Found: 13
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Pulmonary manifestations in young Gaucher disease patients: Phenotype‐genotype correlation and radiological findings.
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- Pediatric Pulmonology, 2020, v. 55, n. 2, p. 441, doi. 10.1002/ppul.24544
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- Article
Immunological role of CD4<sup>+</sup>CD28<sup>null</sup> T lymphocytes, natural killer cells, and interferon-gamma in pediatric patients with sickle cell disease: relation to disease severity and response to therapy.
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- Immunologic Research, 2018, v. 66, n. 4, p. 480, doi. 10.1007/s12026-018-9010-y
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- Article
Urinary Kidney Injury Molecule 1 and Urinary Monocyte Chemotactic Protein 1 as Novelbiomarkers for Early Detection of Sickle Cell Nephropathy.
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- QJM: An International Journal of Medicine, 2024, v. 117, p. i210, doi. 10.1093/qjmed/hcae070.488
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- Article
Role of vitamin C as an adjuvant therapy to different iron chelators in young β-thalassemia major patients: efficacy and safety in relation to tissue iron overload.
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- European Journal of Haematology, 2016, v. 96, n. 3, p. 318, doi. 10.1111/ejh.12594
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- Article
BIRC6/Apollon gene expression in childhood acute leukemia: impact on therapeutic response and prognosis.
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- European Journal of Haematology, 2012, v. 88, n. 2, p. 118, doi. 10.1111/j.1600-0609.2011.01734.x
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- Article
Endothelial nitric oxide synthase gene intron 4 VNTR polymorphism in sickle cell disease: Relation to vasculopathy and disease severity.
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- Pediatric Blood & Cancer, 2015, v. 62, n. 3, p. 389, doi. 10.1002/pbc.25234
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- Article
Ganglion Cell Complex Thinning in Young Gaucher Patients: Relation to Prodromal Parkinsonian Markers.
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- Movement Disorders, 2020, v. 35, n. 12, p. 2211, doi. 10.1002/mds.28256
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- Article
Predictors and risk factors of chronic pulmonary disease in pediatric sickle cell disease.
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- Journal of Applied Hematology, 2019, v. 10, p. S36
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- Article
Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patients.
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- Neurogenetics, 2020, v. 21, n. 3, p. 159, doi. 10.1007/s10048-020-00607-4
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- Article
Soluble fms-Like Tyrosine Kinase 1 as a Link Between Angiogenesis and Endothelial Dysfunction in Pediatric Patients With β-Thalassemia Intermedia.
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- Clinical & Applied Thrombosis/Hemostasis, 2017, v. 23, n. 8, p. 943, doi. 10.1177/1076029617692879
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- Article
Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction.
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- Clinical & Applied Thrombosis/Hemostasis, 2017, v. 23, n. 8, p. 1010, doi. 10.1177/1076029616665921
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- Article
Tartrate-Resistant Acid Phosphatase 5b in Young Patients With Sickle Cell Disease and Trait Siblings.
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- Clinical & Applied Thrombosis/Hemostasis, 2017, v. 23, n. 1, p. 64, doi. 10.1177/1076029615594001
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- Article
Vascular Dysfunction in Patients With Young β-Thalassemia.
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- Clinical & Applied Thrombosis/Hemostasis, 2015, v. 21, n. 8, p. 733, doi. 10.1177/1076029614541515
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- Article