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[Hypoglycemia in a patient with pleural solitary fibrous tumor and response to pasireotide] [PDF]
Videla EK+6 more
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[Phosphodiesterase 5 inhibitors for the treatment of heart failure: a systematic review and meta-analysis]. [PDF]
Monzón-Herrera R+3 more
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Electrocardiographic Prognostic Marker in Pulmonary Arterial Hypertension: RS Time. [PDF]
Koyun E+5 more
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Morfotopografia y patogenia del infarto hemorrágico encefálico en la hipertensión arterial [PDF]
Pons Tortella, E.
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Hipertensión arterial pulmonar: Nuevas variantes patogénicas se detectan el nuevo panel genético
Kompass Neumología, 2022Background: A genetic predisposition can lead to the rare disease pulmonary arterial hypertension (PAH). Most mutations have been identified in the gene BMPR2 in heritable PAH. However, as of today 15 further PAH genes have been described.
Marco Hugo Sánchez-Bustillos
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Revista Colombiana de Neumología
Introduction: Pulmonary Arterial Hypertension (PAH) is a clinical condition characterized by dysfunction of the pulmonary arterial endothelium that manifests with increased flow restriction in the pulmonary circulation.
Manuel Conrado Pacheco Gallego+36 more
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Introduction: Pulmonary Arterial Hypertension (PAH) is a clinical condition characterized by dysfunction of the pulmonary arterial endothelium that manifests with increased flow restriction in the pulmonary circulation.
Manuel Conrado Pacheco Gallego+36 more
semanticscholar +1 more source