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Arquivos brasileiros de cardiologia, ISSN 0066-782X, 01/2017, Volume 109, Issue 3 Supl 1, pp. 1 - 104
Journal Article
British journal of haematology, ISSN 0007-1048, 11/2015, Volume 171, Issue 4, pp. 631 - 637
haemolytic anaemia | clinical studies | haemoglobinopathies | erythrocytes | sickle cell disease | Sickle cell disease | Clinical studies | Haemolytic anaemia | Haemoglobinopathies | Erythrocytes | Life Sciences & Biomedicine | Hematology | Science & Technology | Hemoglobin SC Disease - complications | Follow-Up Studies | Hemoglobin SC Disease - blood | Humans | Middle Aged | Male | Hemoglobin SC Disease - mortality | Young Adult | Retinal Diseases - etiology | Aged, 80 and over | Pain - etiology | Adult | Female | Child | Hearing Loss, Sensorineural - mortality | Brazil - epidemiology | Osteonecrosis - etiology | Comorbidity | Kaplan-Meier Estimate | Proportional Hazards Models | Cholelithiasis - etiology | Delayed Diagnosis | Hemoglobin SC Disease - diagnosis | Pregnancy | Hearing Loss, Sensorineural - etiology | Adolescent | Aged | Pregnancy Complications, Hematologic - epidemiology | Medicine, Experimental | Hemoglobin | Medical research | Sickle cell anemia | Patient outcomes | Mortality | Index Medicus
Journal Article
Transfusion (Philadelphia, Pa.), ISSN 0041-1132, 07/2018, Volume 58, Issue 7, pp. 1578 - 1579
Journal Article
British journal of haematology, ISSN 0007-1048, 06/2019, Volume 185, Issue 5, pp. 918 - 924
Toll‐like receptor | immunogenetics | rs4696480 | bacterial infections | sickle cell disease | Toll-like receptor | Life Sciences & Biomedicine | Hematology | Science & Technology | Care and treatment | Disease susceptibility | Sickle cell anemia | Single nucleotide polymorphisms | Health aspects | Immunization | Immune response | Bacterial infections | Prophylaxis | Inflammatory response | Infections | Single-nucleotide polymorphism | Morbidity | Hyposplenism | Confidence intervals | Genetic variance | Genotype & phenotype | TLR2 protein | Penicillin | Toll-like receptors | Bacteria | Genetic factors | Sickle cell disease | Age composition | Index Medicus
Journal Article
Blood cells, molecules, & diseases, ISSN 1079-9796, 06/2017, Volume 65, pp. 8 - 15
Life Sciences & Biomedicine | Hematology | Science & Technology | Reproducibility of Results | Humans | Genotype | Genetic Testing - methods | Genetic Variation | Isoantibodies - blood | Anemia, Sickle Cell - therapy | Phenotype | Rh-Hr Blood-Group System - genetics | Alleles | Isoantibodies - immunology | Disease Management | High-Throughput Nucleotide Sequencing | Anemia, Sickle Cell - blood | Anemia, Sickle Cell - diagnosis | Anemia, Sickle Cell - genetics | Blood Transfusion - methods | Sickle cell anemia | Viral antibodies | Antibodies | Genetic aspects | Analysis | Index Medicus
Journal Article
American journal of hematology, ISSN 0361-8609, 04/2012, Volume 87, Issue 4, pp. 439 - 442
Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Polycythemias | Biological and medical sciences | Medical sciences | Diseases of red blood cells | Polycythemia - genetics | Humans | Middle Aged | Molecular Sequence Data | Male | Mutation, Missense | Procollagen-Proline Dioxygenase - metabolism | Basic Helix-Loop-Helix Transcription Factors - metabolism | Base Sequence | Conserved Sequence | Adult | Female | Von Hippel-Lindau Tumor Suppressor Protein - metabolism | Amino Acid Sequence | Basic Helix-Loop-Helix Transcription Factors - genetics | Exons - genetics | Hypoxia-Inducible Factor-Proline Dioxygenases | Signal Transduction - genetics | Erythropoietin - physiology | Polycythemia - congenital | Protein Interaction Mapping | Sequence Homology, Amino Acid | Point Mutation | Sequence Alignment | Heterozygote | Amino Acid Substitution | Basic Helix-Loop-Helix Transcription Factors - chemistry | erythrocytosis | Hypoxia Inducible Factor-2α | oxygen-sensing | erythropoietin | prolyl hydroxylation
Journal Article
Transfusion medicine (Oxford, England), ISSN 0958-7578, 12/2020, Volume 30, Issue 6, pp. 522 - 524
Journal Article
The New England journal of medicine, ISSN 0028-4793, 02/2017, Volume 376, Issue 5, pp. 429 - 439
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | P-Selectin - antagonists & inhibitors | Double-Blind Method | Pain - prevention & control | Anemia, Sickle Cell - complications | Antibodies, Monoclonal - pharmacology | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Antibodies, Monoclonal - therapeutic use | Male | Anemia, Sickle Cell - drug therapy | Young Adult | Adolescent | Pain - etiology | Quality of Life | Adult | Female | Hydroxyurea - therapeutic use | Drug Therapy, Combination | P-Selectin - immunology | Viral antibodies | Prevention | Usage | Care and treatment | Safety and security measures | Sickle cell anemia | Antibodies | Dosage and administration | Patients | Occlusion | Spleen | Chest | Arthralgia | Body weight | Neutrophils | Diarrhea | Hydroxyurea | Inflammation | Pruritus | Cell interactions | Endothelial cells | Endothelium | Pain | Blood platelets | Vomiting | Transgenic animals | Hemoglobin | Sickle cell disease | P-selectin | Index Medicus | Abridged Index Medicus
Journal Article
Frontiers in immunology, ISSN 1664-3224, 09/2020, Volume 11, pp. 2041 - 2041
inflammation markers | non-classical HLA | sickle cell complications | sickle cell retinopathy | toll-like receptor (TLR) | NK cell receptors and ligands | CTLA 4 | sickle cell disease | Life Sciences & Biomedicine | Immunology | Science & Technology | Complications and side effects | Care and treatment | Genetic aspects | Sickle cell anemia | Genes | Genetic polymorphisms | Index Medicus
Journal Article
Arquivos brasileiros de cardiologia, ISSN 0066-782X, 09/2017, Volume 109, Issue 3, pp. 1 - 104
Journal Article