[PDF] Top 20 Hemoglobin sickle cell disease in Brazil
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Hemoglobin sickle cell disease in Brazil
... In our clinic, we have 94 children (median age 3 years, range 1-17 years) and 29 adults (median age 35 years, range 19-81 years) with HbSC disease. It is important to point out that 67% of the patients were ... See full document
1
Risk factors for alloimmunization by patients with sickle cell disease
... recorded in medical charts, including those before ad- mission, from information given by the pa- tient or relative, and from the Blood Center form for transfusion ...unreliable in 208 cases ...available ... See full document
8
Mobile applications for sickle cell disease management: an integrative review
... with sickle cell dis- ...scarce in view of the high in- cidence of sickle cell disease ...cations in Brazil is very ...with sickle cell ... See full document
9
Brazilian Guidelines for transcranial doppler in children and adolescents with sickle cell disease
... cm/s in one or both of the middle cerebral arteries or the distal segment of the internal carotid artery in two exams at an interval of at least two ...stroke in the 63 children in the ... See full document
6
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 ...the disease, there are still several steps of its pathogenesis which are ...be in- volved ... See full document
5
Renal dysfunction in patients with sickle cell anemia or sickle cell trait
... with sickle cell anemia (Hb SS) or sickle cell trait (Hb AS) may present several types of renal dysfunction; however, comparison of the prevalence of these abnormalities between these two ... See full document
6
Rev. Bras. Hematol. Hemoter. vol.37 número6
... Sickle cell disease (SCD) is a monogenic disease that causes a significant reduction in life expectancy due to the presence of chronic anemia, acute painful episodes and organic ...lung ... See full document
2
Osteoporosis and Vitamin D Deficiency in Patients with Sickle Cell Disease
... and hemoglobin levels were the major role players for abnormal BMD in this study ...[5]. In another study on 17 SCA patients, osteopenia frequency was 47% and serum iron and ferritin levels were ... See full document
5
Rev. Bras. Hematol. Hemoter. vol.33 número4
... with sickle cell disease is considered to be the responsibility of blood ...to sickle cell disease children in primary healthcare services will enable the identification ... See full document
6
CHARACTERIZATION OF CASES OF SICKLE CELL DISEASE IN A MICROREGION IN THE PIAUI
... of sickle cell anemia from a micro region in the state of Piauí, emphasizing the treatment adopted during the disease and the vaccination status of the investigated ...with sickle ... See full document
9
Rev. Saúde Pública vol.40 número4
... survival in homozygous sickle-cell disease will become available from patient groups such as the Jamaican Cohort Study, in which patients are iden- tified at birth and prospectively ... See full document
3
Rev. Bras. Hematol. Hemoter. vol.34 número4
... Sickle cell disease (SCD) is an inherited disorder of hemoglobin ...mutation in the β-globin ...of sickle hemoglobin, a protein that has the unique property of ... See full document
1
Fatores de risco para aloimunização em pacientes com anemia falciforme
... practice in the treatment and prevention of complications in sickle cell anemia ...low in the microcirculation by decreasing the percentage of hemoglobin S (HbS) and increasing ... See full document
6
J. Pediatr. (Rio J.) vol.84 número4 suppl. en v84n4s0a12
... recessive disease) has been a problem in neonatal screening since the introduc- tion of tests for sickle cell anemia and cystic ...ers in neonatal ... See full document
11
Sickle cell disease and associated problems: Case study of Homozygous sicklers
... studying in class-3 rd in Government School of the village Deogaon. In general, he doesn’t give normal ...normal in first look except short statures of ...out in the district hospital ... See full document
16
Comparison of oxidative stress and the frequency of polymorphisms in the HFE gene between hemoglobin S trait blood donors and sickle cell disease patients
... The hemoglobin proiles were conirmed using: hemoglobin electrophoresis in alka- line pH cellulose acetate; acidic pH electrophoresis; and high-performance liquid chromatog- raphy (HPLC) ... See full document
9
Self-care of men with priapism and sickle cell disease
... with sickle cell disease and priapism and describe self-care measures in light of Orem’s Self-Care ...of sickle cell disease and ...culty in social interaction and ... See full document
7
S -Haplotypes in sickle cell anemia
... sickle cell disease patients from Salvador, a city in Northeastern Brazil characterized by a population with a large African contribu- tion ...15.9% in different population ... See full document
6
Elevated pulse pressure is associated with hemolysis, proteinuria and chronic kidney disease in sickle cell disease.
... Hemolysis in SCD causes endothelial dysfunction via multiple mechanisms, and both hemolysis and endothelial dysfunction may be independently linked to elevated pulse ...free hemoglobin from hemolyzed RBC ... See full document
14
Remembering the forgotten non-communicable diseases
... than sickle cell disease (SCD) [4]: despite the fact that, with early detec- tion and an inexpensive package of basic care, the ma- jority of those born with the condition can expect to lead a good ... See full document
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