[PDF] Top 20 A pesquisa em arquivística na pós-graduação no Brasil : balanço e perspectivas
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Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis
... higher risk of VTE and specifically PE as- sociated with SCT in the general ...greater risk of VTE in individuals of Afri- can descent compared to Caucasians ...increased risk of VTE in pregnant or ... See full document
12
Risk of venous thromboembolism in patients with cancer: a systematic review and meta analysis
... Our systematic review and meta-analysis has several ...a review of the literature on this important topic has attempted to quantify precisely the likelihood of this potentially ... See full document
15
Venous thromboembolism in adults screened for sickle cell trait: a population-based cohort study with nested case–control analysis
... higher risk of PE among hospitalised black Americans with SCT, with no increased risk of DVT in carriers compared with ...overall risk of VTE but up to a twofold increased risk of ...increased ... See full document
14
Venous thromboembolism in adults screened for Sickle Cell Trait: a population based cohort study with nested case control analysis
... higher risk of PE among hospitalised black Americans with SCT, with no increased risk of DVT in carriers compared with ...overall risk of VTE but up to a twofold increased risk of ...increased ... See full document
63
Glucose 6 phosphate dehydrogenase deficiency and hemoglobinopathy in South Western Region Nepal: a boon or burden
... Though exact data regarding the spectrum of hemoglo- binopathy in Nepal is not known, it seems to be increas- ing. If disease continues to pass vertically, it may take the form of epidemic. This study has provided ... See full document
6
Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC)
... the disease is relatively simple, and mandatory newborn screening for SCD exists in all states so such interventions can be initiated early in the lifespan ... See full document
11
SICKLE CELL DISEASE- AN AYURVEDIC PERSPECTIVE .......
... Sickle cell disease or Sickle cell anemia is a genetic disease seen amongst various tribal populations of India that affects the ...hemoglobin. Sickle cell anemia ... See full document
5
ANESTHETIC RISKS IN SICKLE CELL TRAIT
... Most clinical disease associated with sick- ling of red blood cells has been described in sickle cell anemia ( S-S hemoglobinopathy),. sickle cell-hemoglobin C disease ( S-C hemo-[r] ... See full document
13
FILTER PAPER ELECTROPHORESIS OF HUMAN HEMOGLOBIN
... In addition to its usefulness in the detection of other abnormal hemoglobins, filter paper electrophoresis has been a valuable aid in distinguishing sickle cell trait from sickle cell an[r] ... See full document
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Immunological Characterization in Malaria Patients with and without the Sickle Cell Trait
... blood cell polymorphisms are frequently in zone where malaria is endemic so, some of these polymor- phisms may give a relative advantage for survival ...The sickle cell trait (HbAS), ... See full document
69
Hydroxyurea for Sickle Cell Disease: A Systematic Review for Efficacy and Toxicity in Children
... RESULTS. We included 26 articles describing 1 randomized, controlled trial, 22 obser- vational studies (11 with overlapping participants), and 3 case reports. Almost all study participants had sickle cell ... See full document
7
OXYGEN DISSOCIATION CURVES IN SICKLE CELL ANEMIA AND IN SUBJECTS WITH THE SICKLE CELL TRAIT
... Table I indicates that despite efforts to keep the pCO2 constant in all studies, the mean pCO2 for the experimental points calculated in the cases of sickle cell anemia was higher than t[r] ... See full document
48
PATHOGENESIS OF HYPOSTHENURIA IN PERSONS WITH SICKLE CELL ANEMIA OR THE SICKLE CELL TRAIT
... over 6 months of age have hyposthenunia; 2) hyposthenuria becomes increasingly more severe with advancing age in both sickle cell anemia and sickle cell trait; 3) in a 6-month-old patien[r] ... See full document
58
The Effect of Hydroxyurea Treatment on Fetal Haemoglobin Level and Clinical Status of Sudanese Sickle Cell Anaemia Patients
... Sudanese sickle cell anaemia, this can be attributed to many factors reported to influence the response to hydroxurea treatment such as the baseline level of Hb-F as the higher response of Hb-F level has ... See full document
88
Current challenges in the management of patients with sickle cell disease – A report of the Italian experience
... a disease of children, with few surviving to adulthood ...intensive disease management, more than 95% of chil- dren with SCD in developed countries reach adulthood ... See full document
8
Combination of Haemoglobinopathy and Haemopathy —(Adult T Cell Lymphoma/Leukemia and Sickle Cell Disease: A Rare Case of Disease Observed in the Adult Referral Center of Sickle Cell Disease (CRD A) in Martinique
... Authors report a case of beta thalassemia combined with hematological ma- lignant (ATLL) in a 40-year-old female, cashier screened HTLV-1 positive; followed since her 10 years old for the account of ... See full document
13
Comparative Study between Cholecystectomy in Sickle Cell Patients and Non Sickle Cell Patients
... in sickle cell patients and 33 cases in non-sickle cell ...for sickle cell patients. They were found in 11 cases in non-sickle cell ...the sickle cell ... See full document
143
Cutaneous Manifestations of Sickle Cell Disease
... of Sickle Cell Disease (CSSCD) found that about 25% of patients with SCD over the age of ten had a history of leg ulcers, with active ulcers at entry or development of ulcers during the eight year ... See full document
110
Trait Anxiety in Sickle Cell Disease: investigating and exploring links to the management of pain
... Both participants reported that they experienced pain all of the time and expressed that stress exacerbated their pain. Findings by Anie et al. (2012) support this finding. Anie et al. (2012) showed that mood levels ... See full document
20
Preventing Inappropriate Hydroxyurea Dosing in Children by Introducing a Child-Appropriate Preparation
... when there are no apparent symptoms. These conditions have been shown to adversely affect adherence. Adherence has been shown to be low if a key family member or the child is not supportive of the treatment with HU [2]. ... See full document
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