Pulmonary Arterial Hypertension in a Patient with β‐Thalassemia Intermedia and Reversal with Infusion Epoprostenol Then Transition to Oral Calcium Channel Blocker Therapy: Review of Literature-Reference-Cited by-同舟云学术

Pulmonary Arterial Hypertension in a Patient with β‐Thalassemia Intermedia and Reversal with Infusion Epoprostenol Then Transition to Oral Calcium Channel Blocker Therapy: Review of Literature

Published:2014-09 Issue:3 Volume:4 Page:520-526
ISSN:2045-8940
Container-title:Pulmonary Circulation
language:en
Short-container-title:Pulm. circ.

Author:

Ussavarungsi Kamonpun¹,Burger Charles D.¹

Affiliation:

1. Pulmonary and Critical Care MedicineMayo ClinicJacksonvilleFloridaUSA

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1086/677367

Reference25 articles.

1. Pulmonary hypertension in thalassemia;Morris CR;Ann N Y Acad Sci,2010

2. Thalassemia heart disease: A comparative evaluation of thalassemia major and thalassemia intermedia;Aessopos A;Chest,2005

3. Risk factors for pulmonary hypertension in patients with β thalassemia intermedia;Karimi M;Eur J Intern Med,2011

4. Pulmonary hypertension in thalassaemia major patients with normal left ventricular systolic function;Hagar RW;Br J Haematol,2006

5. Pulmonary hypertension associated with hemoglobinopathies: Prevalent but overlooked;Farmakis D;Circulation,2011

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4. The wide spectrum of β‐thalassaemia intermedia‐induced pulmonary hypertension: two case reports on the possible role of specific pulmonary arterial hypertension therapy;Pulmonary Circulation;2021-07

5. Thalassemia Associated Pulmonary Hypertension;Iranian Journal of Pediatric Hematology & Oncology;2020-12-29