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Sickle Cell Health Awareness, Perspectives, and Experiences (SHAPE) survey: Perspectives of adolescent and adult patients, caregivers, and healthcare professionals on the burden of sickle cell disease.
- Published in:
- European Journal of Haematology, 2024, v. 113, n. 2, p. 172, doi. 10.1111/ejh.14211
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- Article
BMP6 and VDR gene polymorphisms are associated with osteonecrosis in a sickle cell anaemia cohort.
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- British Journal of Haematology, 2024, v. 204, n. 4, p. 1507, doi. 10.1111/bjh.19329
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- Article
Piezo1 activation augments sickling propensity and the adhesive properties of sickle red blood cells in a calcium‐dependent manner.
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- British Journal of Haematology, 2023, v. 202, n. 3, p. 657, doi. 10.1111/bjh.18799
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- Article
Hematologic Malignancies Patients Face High Symptom Burden and Are Lately Referred to Palliative Consultation: Analysis of a Single Center Experience.
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- American Journal of Hospice & Palliative Medicine, 2023, v. 40, n. 7, p. 761, doi. 10.1177/10499091221132285
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- Article
Role of Macrophages in Sickle Cell Disease Erythrophagocytosis and Erythropoiesis.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6333, doi. 10.3390/ijms24076333
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- Article
Safe use of hydroxycarbamide in sickle cell disease patients hospitalized for painful vaso‐occlusive episodes during the randomized, open‐label HELPS study.
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- British Journal of Haematology, 2022, v. 199, n. 1, p. 153, doi. 10.1111/bjh.18349
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- Article
Economic burden of sickle cell disease in Brazil.
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- PLoS ONE, 2022, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0269703
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- Article
Accelerated low‐density neutrophil transition in sickle cell anaemia may contribute to disease pathophysiology.
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- British Journal of Haematology, 2022, v. 197, n. 2, p. 232, doi. 10.1111/bjh.18009
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- Article
Up‐regulation of miR‐130a is related to leg ulcers in sickle cell anaemia.
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- British Journal of Haematology, 2022, v. 197, n. 1, p. e16, doi. 10.1111/bjh.18018
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- Article
Reduced blood pressure in sickle cell disease is associated with decreased angiotensin converting enzyme (ACE) activity and is not modulated by ACE inhibition.
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- PLoS ONE, 2022, v. 17, n. 2, p. 1, doi. 10.1371/journal.pone.0263424
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- Article
Association of genetic variants rs641153 (CFB), rs2230199 (C3), and rs1410996 (CFH) with age-related macular degeneration in a Brazilian population.
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- Experimental Biology & Medicine, 2021, v. 246, n. 21, p. 2290, doi. 10.1177/15353702211024543
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- Article
Heme induces significant neutrophil adhesion in vitro via an NFκB and reactive oxygen species-dependent pathway.
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- Molecular & Cellular Biochemistry, 2021, v. 476, n. 11, p. 3963, doi. 10.1007/s11010-021-04210-5
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- Article
Association of KLOTHO polymorphisms with clinical complications of sickle cell anemia.
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- Annals of Hematology, 2021, v. 100, n. 8, p. 1921, doi. 10.1007/s00277-021-04532-w
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- Article
Diagnostic Accuracy of HemotypeSC as a Point-of-Care Testing Device for Sickle Cell Disease: Findings from a Southwestern State in Nigeria and Implications for Patient Care in Resource-Poor Settings of sub-Saharan Africa.
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- Global Pediatric Health, 2021, p. 1, doi. 10.1177/2333794X211016789
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- Article
Evaluation of APOE polymorphisms and the risk for age-related macular degeneration in a Southeastern Brazilian population.
