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[PDF] Top 20 Interleukin 8 as a vaso-occlusive marker in Brazilian patients with sickle cell disease

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Interleukin 8 as a vaso-occlusive marker in Brazilian patients with sickle cell disease

Interleukin 8 as a vaso-occlusive marker in Brazilian patients with sickle cell disease

... Sickle cell disease has a worldwide distribution and is a public health problem in ...Although vaso-occlusive crisis (VOC) is one of the most important clinical features of the ... See full document

5

Rev. Bras. Hematol. Hemoter.  vol.31 número4

Rev. Bras. Hematol. Hemoter. vol.31 número4

... Sickle cell disease is an inflammatory condition with a pathophysiology that involves vaso-occlusive ...vascular disease. Due to the importance of identifying risk factors ... See full document

2

Risk Factors of Pulmonary Hypertension in Brazilian Patients with Sickle Cell Anemia.

Risk Factors of Pulmonary Hypertension in Brazilian Patients with Sickle Cell Anemia.

... [25]. Sickle cell anemia is a hemolytic red cell disorder and all patients with SCD have variable degrees of hemolysis and it is most severe in ...hemolysis in SS varies ... See full document

14

Rev. Bras. Hematol. Hemoter.  vol.36 número5

Rev. Bras. Hematol. Hemoter. vol.36 número5

... Pregnancy in patients with sickle cell disease (SCD) has always been a challenge for both hematologists and ...the sickle vaso-occlusive process has enabled ... See full document

2

Impact of iron oload on interleukin10 levels, biochemical parameters and oxidative stress in patients with sickle cell anemia

Impact of iron oload on interleukin10 levels, biochemical parameters and oxidative stress in patients with sickle cell anemia

... cytokine with potent anti-inlammatory activity which reduces the production of various cytokines including IL-1, IL-6, IL-8, IL-12, TNF-α and GM-CSF to promote uptake and retention of iron in the ... See full document

6

Fatores de risco para aloimunização em pacientes com anemia falciforme

Fatores de risco para aloimunização em pacientes com anemia falciforme

... therapy with packed red blood cells (PRBCs) is a common practice in the treatment and prevention of complications in sickle cell anemia ...of patients with SS receive ... See full document

6

Osteoporosis and Vitamin D  Deficiency in Patients with Sickle Cell Disease

Osteoporosis and Vitamin D Deficiency in Patients with Sickle Cell Disease

... Sickle cell disease (SCD) is one of the most common hemo- globinopathies in the ...Turkey; in some areas such as the Çu- kurova region, this frequency reaches up to ...inlammatory ... See full document

5

Risk factors for alloimmunization by patients with sickle cell disease

Risk factors for alloimmunization by patients with sickle cell disease

... reported in most interna- tional studies (8,11). A Brazilian study (15) reported 20% anti-D antibody among a total of 15 alloantibodies ...found in the present study may be attributed to several ... See full document

8

Rev. Bras. Hematol. Hemoter.  vol.34 número2

Rev. Bras. Hematol. Hemoter. vol.34 número2

... involvement in sickle cell disease has been poorly studied and it is mainly characterized by osteonecrosis, osteomyelitis and ...care in sickle cell disease ... See full document

9

Dilemma in differentiating between acute osteomyelitis and bone infarction in children with sickle cell disease: the role of ultrasound.

Dilemma in differentiating between acute osteomyelitis and bone infarction in children with sickle cell disease: the role of ultrasound.

... Sickle Cell Disease (SCD) is a clinically significant haemoglo- binopathy with increasing incidence in developed ...1 in every 2000 births in England and it is estimated ... See full document

7

Alterações renais nas doenças falciformes.

Alterações renais nas doenças falciformes.

... Sickle cell disease is associated with glomerular and tabular structural abnormalities, hemodynamic changes and renal hormone synthesis alterations (erythropoietin, renin, ...appear in ... See full document

6

Arq. Gastroenterol.  vol.45 número4

Arq. Gastroenterol. vol.45 número4

... – Sickle cell disease causes chronic and recurrent hemolysis which is a recognized risk factor for ...occurs in 50% of adults with sickle cell ...symptomatic ... See full document

6

Renal tubular dysfunction in sickle cell disease

Renal tubular dysfunction in sickle cell disease

... study with 160 children with different renal diseases found a significant association between the inability to concentrate urine and glomerular filtration rate [36], but we did not found this in our ... See full document

10

Analysis of BCL11A gene polymorphisms and hemolysis parameters in patients with sickle-cell disease

Analysis of BCL11A gene polymorphisms and hemolysis parameters in patients with sickle-cell disease

... region, with a significant increase in genotype A/A (mutant) compared to G/G genotype ...associated with the region rs7557939 on the BCL11A gene in SCD adult patients at ...polymorphism ... See full document

6

MANAGEMENT OF SICKLE CELL DISEASE

MANAGEMENT OF SICKLE CELL DISEASE

... The disease is not uniformly seen everywhere but it has some topographical ...distribution. In India, it is frequently seen in Central India, in and around the vicinity of Chhattisgarh ... See full document

4

Partial Red Blood Cell Exchange in Children and Young Patients with Sickle Cell Disease: Manual Versus Automated Procedure

Partial Red Blood Cell Exchange in Children and Young Patients with Sickle Cell Disease: Manual Versus Automated Procedure

... diferences in terms of age and weight between both groups, we did not find that those differences affected the patient ...management. In our cohort, A-RBCX decreased HbS levels more efficiently than manual ... See full document

7

Diagnóstico de hipertensão pulmonar em indivíduos adultos com doença falciforme

Diagnóstico de hipertensão pulmonar em indivíduos adultos com doença falciforme

... com vaso-oclusão, também têm sido ligadas à HP, como a ß-talassemia intermedia, a doença da hemoglobina H, a esferocitose hereditária, a estomatocitose hereditária e a hemoglobinúria paroxística noturna (HPN) ... See full document

153

Guidelines on the treatment of primary immune thrombocytopenia in children and adolescents: Associacao Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associacao Medica Brasileira - 2012

Guidelines on the treatment of primary immune thrombocytopenia in children and adolescents: Associacao Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associacao Medica Brasileira - 2012

... published in 1997 of 149 patients (14 patients under 15 years old), the indications for splenectomy were hematological diseases (27%), trauma (33%), incidental (12%), accidental (20%) and others ... See full document

11

Severe vaso-occlusive retinopathy associated with systemic lupus erythematosus

Severe vaso-occlusive retinopathy associated with systemic lupus erythematosus

... analyses. In immunoserology, elevated titres of antinuclear antibodies and circulating immune complexes were present, while other analyses (anticardiolipin antibodies and lupus anticoagulant) were ...syndrome ... See full document

4

Role of interleukin-3 as a prognostic marker in septic patients

Role of interleukin-3 as a prognostic marker in septic patients

... Patients were assessed for potential inclusion at the time of admission in the ICU or immediately after the diagnosis of sepsis, in case they were already at the ICU. The clinical data were collected ... See full document

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