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Clinical Classification
Pages 3-11
Punto di Riferimento
per Medici e Operatori Sanitari
per Medici e Operatori Sanitari
LIBRERIA STUDIUM
Diagnosis and Treatment of Pulmonary Hypertension
From Bench to Bedside
Fukumoto
Editore
Springer
Anno
2017
Pagine
236
ISBN
9789812878397
157,00 €
DA SCONTARE
This book focuses on pulmonary arterial hypertension (PAH, Group 1) and chronic thromboembolic pulmonary hypertension (CTEPH, Group 4) among the various groups of pulmonary hypertension (PH) whose classification was updated into five major categories at the 5th World Symposium held in Nice, France, in 2013. Readers will find recent progress, methods, and up-to-date information on PH mechanisms, diagnostic images, and treatment in the management of PH.This volume, with contributions by leading researchers worldwide in the field , consists of five parts, starting with the fundamentals of PH, then pathophysiology and genetics, treatment, and right ventricular function
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Diagnosis: Imaging
Pages 13-27
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Pathogenic and Therapeutic Role of MicroRNA in Pulmonary Arterial Hypertension
Pages 31-54
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Sex Hormones
Pages 55-65
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Rho-Kinase as a Therapeutic Target for Pulmonary Hypertension
Pages 67-76
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The Unique Property of the Pulmonary Artery Regarding the Smooth Muscle Effects of Proteinase-Activated Receptor 1: The Possible Contribution to the Pathogenesis of Pulmonary Hypertension
Pages 77-87
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Animal Models with Pulmonary Hypertension
Pages 89-99
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Human Pathology
Pages 101-113
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Pathophysiology and Genetics: BMPR2
Pages 115-124
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Prostacyclin
Pages 127-138
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Targeting the NO-sGC-cGMP Pathway in Pulmonary Arterial Hypertension
Pages 139-151
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Endothelin Receptor Antagonist
Pages 153-169
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Lung Transplantation
Pages 171-182
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Medical Therapy for Chronic Thromboembolic Pulmonary Hypertension
Pages 185-192
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Balloon Pulmonary Angioplasty
Pages 193-202
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Pulmonary Endarterectomy for Chronic Thromboembolic Pulmonary Hypertension
Pages 203-214
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Right Ventricular Function
Pages 217-236
