Pulmonary hypertension in thalassemia: a call to action
Author:
Affiliation:
1. Children’s Hospital of Los Angeles
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
https://ashpublications.org/blood/article-pdf/139/13/1937/1884283/bloodbld2021015340c.pdf
Reference10 articles.
1. Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization;Pinto;Blood.,2022
2. Prevalence and risk factors for pulmonary arterial hypertension in a large group of β-thalassemia patients using right heart catheterization: a Webthal study;Derchi;Circulation.,2014
3. Therapy for pulmonary arterial hypertension in adults: update of the CHEST guideline and expert panel report;Klinger;Chest.,2019
4. Effect of genotype on pulmonary hypertension risk in patients with thalassemia;Teawtrakul;Eur J Haematol.,2014
5. Cardiac status in well-treated patients with thalassemia major;Aessopos;Eur J Haematol.,2004
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3. Macitentan Administration for Pulmonary Hypertension Due to β-thalassemia with Multiple Organ Failure: A Case Report;Internal Medicine;2024
4. Extramedullary hematopoiesis in ribs and severe pulmonary hypertension disease following intermediate beta-thalassemia: a case report;Journal of Medical Case Reports;2023-12-09
5. Cardiac complications in thalassemia throughout the lifespan: Victories and challenges;Annals of the New York Academy of Sciences;2023-10-30
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