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[PDF] Top 20 Renal dysfunction in patients with sickle cell anemia or sickle cell trait

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

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

... children with either Hb SS or Hb AS. It has been reported that patients with Hb SS may present several types of renal dysfunction including hyposthenuria, hema- turia, ... See full document

6

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

S -Haplotypes in sickle cell anemia

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

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

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

... 125 patients with sickle cell anemia (SS) between the ages of 16 to 60 ...Enrolled patients were followed-up pro- spectively for 15 ...severe. Patients with ... See full document

14

Spontaneous miscarriages among sickle cell trait carriers (AS).

Spontaneous miscarriages among sickle cell trait carriers (AS).

... don or samples from Macapá, from patients with varying genders, ages and ethnic origins, wer e collected by ven ou s pu n ctu r e after i n for med ... See full document

4

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

... splenectomized patients who received pneumococcal vaccines and developed severe pneumococcal infections with non-splenectomized patients who were also vaccinated with pneumococcal vaccines and ... See full document

11

Phase 1 study of the E-selectin inhibitor GMI 1070 in patients with sickle cell anemia.

Phase 1 study of the E-selectin inhibitor GMI 1070 in patients with sickle cell anemia.

... elevated in sickle cell disease and mechanistically affected by the target molecule, ...aggregates or PMA); vascular inflammation (soluble E- selectin; soluble ICAM-1); monocyte activation ... See full document

12

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

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

... blood or blood derivative transfusion ...as patients with sickle-cell anemia are at risk for HCV infection, with a prevalence ranging from 2 to 30% (5-11), especially ... See full document

7

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.

... performed in a single center, at the University Hospital of Pointe-à-Pitre (Guadeloupe, French West ...men with SCA who were regularly being followed by the Reference Sickle Cell Center of ... See full document

10

Rev. Bras. Hematol. Hemoter.  vol.35 número3

Rev. Bras. Hematol. Hemoter. vol.35 número3

... kidney dysfunction and haplotypes in sickle cell ...84 sickle cell disease patients, treated in a public health service in Fortaleza, Brazil, was ...57 ... See full document

3

Prevalence of obstructive sleep apnea in children and adolescents with sickle cell anemia

Prevalence of obstructive sleep apnea in children and adolescents with sickle cell anemia

... tive patients with SCA enrolling for treatment at a referral center for hematology and transfu- sion medicine between May of 2007 and May of ...diagnosed with SCA through the quan- titative analysis ... See full document

9

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 ...associated with ... See full document

5

Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia

Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia

... alpha-thalassemia in this study was similar to previous studies in Brazil, with the CAR haplotype being the most common, followed by the BEN ...F or the number of clinical man- ifestations ... See full document

6

Renal tubular dysfunction in sickle cell disease

Renal tubular dysfunction in sickle cell disease

... 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 ... See full document

10

Relationship between ventilation heterogeneity and exercise intolerance in adults with sickle cell anemia

Relationship between ventilation heterogeneity and exercise intolerance in adults with sickle cell anemia

... finding in patients with SCA, mainly among adults ...adults with SCA had restrictive patterns. In SCA, restrictive damage can be explained not only by pulmo- nary structural changes but ... See full document

8

Anestesia em paciente obstétrica portadora de anemia falciforme e traço talassêmico após plasmaféresis: relato de caso

Anestesia em paciente obstétrica portadora de anemia falciforme e traço talassêmico após plasmaféresis: relato de caso

... age, with sickle cell anemia, thalassemic trait and allo-immunization for high fre- quency ...fused with incompatible blood. Patient evolved with massive hemolysis being ... See full document

7

Ultrasound Detection of Salmonella Septic Arthritis in a Rheumatoid Arthritis Patient on Anti-TNF Treatment

Ultrasound Detection of Salmonella Septic Arthritis in a Rheumatoid Arthritis Patient on Anti-TNF Treatment

... reported with anti-TNF ...infection in a psoriatic arthri- tis patient with infliximab ...infection in a RA patient treated with infliximab was ...neutralization with monoclonal ... See full document

5

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

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

... of patients were ...complications in cases of Hb S/D-Punjab and Hb S-Korle Bu disease as well as a reliable evaluation of the late-onset effects of the use of ...children with Hb S- Korle Bu would ... See full document

7

MANAGEMENT OF SICKLE CELL DISEASE

MANAGEMENT OF SICKLE CELL DISEASE

... of Sickle cell anaemia-4, 5, 7, and 11 years of age. The skulls in all cases showed lesions similar to those of erythroblastic ...III. Sickle cell anaemia with unusual bone ... See full document

4

Cerebral Vasculopathy in Children with Sickle Cell Disease

Cerebral Vasculopathy in Children with Sickle Cell Disease

... relevance in the pathophysiology of vasculopathy of all the molecules whose genes were analyzed, the remaining polymorphisms could not be associated to either stroke risk or protection in the present ... See full document

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