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Libreria medica internazionale
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Idiopathic Pulmonary Fibrosis
A Comprehensive Clinical Guide
Meyer, Nathan
Editore
Springer
Anno
2019
Pagine
475
ISBN
9783319999746
160,00 €

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I prezzi indicati possono subire variazioni poiché soggetti all'oscillazione dei cambi delle valute e/o agli aggiornamenti effettuati dagli Editori.

This book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management. Since the first edition, many new developments have occurred in the understanding and management of this serious disease, revising our understanding of how it presents, manifests, and reacts to certain treatments. This second edition is fully updated with six new chapters by our team of international, expert authors. New topics include: classification of interstitial lung disease, pulmonary function tests in IPF, biomarkers, clinical phenotypes, mimics, and a discussion of clinical trials. Each chapter additionally includes a brief summary of ongoing research and potential future directions. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide, Second Edition is an invaluable resource for clinicians who desire a deeper understanding of IPF in order to better help their patients.

  • Classification and Nomenclature of Interstitial Lung Disease

    Meyer, Keith C.

    Pages 1-10

  • Idiopathic Pulmonary Fibrosis: The Epidemiology and Natural History of Disease

    Mohning, Michael P. (et al.)

    Pages 11-35

  • Histopathology of IPF and Related Disorders

    Lagstein, Amir (et al.)

    Pages 37-60

  • Imaging of Idiopathic Pulmonary Fibrosis

    Chung, Jonathan H. (et al.)

    Pages 61-83

  • Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis

    Bonella, Francesco (et al.)

    Pages 85-95

  • The Role of Immunity and Inflammation in IPF Pathogenesis

    Butler, Marcus W. (et al.)

    Pages 97-131

  • Mechanisms of Fibrosis in IPF

    Sandbo, Nathan

    Pages 133-182

  • Genetics of Pulmonary Fibrosis

    Adams, Traci N. (et al.)

    Pages 183-206

  • Evolving Genomics of Pulmonary Fibrosis

    Ibarra, Gabriel (et al.)

    Pages 207-239

  • Biomarkers in Idiopathic Pulmonary Fibrosis

    Sood, Shweta (et al.)

    Pages 241-271

  • Idiopathic Pulmonary Fibrosis: Phenotypes and Comorbidities

    King, Christopher S. (et al.)

    Pages 273-297

  • The Keys to Making a Confident Diagnosis of IPF

    Sheth, Jamie (et al.)

    Pages 299-323

  • Pharmacologic Treatment of IPF

    Smargiassi, Andrea (et al.)

    Pages 325-364

  • Mimics of Idiopathic Pulmonary Fibrosis

    Meyer, Keith C. (et al.)

    Pages 365-378

  • Gastroesophageal Reflux and IPF

    Lee, Joyce S.

    Pages 379-387

  • The Role of Pulmonary Rehabilitation and Supplemental Oxygen Therapy in the Treatment of Patients with Idiopathic Pulmonary Fibrosis

    Wittman, Catherine (et al.)

    Pages 389-399

  • Acute Exacerbation of Idiopathic Pulmonary Fibrosis

    Lee, Joyce S. (et al.)

    Pages 401-417

  • Lung Transplantation for Idiopathic Pulmonary Fibrosis

    Lamas, Daniela J. (et al.)

    Pages 419-432

  • Clinical Trials in IPF: What Are the Best Endpoints?

    Spagnolo, Paolo (et al.)

    Pages 433-453

  • Future Directions for IPF Research

    Craig, J. Matt (et al.)

    Pages 455-467

 

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