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Demographic and clinical characteristics of pulmonary arterial hypertension caused by schistosomiasis are indistinguishable from other etiologies

INTRODUCTION: Pulmonary arterial hypertension (PAH) is a serious pulmonary circulation disease caused by several etiologies, including schistosomiasis. The present study retrospectively evaluated the clinical and hemodynamic characteristics of patients with schistosomal PAH (PAH-Sch) compared to tho...

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Bibliografiska uppgifter
I publikationen:Rev Soc Bras Med Trop
Huvudupphovsmän: Mendes, Adriano Assis, Roncal, Carlos Guilhermo Piscoya, de Oliveira, Flávio Roberto Azevedo, de Albuquerque, Eugênio Soares, Góes, Gustavo Henrique Belarmino, Piscoya, Isabelle Cecília de Vasconcellos, Sobral, Dário Celestino
Materialtyp: Artigo
Språk:Inglês
Publicerad: Sociedade Brasileira de Medicina Tropical - SBMT 2020
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7083352/
https://ncbi.nlm.nih.gov/pubmed/32049203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/0037-8682-0418-2019
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