Disease | thalassemia |
Phenotype | C0020538|hypertension |
Sentences | 11 |
PubMedID- 21655030 | [12] the incidence of pulmonary hypertension in patients with hbs/β -thalassemia is similar to that observed in patients with scd. |
PubMedID- 26388975 | According to the 60% incidence rate of pulmonary hypertension in patients with thalassemia intermedia, the sample size was calculated to be 60 cases (with a relative accuracy of 25%). |
PubMedID- 24330103 | Prevalence and risk factors for pulmonary hypertension in patients with hemoglobin e/beta-thalassemia disease. |
PubMedID- 22846514 | Determinants of pulmonary hypertension in patients with beta-thalassemia major and normal ventricular function. |
PubMedID- 22075289 | Risk factors for pulmonary hypertension in patients with beta thalassemia intermedia. |
PubMedID- 21705990 | Case report: thalassemia intermedia patient with hypertension non-responsive to combined medical treatment. |
PubMedID- 21712881 | [6] we had used both ibp and cvp monitoring because of severe pulmonary artery hypertension (pah) along with associated thalassemia major in our patient. |
PubMedID- 25170276 | Objective: the aim of the research reported here was to compare pulmonary artery systolic pressure (pasp) and 6-minute walk distance after 1 year of follow-up in hemoglobin e/beta thalassemia (e/beta-thal) with pulmonary arterial hypertension (pah) patients who received chronic blood transfusions versus those who received occasional transfusions. |
PubMedID- 20698879 | Risk factors for pulmonary hypertension in patients with thalassemia intermedia. |
PubMedID- 25386747 | A risk score for predicting pulmonary hypertension in patients with non-transfusion-dependent thalassemia in northeastern thailand: the e-saan score. |
PubMedID- 25621166 | Pulmonary arterial hypertension in a patient with beta-thalassemia intermedia and reversal with infusion epoprostenol then transition to oral calcium channel blocker therapy: review of literature. |
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