 10.1111/bjh.15217
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- Publication type:
- Article
Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab.
- Published in:
- British Journal of Haematology, 2016, v. 175, n. 4, p. 744, doi. 10.1111/bjh.13884
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- Publication type:
- Article
Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial.
- Published in:
- British Journal of Haematology, 2016, v. 172, n. 1, p. 122, doi. 10.1111/bjh.13791
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- Publication type:
- Article
Hemolytic anemia and macrothrombocytopenia: A lipid problem?
- Published in:
- American Journal of Hematology, 2023, v. 98, n. 8, p. 1335, doi. 10.1002/ajh.26916
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- Publication type:
- Article
Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis.
- Published in:
- American Journal of Hematology, 2022, v. 97, n. 10, p. 1384, doi. 10.1002/ajh.26662
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- Publication type:
- Article
Human TLR8 induces inflammatory bone marrow erythromyeloblastic islands and anemia in SLE-prone mice.
- Published in:
- Life Science Alliance, 2023, v. 6, n. 10, p. 1, doi. 10.26508/lsa.202302241
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- Publication type:
- Article
Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening.
- Published in:
- FASEB Journal, 2022, v. 36, n. 6, p. 1, doi. 10.1096/fj.202100809RR
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- Article
ER-to-Golgi transport and SEC23-dependent COPII vesicles regulate T cell alloimmunity.
- Published in:
- 2021
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- Publication type:
- journal article
Pathogenesis of ELANE-mutant severe neutropenia revealed by induced pluripotent stem cells.
- Published in:
- Journal of Clinical Investigation, 2015, v. 125, n. 8, p. 3103, doi. 10.1172/JCI80924
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- Publication type:
- Article
Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-86582-8
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- Publication type:
- Article
Unraveling Macrophage Heterogeneity in Erythroblastic Islands.
- Published in:
- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01140
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- Publication type:
- Article
Pediatric myelofibrosis due to compound heterozygous MPIG6B mutations in a patient of European ancestry.
- Published in:
- Pediatric Blood & Cancer, 2023, v. 70, n. 3, p. 1, doi. 10.1002/pbc.30023
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- Publication type:
- Article
Implementation of near-universal hydroxyurea uptake among children with sickle cell anemia: A single-center experience.
- Published in:
- 2021
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- Publication type:
- journal article
How I approach hereditary hemolytic anemia and splenectomy.
- Published in:
- 2020
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- Publication type:
- journal article
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity.
- Published in:
- 2019
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- Publication type:
- journal article
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.
- Published in:
- American Journal of Hematology, 2019, v. 94, n. 8, p. 871, doi. 10.1002/ajh.25510
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- Publication type:
- Article
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.
- Published in:
- American Journal of Hematology, 2019, v. 94, n. 1, p. 149, doi. 10.1002/ajh.25325
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- Publication type:
- Article
Hereditary xerocytosis: Diagnostic considerations.
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 3, p. E67, doi. 10.1002/ajh.24996
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- Publication type:
- Article
Effects of hydroxyurea treatment for patients with hemoglobin SC disease.
- Published in:
- American Journal of Hematology, 2016, v. 91, n. 2, p. 238, doi. 10.1002/ajh.24255
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- Publication type:
- Article
Clinical outcomes of splenectomy in children: Report of the splenectomy in congenital hemolytic anemia registry.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 3, p. 187, doi. 10.1002/ajh.23888
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- Publication type:
- Article
Immunosuppressive CD71<sup>+</sup> erythroid cells compromise neonatal host defence against infection.
- Published in:
- Nature, 2013, v. 504, n. 7478, p. 158, doi. 10.1038/nature12675
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- Publication type:
- Article
A Population Pharmacokinetic Analysis of l-Glutamine Exposure in Patients with Sickle Cell Disease: Evaluation of Dose and Food Effects.
- Published in:
- Clinical Pharmacokinetics, 2024, v. 63, n. 3, p. 357, doi. 10.1007/s40262-024-01349-4
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- Publication type:
- Article
Corrigendum: The Spectrum of SPTA1 -Associated Hereditary Spherocytosis.
- Published in:
- 2019
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- Publication type:
- Correction Notice
The Spectrum of SPTA1 -Associated Hereditary Spherocytosis.
- Published in:
- Frontiers in Physiology, 2019, p. 1, doi. 10.3389/fphys.2019.00815
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- Publication type:
- Article
Compound heterozygosity for two novel mutations in the erythrocyte protein 4.2 gene causing spherocytosis in a Caucasian patient.
- Published in:
- British Journal of Haematology, 2011, v. 152, n. 6, p. 780, doi. 10.1111/j.1365-2141.2010.08516.x
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- Publication type:
- Article
The impact of the 2009 H1N1 influenza pandemic on pediatric patients with sickle cell disease.
- Published in:
- Pediatric Blood & Cancer, 2011, v. 57, n. 4, p. 648, doi. 10.1002/pbc.23030
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- Publication type:
- Article
Cooperating G6PD mutations associated with severe neonatal hyperbilirubinemia and cholestasis.
- Published in:
- Pediatric Blood & Cancer, 2011, v. 56, n. 5, p. 840, doi. 10.1002/pbc.22744
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- Publication type:
- Article
Pelger-Huët anomaly in a child with 1q42.3-44 deletion.
- Published in:
- Pediatric Blood & Cancer, 2006, v. 46, n. 5, p. 645, doi. 10.1002/pbc.20504
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- Publication type:
- Article
Targeting erythroblast-specific apoptosis in experimental anemia.
- Published in:
- Apoptosis, 2008, v. 13, n. 8, p. 1022, doi. 10.1007/s10495-008-0236-3
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- Article
Alu element insertion in <italic>PKLR</italic> gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients.
- Published in:
- Human Mutation, 2018, v. 39, n. 3, p. 389, doi. 10.1002/humu.23392
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- Publication type:
- Article
A painless erythematous swelling of the external ear as a manifestation of Lyme disease: a case report.
- Published in:
- 2020
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- Publication type:
- journal article