• No results found

[PDF] Top 20 Angina Pectoris in a Child With Sickle Cell Anemia

Has 10000 "Angina Pectoris in a Child With Sickle Cell Anemia" found on our website. Below are the top 20 most common "Angina Pectoris in a Child With Sickle Cell Anemia".

Angina Pectoris in a Child With Sickle Cell Anemia

Angina Pectoris in a Child With Sickle Cell Anemia

... A 7-year-old black boy with sickle cell disease, Wolff-Parkinson-White syndrome, mild left ventricular dysfunction, and normal coronary arteries developed angina pectoris five months aft[r] ... See full document

6

Diagnosis at Birth Improves Survival of Children With Sickle Cell Anemia

Diagnosis at Birth Improves Survival of Children With Sickle Cell Anemia

... Diagnosis at Birth Improves Survival of Children With Sickle Cell Anemia. Services[r] ... See full document

6

SALMONELLA OSTEOMYELITIS AND ABNORMAL HEMOGLOBIN DISEASE

SALMONELLA OSTEOMYELITIS AND ABNORMAL HEMOGLOBIN DISEASE

... The second case was reported by Burch6 who described a Negro child with sickle cell anemia and paratyphoid B osteomyelitis. Another case reported by Wigh and Thomp- sonT was in that of a[r] ... See full document

11

Oxidative Modification of Lipids and Lipoproteins in Steady State Sickle Cell Anemic Patients from South-Eastern Nigeria

Oxidative Modification of Lipids and Lipoproteins in Steady State Sickle Cell Anemic Patients from South-Eastern Nigeria

... Abstract: Sickle cell anemia is a genetic disease associated with constant medical ...in sickle cell anemia patients who were in their steady ...with sickle cell ... See full document

5

Dental alterations in sickle cell anemia

Dental alterations in sickle cell anemia

... for sickle crisis makes that in the literature is reported a low caries incidence that subjects without ...In sickle children is described a lower prevalence of caries [9], as a result of an acquisition ... See full document

5

HYPOSTHENURIA IN SICKLE CELL ANEMIA: A REVERSIBLE RENAL DEFECT

HYPOSTHENURIA IN SICKLE CELL ANEMIA: A REVERSIBLE RENAL DEFECT

... THE MAXIMUM SOLUTE CONCENTRATION OF URINE IN THREE CHILDREN WITH SICKLE CELL ANEMIA, ONE CHILD WITH SICKLE CELL HEMOGLOBIN C DISEASE FOLLOWING MULTIPLE TRANSFUSION OF NORMAL RED BLOOD CE[r] ... See full document

11

The Composition and Downward Vertical Transport of Particulate Phosphorus in the Cariaco Basin, Venezuela

The Composition and Downward Vertical Transport of Particulate Phosphorus in the Cariaco Basin, Venezuela

... of anemia, higher hematocrit is associated with a higher pain rate and a shorter duration between pain episodes (Dampier, Ely, Brodecki, & O'Neal, 2002; Platt, et ...with sickle cell ... See full document

172

GSTT1 null genotype in sickle cell anemia and blood transfusion recurrence – a case report

GSTT1 null genotype in sickle cell anemia and blood transfusion recurrence – a case report

... Patients with SCA suffer from acute and chronic vaso-occlusive seizures. These physiopathological events of SCA lead to a variety of morbidities such as pain, acute thoracic syndrome, stroke, aseptic necrosis of the ... See full document

5

AUREOMYCIN IN STAPHYLOCOCCIC MENINGITIS COMPLICATING SUBARACHNOID HEMORRHAGE IN SICKLE CELL ANEMIA

AUREOMYCIN IN STAPHYLOCOCCIC MENINGITIS COMPLICATING SUBARACHNOID HEMORRHAGE IN SICKLE CELL ANEMIA

... SUBARACHNOID HEMORRHAGE IN SICKLE CELL ANEMIA AUREOMYCIN IN STAPHYLOCOCCIC MENINGITIS COMPLICATING. Services[r] ... See full document

7

Glucose 6 phosphate dehydrogenase deficiency and hemoglobinopathy in South Western Region Nepal: a boon or burden

Glucose 6 phosphate dehydrogenase deficiency and hemoglobinopathy in South Western Region Nepal: a boon or burden

... of anemia was not milder in G6PD deficiency than in G6PD normal patients but could not be proved to be significantly more severe ...neither anemia nor evidence of increased RBC destruction, nor an ... See full document

6

Nonconventional therapeutic modalities in refractory angina pectoris

Nonconventional therapeutic modalities in refractory angina pectoris

... the cell injection had received a coronary artery bypass graft ...marrow-derived cell type and even the cell isolation procedure will ultimately depend greatly on the cardiac injury to be ...stem ... See full document

9

Pulmonary hypertension in Nigerian adults with sickle cell anemia

Pulmonary hypertension in Nigerian adults with sickle cell anemia

... chronic anemia, while the association with a lower PCV may be due to the effect of cell-free hemoglobin resulting from chronic hemolysis on nitric oxide ... See full document

8

OXYGEN DISSOCIATION CURVES IN SICKLE CELL ANEMIA AND IN SUBJECTS WITH THE SICKLE CELL TRAIT

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

6

ISSUES TO BE CONSIDERED

ISSUES TO BE CONSIDERED

... screening laws can accommodate sickle cell anemia, the malpractice concerns related to sickle cell ane- mia screening, the need for protection of the con- fidentiality of the data collec[r] ... See full document

7

A Meta-analysis of Effectiveness Evaluation between Shexiang Baoxin Pill and Isosorbide Mononitrate Tablet

A Meta-analysis of Effectiveness Evaluation between Shexiang Baoxin Pill and Isosorbide Mononitrate Tablet

... unstable angina or stable angina pectoris) and (Shexiang Baoxin Pill) and (xinkang or isosorbide mononitrate tablet or isosorbide-5-nitrate tablet or isosorbide-5-nitrate tablet), due to the need of ... See full document

6

Exercise induced hemolysis in xerocytosis  Erythrocyte dehydration and shear sensitivity

Exercise induced hemolysis in xerocytosis Erythrocyte dehydration and shear sensitivity

... susceptible than normal erythrocytes to hemolysis by shear stress. Fractionation of normal and abnormal cells on discontinuous Stractan density gradients revealed that increasingly dehydrated cells were increasingly more ... See full document

9

Sickle Cell Beta Thalassemia: A Rare Entity

Sickle Cell Beta Thalassemia: A Rare Entity

... during acute severe exacerbations of anemia, as during splenic crisis or aplastic crises. Chelation therapy can be administered with iron chelators such as deferoxamine, deferasirox, and deferiprone to reduce the ... See full document

6

STUDIES IN SICKLE CELL ANEMIA

STUDIES IN SICKLE CELL ANEMIA

... segregate the cases of sickle cell anemia from those subjects bearing only the sick- ling trait.. Table II summarizes the sex incidence of subjects bearing the asympto-.[r] ... See full document

8

STUDIES IN SICKLE CELL ANEMIA

STUDIES IN SICKLE CELL ANEMIA

... AV. Volume of blood and mass of hemoglobin in patients with crises of sickle cell anemia. Both. dextran and whole blood effected increases in circulating mass of hemoglobin which could n[r] ... See full document

12

STUDIES IN SICKLE CELL ANEMIA

STUDIES IN SICKLE CELL ANEMIA

... comprehensive reviews2636 of the cerebral manifestations and pathological findings as- sociated with sickle cell disease appeared in the medical literature. Our data and the observations[r] ... See full document

11

Show all 10000 documents...