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- Experimental Biology & Medicine, 2021, v. 246, n. 10, p. 1148, doi. 10.1177/1535370220985466
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- Publication type:
- Article
Influence of UGT1A1 promoter polymorphism, α-thalassemia and βs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
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- Annals of Hematology, 2021, v. 100, n. 4, p. 903, doi. 10.1007/s00277-021-04422-1
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- Publication type:
- Article
Diagnostic Accuracy of HemotypeSC as a Point-of-Care Testing Device for Sickle Cell Disease: Findings from a Southwestern State in Nigeria and Implications for Patient Care in Resource-Poor Settings of sub-Saharan Africa.
- Published in:
- Global Pediatric Health, 2021, p. 1, doi. 10.1177/2333794X211016789
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- Publication type:
- Article
CXCR4<sup>hi</sup> effector neutrophils in sickle cell anemia: potential role for elevated circulating serotonin (5-HT) in CXCR4<sup>hi</sup> neutrophil polarization.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71078-8
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- Article
High levels of proinflammatory cytokines IL-6 and IL-8 are associated with a poor clinical outcome in sickle cell anemia.
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- 2020
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- journal article
Angiogenesis-Related Genes in Endothelial Progenitor Cells May Be Involved in Sickle Cell Stroke.
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- 2020
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- Publication type:
- journal article
Association between ANXA2*5681 polymorphism (rs7170178) and osteonecrosis in haemoglobin SS‐genotyped patients.
- Published in:
- British Journal of Haematology, 2020, v. 188, n. 3, p. e8, doi. 10.1111/bjh.16267
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- Article
Longitudinal sequencing of RUNX1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignancies.
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- British Journal of Haematology, 2019, v. 186, n. 5, p. 724, doi. 10.1111/bjh.15990
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- Article
Global gene expression reveals an increase of HMGB1 and APEX1 proteins and their involvement in oxidative stress, apoptosis and inflammation pathways among beta‐thalassaemia intermedia and major phenotypes.
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- British Journal of Haematology, 2019, v. 186, n. 4, p. 608, doi. 10.1111/bjh.16062
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- Article
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47313-2
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- Article
S100A8 acts as an autocrine priming signal for heme‐induced human Mϕ pro‐inflammatory responses in hemolytic inflammation.
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- Journal of Leukocyte Biology, 2019, v. 106, n. 1, p. 35, doi. 10.1002/JLB.3MIA1118-418RR
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- Article
Highlight Article: Different morphological and gene expression profile in placentas of the same sickle cell anemia patient in pregnancies of opposite outcomes.
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- Experimental Biology & Medicine, 2019, v. 244, n. 5, p. 395, doi. 10.1177/1535370219834305
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- Article
Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia.
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- 2019
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- journal article
Recombinant erythropoietin as alternative to red cell transfusion in sickle cell disease.
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- Vox Sanguinis, 2019, v. 114, n. 2, p. 178, doi. 10.1111/vox.12750
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- Article
Global analysis of erythroid cells redox status reveals the involvement of Prdx1 and Prdx2 in the severity of beta thalassemia.
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- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208316
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- Article
Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child.
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- 2018
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- journal article
Interleukin‐6 G‐174C polymorphism predicts higher risk of stroke in sickle cell anaemia.
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- British Journal of Haematology, 2018, v. 182, n. 2, p. 294, doi. 10.1111/bjh.14773
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- Article
Deferasirox associated with liver failure and death in a sickle cell anemia patient homozygous for the −1774delG polymorphism in the Abcc2 gene.
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- Clinical Case Reports, 2017, v. 5, n. 8, p. 1218, doi. 10.1002/ccr3.1040
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- Article
Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
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- Experimental Biology & Medicine, 2017, v. 242, n. 3, p. 267, doi. 10.1177/1535370216668052
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- Article
Sympathetic Hyperactivity, Increased Tyrosine Hydroxylase and Exaggerated Corpus Cavernosum Relaxations Associated with Oxidative Stress Plays a Major Role in the Penis Dysfunction in Townes Sickle Cell Mouse.
