[PDF] Top 20 MANAGEMENT OF SICKLE CELL DISEASE
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MANAGEMENT OF SICKLE CELL DISEASE
... The disease is not uniformly seen everywhere but it has some topographical ...vicinity of Chhattisgarh in some religions in caste like kurmis, satnami, mahar, other backward caste and some tribes, it has ... See full document
4
Mobile applications for sickle cell disease management: an integrative review
... results of this review showed that the first mobile applications developed for the management of sickle-cell disease considered symptom recording, such as pain crisis episodes, ... See full document
9
Risk factors for alloimmunization by patients with sickle cell disease
... total of 15 alloantibodies detected. The compara- tively high frequency of anti-D antibodies found in the present study may be attributed to several ...history of the patients was not always ... See full document
8
Braz. J. Oral Sci. vol.12 número3
... manifestations of sickle cell disease on the orofacial complex through a review of current literature concerning prevalence of dental caries, periodontal disease, ... See full document
5
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 ... See full document
19
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
Rev. Bras. Hematol. Hemoter. vol.39 número1
... ‘sickle cell disease’ and ‘Brazil’ over the last five years aiming to provide a current analysis of the subject in ...identified, of which only seven were selected based on the title ... See full document
5
The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease
... Sickle cell disease (SCD) is one of the most common inherited diseases in the world and the patients present notorious clinical ...activation of the blood coagulation and fibrinolytic ... See full document
5
CHARACTERIZATION OF CASES OF SICKLE CELL DISEASE IN A MICROREGION IN THE PIAUI
... cases 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 ... See full document
9
Importance of health guidance for family members of children with sickle cell disease
... mittee of the Universidade Estadual do Ceará (UECE) and the hospital setting of data ...norms of Resolution 466/2012 of the National Health Council (Conselho Nacional de Saúde), the principles ... See full document
9
Professional knowledge of the family health strategy on sickle-cell disease
... quality of life and longevity of individuals with sickle cell ...importance of acquiring new knowledge that will culminate in a care more qualified to relatives and persons suffering ... See full document
11
The pain of children with sickle cell disease: the nursing approach
... Characterization of the nurses participating in the research The participants of this study were 13 nurses, 4 men and 9 women, aged between 23 and 44 years, and service time in pediatric care ranging from 1 ... See full document
7
Incidence of sickle cell disease and other hemoglobin variants in 10,095 Lebanese neonates.
... disorders of hemoglobin (Hb) characterized by the presence of an abnormal b-globin chain (hemoglobin variant as in sickle cell disease) or a decrease or absence of a - or b ... See full document
5
Creation and validation of a health guidance booklet for family members of children with sickle cell disease
... quality of the book, which was confir- med by their reports, where it was noticed that all emphasized that the educational technology clarified many doubts that they possessed, to present a language simpler, along ... See full document
10
Analysis of BCL11A gene polymorphisms and hemolysis parameters in patients with sickle-cell disease
... involvement of the BCL11A gene polymorphism in this region as a modulator of HbF concentration, thus aggravating hemolysis balance in these ...concentration of HbF ... See full document
6
Rev. Bras. Hematol. Hemoter. vol.35 número1
... 21 of 35 sickle cell disease patients presented discrepancies or mismatches for multiple antigens between the genotype proile and the antigen proile of their serologically-matched blood ... See full document
4
Rev. LatinoAm. Enfermagem vol.23 número1
... cause of death among users or not of hydroxyurea with sickle cell ...2010 of patients receiving inpatient treatment in two Brazilian public ...level of significance was p=0.05. ... See full document
7
Assessment of the In Vivo Genotoxicity of New Lead Compounds to Treat Sickle Cell Disease
... lack of mutagenicity of compounds C1–C6 in an in vitro study using a Salmonella/microsome assay ...requirements of these phthalimide derivatives and the mutagenic activity of compounds ... See full document
8
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 ... See full document
6
Rev. Bras. Hematol. Hemoter. vol.34 número4
... complication of sickle cell disease ...years of age with SCD, allowing the identiication of patients at high risk of strokes, such as those with blood low velocities in ... See full document
4
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