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Sickle Cell Trait

Renal dysfunction in patients with sickle cell anemia or sickle cell trait

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 ...

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Confidencialidade, aconselhamento genético e saúde pública: um estudo de caso sobre o traço falciforme Confidentiality, genetic counseling, and public health: a case study on sickle cell trait

Confidencialidade, aconselhamento genético e saúde pública: um estudo de caso sobre o traço falciforme Confidentiality, genetic counseling, and public health: a case study on sickle cell trait

... Por meio de um estudo etnográfi- co sobre o aconselhamento genético ministrado às pes- soas identificadas como portadoras do traço falcifor- me em um dos principais centros de doação de [r] ...

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J. Bras. Patol. Med. Lab.  vol.51 número4

J. Bras. Patol. Med. Lab. vol.51 número4

... This study showed higher rates of sickle cell trait in Afro Brazilians, which conirms data published in other Brazilian regions and states. Therefore, taking into account the miscegenation and the ...

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Renal tubular dysfunction in sickle cell disease

Renal tubular dysfunction in sickle cell disease

... This is a prospective cohort study with 26 consecutive patients with clinical and laboratory diagnosis of SCD (hemoglobin SS) undergoing consultation in a public health service in Brazil from December 2010 to June 2012. ...

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Int. braz j urol.  vol.33 número5

Int. braz j urol. vol.33 número5

... with sickle cell ...seventh sickle cell nephropathy. The six sickle cell nephropathies previously described by Berman (2), in 1974, are gross hematuria, papillary necrosis, ...

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Maternal anaemia at delivery and haemoglobin evolution in children during their first 18 months of life using latent class analysis.

Maternal anaemia at delivery and haemoglobin evolution in children during their first 18 months of life using latent class analysis.

... of sickle cell trait among ...and sickle cell) we can argue that the sickle cell trait effect is independent of the protection against clinical malaria classically ...

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S -Haplotypes in sickle cell anemia

S -Haplotypes in sickle cell anemia

... Sickle cell disease affects millions world- wide, and occurs in one of every 500 Afri- can-American births, and in one of every 1000 to 4000 Hispanic-American ...the sickle cell trait ...

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Rev. Bras. Hematol. Hemoter.  vol.38 número3

Rev. Bras. Hematol. Hemoter. vol.38 número3

... the sickle cell trait, but caution should be taken with this statement, considering the limited number of children and short follow-up thus far ...

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J. Bras. Patol. Med. Lab.  vol.49 número4

J. Bras. Patol. Med. Lab. vol.49 número4

... with sickle cell trait, including two males and two ...of sickle cell trait was similar to that reported in the general adult population of the state of Rio de Janeiro (4% by ...

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Sickle cell disease and associated problems: Case study of  Homozygous sicklers

Sickle cell disease and associated problems: Case study of Homozygous sicklers

... This paper is focused on the problems faced by homozygous individuals of sickle cell disease. In a survey of 500 household of 17 villages of district Mandla, a total of 2316 individuals were covered out of ...

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Self-care of men with priapism and sickle cell disease

Self-care of men with priapism and sickle cell disease

... of sickle cell disease, based on the reports of the participants of this study, led to the conclusion that there is still a deficiency in professional training regarding the disease and its complications ...

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Comparison of oxidative stress and the frequency of polymorphisms in the HFE gene between hemoglobin S trait blood donors and sickle cell disease patients

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 sickle cell disease patients with the HFE mutation to the sickle cell patients without it, we veriied that there was no sig- niicant difference between these two groups of patients ...

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Cerebral Vasculopathy in Children with Sickle Cell Disease

Cerebral Vasculopathy in Children with Sickle Cell Disease

... 2004). Sickle RBCs are more sensitive to these aggressions due to the membrane damages that occur during ...of sickle erythrocytes, they get stuck in splenic sinusoids much more frequently than normal RBCs, ...

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Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength.

Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength.

... The pathophysiology of SCA-related priapism remains only partially understood. Initially, low-flow (ischemic) priapism, which is the form of this complication typically associated with SCA, was presumed to result from ...

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Mobile applications for sickle cell disease management: an integrative review

Mobile applications for sickle cell disease management: an integrative review

... Cell Disease (doença falciforme), smartphones, cell phones (telefones celulares), mobile applications (aplicativos móveis), Educational technology (tec- nologia educacional). For the query, the association ...

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Risk factors for alloimmunization by patients with sickle cell disease

Risk factors for alloimmunization by patients with sickle cell disease

... A significant association between Hb phenotype and alloimmunization was ob- served even after multivariate adjustment in patients older than14 years. Patients with Hb SC presented a risk of alloimmunization al- most ...

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Hepatitis C virus infection in a Brazilian population with sickle-cell anemia

Hepatitis C virus infection in a Brazilian population with sickle-cell anemia

... red cell concentrate or other blood deriva- tives since the time of registration with the Hospital of the HEMOPE Foundation or when they reported transfusion at another ...

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The pain of children with sickle cell disease: the nursing approach

The pain of children with sickle cell disease: the nursing approach

... Objective: To describe how nurses identify the pain in children with sickle cell disease (SCD) and to list the strategies used by them in the evaluation and control of pain. Method: This is a qualitative, ...

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Fatores de risco para aloimunização em pacientes com anemia falciforme

Fatores de risco para aloimunização em pacientes com anemia falciforme

... Transfusion therapy with packed red blood cells (PRBCs) is a common practice in the treatment and prevention of complications in sickle cell anemia (SS). Approximately 50% of patients with SS receive ...

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