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- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0166291
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- Article
Abnormal expression of inflammatory genes in placentas of women with sickle cell anemia and sickle hemoglobin C disease.
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- 2016
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- Publication type:
- journal article
Expanding the Knowledge on Lignocellulolytic and Redox Enzymes of Worker and Soldier Castes from the Lower Termite Coptotermes gestroi.
- Published in:
- Frontiers in Microbiology, 2016, v. 7, p. 1, doi. 10.3389/fmicb.2016.01518
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- Article
Clinically relevant RHD-CE genotypes in patients with sickle cell disease and in African Brazilian donors.
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- Blood Transfusion (17232007), 2016, v. 14, n. 5, p. 449, doi. 10.2450/2016.0275-15
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- Article
Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci.
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- British Journal of Haematology, 2016, v. 173, n. 3, p. 456, doi. 10.1111/bjh.13961
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- Publication type:
- Article
Association of Nitric Oxide Synthase and Matrix Metalloprotease Single Nucleotide Polymorphisms with Preeclampsia and Its Complications.
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- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0136693
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- Publication type:
- Article
Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminus.
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- Journal of Clinical Investigation, 2015, v. 125, n. 3, p. 993, doi. 10.1172/JCI75714
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- Publication type:
- Article
Influence of the [beta](s) haplotype and [alpha]-thalassemia on stroke development in a Brazilian population with sickle cell anaemia.
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- 2014
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- Publication type:
- Journal Article
Brain perfusion impairment in neurologically asymptomatic adult patients with sickle-cell disease shown by voxel-based analysis of SPECT images.
- Published in:
- Frontiers in Neurology, 2013, v. 4, p. 1, doi. 10.3389/fneur.2013.00207
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- Article
Hydroxyurea reduces leukocyte interactions with the vessel wall in a haemolytic mouse model via a possible NO/cGMP-mediated effect.
- Published in:
- 2013
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- Abstract
Viability of umbilical cord blood mononuclear cell subsets until 96 hours after collection.
- Published in:
- Transfusion, 2013, v. 53, n. 9, p. 2034, doi. 10.1111/trf.12078
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- Article
Identification of genes located at breakpoints of uncharacterized chromosomal translocations by the use of chromosomal microdissection and next generation DNA sequencing.
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- BMC Proceedings, 2013, v. 7, n. Suppl 2, p. 1, doi. 10.1186/1753-6561-7-S2-P55
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- Publication type:
- Article
Elevated plasma levels and platelet-associated expression of the pro-thrombotic and pro-inflammatory protein, TNFSF14 (LIGHT), in sickle cell disease.
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- British Journal of Haematology, 2012, v. 158, n. 6, p. 788, doi. 10.1111/j.1365-2141.2012.09218.x
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- Article
Thalassemia major phenotypes secondary to the association of β 5′ UTR +20( C→ T) allele with β 39( C→ T).
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- European Journal of Haematology, 2012, v. 89, n. 3, p. 273, doi. 10.1111/j.1600-0609.2012.01813.x
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- Article
Molecular characteristics and chromatin texture features in acute promyelocytic leukemia.
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- Diagnostic Pathology, 2012, v. 7, n. 1, p. 75, doi. 10.1186/1746-1596-7-75
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- Article
Inhibition of phosphodiesterase 9A reduces cytokine-stimulated in vitro adhesion of neutrophils from sickle cell anemia individuals.
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- Inflammation Research, 2011, v. 60, n. 7, p. 633, doi. 10.1007/s00011-011-0315-8
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- Publication type:
- Article
Increased adhesive properties of platelets in sickle cell disease: roles for α<sub>IIb</sub>β<sub>3</sub>-mediated ligand binding, diminished cAMP signalling and increased phosphodiesterase 3A activity.
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- British Journal of Haematology, 2010, v. 149, n. 2, p. 280, doi. 10.1111/j.1365-2141.2010.08087.x
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- Article